Search Result
Results for "
FMoc
" in MedChemExpress (MCE) Product Catalog:
14
Biochemical Assay Reagents
76
Isotope-Labeled Compounds
Cat. No. |
Product Name |
Target |
Research Areas |
Chemical Structure |
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- HY-W052227
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- HY-W007052
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- HY-W013152
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- HY-W048682
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Amino Acid Derivatives
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Others
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Fmoc-1-methyl-L-histidine is a Fmoc protected amino acid and can be used as an intermediate for peptide synthesis .
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- HY-148339
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Drug-Linker Conjugates for ADC
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Others
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Fmoc-VAP-MMAE is a agent-linker conjugates for ADC. Fmoc-VAP-MMAE consists of an ADC linker and a tubulin inhibitor MMAE (HY-15162), with a protective Fmoc group .
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- HY-78933
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Microtubule/Tubulin
ADC Cytotoxin
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Cancer
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Fmoc-MMAE is a protective group-conjugated monomethyl auristatin E (MMAE), which is a potent tubulin inhibitor. Fmoc-MMAE can be used in the synthesis of ADC .
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- HY-P2392
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- HY-W013123
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Amino Acid Derivatives
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Others
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Fmoc-D-Phe(4-CF3)-OH is Phenylalanine derivative. Fmoc-D-Phe(4-CF3)-OH can be used for the research of peptide inhibitors of protein-protein interactions .
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- HY-W010712
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Amino Acid Derivatives
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Others
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Fmoc-His(Trt)-OH has trityl (Trt) group to protect the side-chain of His. Fmoc-His(Trt)-OH has Fmoc group to protect -αNH2. Fmoc-His(Trt)-OH can be used for solid phase synthesis of peptides, providing protection against racemization and by-product formation .
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- HY-41189
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ADC Linker
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Cancer
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Fmoc-Val-Cit-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Val-Cit-PAB-PNP has superior plasma stability comparable to that of non-cleavable linkers .
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- HY-Y1636
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Amino Acid Derivatives
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Others
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Fmoc-Arg(Pbf)-OH is an arginine derivative containing amine protecting group Fmoc. Fmoc-Arg(Pbf)-OH is a building block for the introduction of Arg into SPPS (Solid-Phase Peptide Synthesis) .
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- HY-W072147
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FMoc-L-Ser-OMe
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Amino Acid Derivatives
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Others
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Fmoc-Ser-OMe (Fmoc-L-Ser-OMe) is a hydroxylated L-amino acid protected with a 9-fluorenylmethyloxycarbonyl (Fmoc) group. Fmoc-Ser-OMe involves in chlorophyll–amino acid conjugates synthesis, and acts as a chromo/fluorophores modified protein and emits visible to near-infrared lights efficiently. Fmoc-Ser-OMe glycosylates and produces small mucin-related Olinked glycopeptides, as an alcohol acceptor .
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- HY-W008386
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- HY-W013083
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- HY-W013750
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- HY-W022255
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D-FMoc-glutamic acid
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Amino Acid Derivatives
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Others
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Fmoc-D-Glu-OH (D-Fmoc-glutamic acid) is a derivative of glutamate, can be used to prepare supramolecular hydrogels .
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- HY-W142161
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FMoc-MeHis(Trt)-OH
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Amino Acid Derivatives
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Others
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Fmoc-N-Me-His(Trt)-OH (Fmoc-MeHis(Trt)-OH) is a is an amino acid derivative containing amino and carboxyl groups. Fmoc-N-Me-His(Trt)-OH for the synthesis of Fmoc-MeHis (Trt) -Leu-OH .
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- HY-I1111
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- HY-W048674
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FMoc-O-acetyl-L-serine
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Amino Acid Derivatives
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Infection
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Fmoc-Ser(Ac)-OH (Fmoc-O-acetyl-L-serine) is a Serine derivative. Fmoc-Ser(Ac)-OH can be used for the preparation of broad-spectrum coronavirus membrane fusion inhibitor .
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- HY-101064S3
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PPAR
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Fmoc-leucine-d10 is the deuterium labeled Fmoc-leucine. Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity in normal, diet-induced glucose-intolerant, and in diabetic db/db mice. Fmoc-leucine has a lower adipogenic activity[1].
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- HY-W048209
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Amino Acid Derivatives
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Others
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Fmoc-Lys(Palmitoyl)-OH is a Fmoc-amino acid with long alkyl chains. Fmoc-Lys(Palmitoyl)-OH can be used for peptide synthesis .
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- HY-19821
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FMoc-L-isoleucine
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Fmoc-Ile-OH is an isoleucine derivative .
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- HY-W010895
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- HY-W013162
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- HY-W010893
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- HY-W011020
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- HY-79255
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ADC Cytotoxin
Microtubule/Tubulin
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Cancer
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Fmoc-MMAF-OMe is an anticancer agent and tubulin polymerization inhibitor with an Fmoc protecting group. The active ingredient of Fmoc-MMAF-OMe, MMAF (HY-15579), is the cytotoxic (ADC Cytotoxin) component of classic antibody drug conjugates (ADCs) .
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- HY-22295
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Biochemical Assay Reagents
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Others
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Fmoc-4-aminobutanoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-Y1250S5
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- HY-19821S
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- HY-79131S5
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- HY-W022223
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- HY-W007713
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FMoc-NH-PEG2-CH2COOH
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ADC Linker
PROTAC Linkers
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Cancer
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Fmoc-8-amino-3,6-dioxaoctanoic acid (Fmoc-NH-PEG2-CH2COOH) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-8-amino-3,6-dioxaoctanoic acid is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-W011021
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- HY-W010756
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- HY-W009034
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Others
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Others
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Fmoc-Suberol is a protein cross-linking agent.
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- HY-151640
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ADC Linker
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Others
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Fmoc-DAP-N3 is a click chemistry reagent containing an azide group. Fmoc-DAP-N3 is a short, linear spacer molecule with Fmoc protected amino function. Fmoc-DAP-N3 can be used in click conjugation and amid bond formation either with small molecules or for bioconjugation with proteins and antibodies .
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- HY-101064
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N-FMoc-leucine; NPC 15199; NSC 334290
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Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity in normal, diet-induced glucose-intolerant, and in diabetic db/db mice. Fmoc-leucine has a lower adipogenic activity .
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- HY-W009204S5
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Isotope-Labeled Compounds
PPAR
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Metabolic Disease
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Fmoc-Ala-OH- 13C3 is a 13C-labeled Fmoc-leucine. Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity in normal, diet-ind
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- HY-79131S4
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- HY-W007720S
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- HY-W007720S1
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- HY-W008371S2
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- HY-W009204S8
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- HY-W013780S3
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- HY-W002327
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Biochemical Assay Reagents
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Others
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Fmoc-Asn(Trt)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Fmoc-Asn(Trt)-OH can be used for synthesis of Fmoc-based solid-phase peptide synthesis .
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- HY-W041988
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Bacterial
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Infection
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Fmoc-Glu-OMe, a glutamic acid derivative, shows antibacterial activity and gelation property in AgNO3 solution. Fmoc-Glu-OMe is a mouldable wound healing biomaterial .
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- HY-78921
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ADC Linker
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Cancer
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Fmoc-3VVD-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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- HY-W052227S
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- HY-19811
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- HY-I1111S
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- HY-W009204S
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- HY-W008371S
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- HY-Y1250S
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- HY-79131S2
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- HY-W009204S6
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- HY-W142064
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Antibiotic
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Others
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Fmoc-L-photo-proline is a photo-crosslinking amino acid which can be incorporated into synthetic peptides using solid-phase Fmoc chemistry. Fmoc-L-photo-proline can synthesis of cyclic peptidomimetic antibiotic and be used for preparation of diverse peptide-based photoaffinity probes research .
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- HY-W048825
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Amino Acid Derivatives
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Others
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Fmoc-Ala-Ala-OH (3) is a self-assemble fluorenylmethoxycarbonyl-dipeptide, which is a smaller amphiphilic building blocks consists dipeptides linked to fluore nylmethoxycarbonyl (Fmoc). Fmoc-Ala-Ala-OH can be used as scaffold materials in 3D cell culture .
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- HY-W008688
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- HY-W011084
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- HY-19318G
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ADC Linker
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Cancer
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Fmoc-Val-Cit-PAB GMP is a GMP grade Fmoc-Val-Cit-PAB (HY-19318). Fmoc-Val-Cit-PAB is a cleavable antibody-conjugated active molecule (ADC) commonly used linker.
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- HY-W008235
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- HY-W008558
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- HY-Y1250S3
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- HY-151638
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ADC Linker
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Others
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FMOC-3-azido-D-alanine is a click chemistry reagent containing an azide group .
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- HY-148462
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ADC Linker
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Cancer
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Fmoc-Ala-Ala-PAB is a cleavable ADC linker. Fmoc-Ala-Ala-PAB can be used in the synthesis of antibody-drug conjugates (ADCs) .
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- HY-46398
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PROTAC Linkers
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Cancer
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Fmoc-Val-Phe-Boc is a PROTAC linker and a maleimide-GGFG peptide linker. Fmoc-Val-Phe-Boc can be used in the synthesis of the Deruxtecan .
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- HY-W007941S1
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- HY-W010758
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- HY-W010975
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ADC Linker
PROTAC Linkers
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Cancer
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Fmoc-Lys-OH hydrochloride is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Lys-OH hydrochloride is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-W013190
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- HY-W009003
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- HY-W009005
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- HY-W009085
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- HY-W009088
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- HY-W010793
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- HY-W007020
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- HY-W007720
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- HY-W008176
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- HY-W008475
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- HY-W008696
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- HY-W041982
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- HY-W010959
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- HY-W011000
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- HY-W011081
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- HY-W011135
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- HY-W008360
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- HY-W041991
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- HY-W141948
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- HY-79648
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- HY-79131
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- HY-W019028
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- HY-22297
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- HY-W009204
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- HY-W009151
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- HY-W013780
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- HY-101064S1
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Isotope-Labeled Compounds
PPAR
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Metabolic Disease
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Fmoc-leucine- 13C6, 15N is a 15N-labeled and 13C-labled Fmoc-leucine. Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity
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- HY-W007798S1
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Isotope-Labeled Compounds
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Others
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Fmoc-Cys(Trt)-OH-d2 is the deuterium labeled Fmoc-Cys(Trt)-OH. Fmoc-Cys(Trt)-OH is an N-terminal protected cysteine derivative[1].
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- HY-151637
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Amino Acid Derivatives
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Others
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Fmoc-N-propargyl-MPBA is a propargyl-substituted MPBA linker derived from 4-hydroxy-3-methoxybenzaldehyde. Fmoc-N-propargyl-MPBA can be elongated using standard Fmoc-based solid phase chemistry and linked to supports by standard coupling procedures . Fmoc-N-propargyl-MPBA is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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- HY-79128
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FMoc-L-Lys(Boc)-OH; FMoc-Lys(Boc)-OH; N-α-(FMoc)-N-ε-(t-boc)-L-Lysine-OH
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Amino Acid Derivatives
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Others
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Fmoc-L-Lys (Boc)-OH is a lysine derivative .
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- HY-78921AG
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ADC Linker
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Cancer
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Fmoc-3VVD-OH (GMP) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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- HY-W008072S
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- HY-W011026S
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- HY-W011026S1
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- HY-W011002
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- HY-W010880
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- HY-W016032
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- HY-W008205
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FMoc-L-Hydroxyproline
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Biochemical Assay Reagents
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Others
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Fmoc-Hyp-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-134517
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Amino Acid Derivatives
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Others
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Fmoc-HoCys(ACM)-OH, a homolog of cysteine, is synthesized from L-methionine. Fmoc-HoCys(ACM)-OH also can be used for the synthesis of solid phase peptide .
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- HY-W048671
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Amino Acid Derivatives
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Others
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Fmoc-Thr(TBDMS)-OH is a Threonine derivative. Fmoc-Thr(TBDMS)-OH can be used for the preparation of sugar ligand-tethered functional nucleic acid conjugates for targeted research .
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- HY-W010712S1
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Isotope-Labeled Compounds
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Others
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Fmoc-His(Trt)-OH- 15N3 is the 15N labeled Fmoc-His(Trt)-OH[1]. Fmoc-His(Trt)-OH has trityl (Trt) group to protect the side-chain of His. Fmoc-His(Trt)-OH has Fmoc group to protect -αNH2. Fmoc-His(Trt)-OH can be used for solid phase synthesis of peptides, providing protection against racemization and by-product formation[2].
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- HY-103664
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- HY-W048688
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Amino Acid Derivatives
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Others
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Fmoc-Trp(Me)-OH is synthesized by N-(9-Fluorenylmethoxycarbonyloxy)succinimide (Fmoc-ONSu) and 1-Methyl-Ltrypthophan and can be used for protein or peptide synthesis .
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- HY-153151
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Others
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Cancer
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Fmoc-DON-Boc (Compound 8b) is an Fmoc-protected compound that can be used for the synthesis of proagent of 6-diazo-5-oxo-L-norleucine (DON; HY-108357). DON is a glutamine antagonist .
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- HY-W009204S3
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- HY-W009204S2
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- HY-79131S
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- HY-Y0134S
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- HY-W011210
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Amino Acid Derivatives
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Others
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Fmoc-Pra-OH is a Glycine (HY-Y0966) derivative . Fmoc-Pra-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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- HY-W008371
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- HY-W141987
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- HY-W142030
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- HY-131833A
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ADC Linker
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Cancer
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Fmoc-Gly-Gly-D-Phe-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Gly-Gly-D-Phe-OH is the D-isomer of Fmoc-Gly-Gly-Phe-OH (HY-131833).
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- HY-131833G
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ADC Linker
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Cancer
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Fmoc-Gly-Gly-Phe-OH GMP is a GMP grade Fmoc-Gly-Gly-Phe-OH (HY-131833). Fmoc-Gly-Gly-Phe-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
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- HY-128929
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ADC Linker
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Cancer
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Fmoc-PEA (Example 1-2) is a used as a cleavable linker for antibody-drug conjugates (ADC) .
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- HY-112516
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Others
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Others
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Fmoc-Lys(amino aldehyde)-Boc is a lysine derivative, and is very sensitive to acid and heat. Fmoc-Lys(amino aldehyde)-Boc and can be used in solid phase synthesis .
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- HY-44234A
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ADC Linker
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Cancer
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Fmoc-Gly-Gly-D-Phe-OtBu is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Gly-Gly-D-Phe-OtBu is the R-isomer of Fmoc-Gly-Gly-Phe-OtBu (HY-44234) .
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- HY-140945
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PROTAC Linkers
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Cancer
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Fmoc-Lys (biotin-PEG12)-OH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-W041983
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- HY-W011342
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- HY-W010839
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- HY-W041984
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- HY-W009006
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- HY-W009124
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- HY-134852
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- HY-137950
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- HY-W097163
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- HY-22296
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- HY-W010721
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- HY-W010782
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- HY-W141946
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- HY-W005815
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- HY-W141985
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- HY-W025807
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- HY-W007108
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- HY-W007706
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- HY-W007941
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- HY-W008016
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- HY-W008072
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- HY-W008869
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- HY-W008872
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- HY-W008958
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- HY-W008986
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- HY-W008926
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- HY-W008273
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- HY-W008256
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- HY-W008075
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- HY-W010962
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- HY-W010964
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- HY-W010965
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- HY-W011026
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- HY-W011089
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- HY-W013118
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- HY-W013143
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- HY-W013145
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- HY-W013185
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- HY-W011126
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- HY-W013659
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- HY-W010976
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- HY-W041990
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- HY-W040024
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- HY-W007942
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- HY-W002436
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- HY-W010943
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- HY-W010862
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- HY-W010830
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- HY-W010794
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- HY-W010734
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- HY-W009119
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- HY-W007798
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- HY-W142115
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- HY-W008021
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- HY-79125
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ADC Linker
PROTAC Linkers
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Cancer
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Fmoc-Hyp(Bom)-OH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Hyp(Bom)-OH is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs<
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- HY-101064S2
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N-FMoc-leucine-d3; NPC 15199-d3; NSC 334290-d3
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PPAR
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Fmoc-leucine-d3 is the deuterium labeled Fmoc-leucine. Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity in normal, diet-induced glucose-intolerant, and in diabetic db/db mice. Fmoc-leucine has a lower adipogenic activity[1].
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- HY-151695
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N2-FMoc-N6-[(propargyloxy)carbonyl]-L-lysine
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ADC Linker
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Others
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Fmoc-L-Lys(Pryoc)-OH (N2-Fmoc-N6-[(propargyloxy)carbonyl]-L-lysine) is a click chemistry reagent containing an azide group .
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- HY-W111226
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Amyloid-β
Amino Acid Derivatives
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Cardiovascular Disease
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Fmoc-His(3-Me)OH derives Histidine-associating compounds with biological activity. Fmoc-His(3-Me)OH, with Fmoc-citrulline-OH, Fmoc-His(1-Me)-OH together, forms tri-peptides and shows vasodilating effect with EC50s of 2.7-4.7 mM in 1.0 mM Phenylephrine (PE)-contracted aorta rings. Fmoc-His(3-Me)OH (resin) also makes Methyl-His-Gly-Lys (His(3-Me)-Gly-Lys), thus acts as an [Ca 2+]i inhibitor. Fmoc-His(3-Me)OH methylates NAHIS02, making it unable to block the Alzheimer's Aβ channel .
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- HY-I1111S3
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- HY-130477
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PROTAC Linkers
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Cancer
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Fmoc-Lys (biotin-PEG4)-OH is a biotin-labeled, PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-79128S
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- HY-Y1169
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4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate; FMoc-L-Asp(OtBu)-OH
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Fmoc-Asp(OtBu)-OH (4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate) is a aspartate derivative containing amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for peptide synthesis .
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- HY-W008689
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N-FMoc-6-Aminohexanoic acid
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Biochemical Assay Reagents
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Others
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Fmoc-ε-Acp-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-151780
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ADC Linker
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Others
|
Fmoc-L-Dap(Pentynoyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Dap(Pentynoyl)-OH serves as an amino acid building block for introducing alkyne functions into peptide sequences by standard Fmoc/tBu protocols. The alkyne residue can be engaged for copper catalyzed click reaction with organic azides or with tetrazines for copper-free conjugations . Fmoc-L-Dap(Pentynoyl)-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
|
-
- HY-W011277
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-azetidine-3-carboxylic acid is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-azetidine-3-carboxylic acid is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-126532
-
|
Drug-Linker Conjugates for ADC
|
Cancer
|
Fmoc-Val-Cit-PAB-Duocarmycin TM is a agent-linker conjugate for ADC by using the antitumor antibiotic, Duocarmycin TM, linked via Fmoc-Val-Cit-PAB.
|
-
- HY-W141961
-
-
- HY-147104
-
|
Fluorescent Dye
|
Others
|
Fmoc-Lys(5-FITC)-OH is a marker for polypeptides or proteins. FITC is a fluorescence probe for the labeling of amines. FITC is a pH- and Cu 2+-sensitive fluorescence dye .
|
-
- HY-133404
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-aminooxy-PFP ester is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-I1112
-
-
- HY-W041992
-
-
- HY-W041987
-
-
- HY-W141986
-
-
- HY-W010732
-
-
- HY-W112057
-
-
- HY-W008395
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-D-Pra-OH is a Glycine (HY-Y0966) derivative . Fmoc-D-Pra-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
|
-
- HY-W039112
-
-
- HY-Y1250
-
FMoc glycine; N-(9-Fluorenylmethoxycarbonyl)glycine; N-Fluorenylmethoxycarbonylglycine; NPC 14692; NSC 334288; [[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]acetic acid
|
|
|
Fmoc-Gly-OH (Fmoc glycine) is a Fmoc-protected glycine derivative, can be used for the synthesis of compounds .
|
-
- HY-19821S1
-
FMoc-L-isoleucine-13C6,15N
|
Isotope-Labeled Compounds
|
Others
|
Fmoc-Ile-OH- 13C6, 15N is the 13C and 15N labeled Fmoc-Ile-OH[1]. Fmoc-Ile-OH is an isoleucine derivative[2].
|
-
- HY-Y1250S2
-
-
- HY-151778
-
|
ADC Linker
|
Others
|
Fmoc-Abg(N3)-OH is a click chemistry reagent containing an azide group. Fmoc-Abg(N3)-OH has the potential to synthesize peptide nucleic acids (PNA) and peptoids.
|
-
- HY-Y1169S1
-
|
Isotope-Labeled Compounds
|
Others
|
Fmoc-Asp(OtBu)-OH- 13C4, 15N is the 13C and 15N labeled Fmoc-Asp(OtBu)-OH[1]. Fmoc-Asp(OtBu)-OH (4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate) is a aspartate derivative containing amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for peptide synthesis[2].
|
-
- HY-66024
-
-
- HY-W010714
-
-
- HY-W010888
-
-
- HY-W010924
-
-
- HY-W008156
-
-
- HY-W041986
-
-
- HY-W008866
-
-
- HY-Y1844
-
|
|
|
Fmoc-D-Glu(OtBu)-OH is a glutamic acid derivative .
|
-
- HY-W043473
-
-
- HY-W008426
-
-
- HY-W013144
-
-
- HY-W041985
-
-
- HY-W022227
-
-
- HY-W010724
-
-
- HY-W010698
-
-
- HY-W140794
-
-
- HY-W008560
-
-
- HY-P3882
-
|
Amino Acid Derivatives
|
Neurological Disease
|
Fmoc-Ala-Glu-Gln-Lys-NH2 (AEQK) is a tetrapeptide. Fmoc-Ala-Glu-Gln-Lys-NH2 is the inactive control for Fmoc-Ala-Glu-Asn-Lys-NH2 (AENK) peptide inhibitor. AENK blocks proteolysis of UNC5C protein .
|
-
- HY-44980G
-
|
ADC Linker
|
Others
|
Fmoc-Gly-NH-CH2-acetyloxy GMP is a GMP grade Fmoc-Gly-NH-CH2-acetyloxy (HY-44980). Fmoc-Gly-NH-CH2-acetyloxy is a cleavable linker that can be used to synthesize antiboy-drug Conjugates (ADCs).
|
-
- HY-W008555
-
-
- HY-W008922
-
-
- HY-W010997
-
-
- HY-101064S
-
|
PPAR
|
Others
|
Fmoc-leucine- 13C is a 13C-labeled Boc-Glycine[1].
|
-
- HY-139292
-
|
Amino Acid Derivatives
|
Cancer
|
Fmoc-NH-PEG6-alcohol is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG6-alcohol is extracted from patent WO2016030791, example comp 91 .
|
-
- HY-19318
-
|
ADC Linker
|
Cancer
|
Fmoc-Val-Cit-PAB is a cleavable antibody-conjugated active molecule (ADC) commonly used linker.
|
-
- HY-151660
-
|
ADC Linker
|
Others
|
Fmoc-D-Lys(N3)-OH is a click chemistry reagent containing an azide group. Fmoc-D-Lys(N3)-OH can be used for the research of various biochemical .
|
-
- HY-W010986
-
-
- HY-79131S3
-
-
- HY-W008999
-
-
- HY-W009023
-
-
- HY-W016031
-
-
- HY-W010825
-
-
- HY-W010894
-
-
- HY-W008527
-
-
- HY-W008995
-
-
- HY-W008971
-
-
- HY-W013714
-
-
- HY-W010931
-
-
- HY-W010871
-
-
- HY-W010836
-
-
- HY-W010811
-
-
- HY-66026
-
-
- HY-66025
-
-
- HY-W013735
-
-
- HY-Y1250S1
-
-
- HY-153976
-
|
Drug-Linker Conjugates for ADC
|
Cancer
|
Fmoc-Gly3-VC-PAB-MMAE is a Drug-Linker Conjugates for ADC. Fmoc-Gly3-VC-PAB-MMAE consists of Monomethyl auristatin E (HY-15162) and a linker .
|
-
- HY-W009204S1
-
-
- HY-79131S1
-
-
- HY-W008371S1
-
-
- HY-W009204S4
-
-
- HY-135418
-
|
ADC Linker
|
Cancer
|
Fmoc-Asp-NH2 is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
|
-
- HY-W023121
-
|
ADC Linker
|
Cancer
|
Fmoc-Gly-Gly-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-W097109A
-
|
ADC Linker
|
Cancer
|
Fmoc-(D-Phe)-Osu is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-P5299
-
-
- HY-156813
-
|
ADC Linker
|
Cancer
|
Fmoc-Val-Ala-aminomethyl acetate (Compound 58b) is an ADC Linker, and can be used for synthesis of ADCs .
|
-
- HY-151687
-
|
ADC Linker
|
Others
|
Fmoc-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Tyr(2-azidoethyl)-OH is unnatural Fmoc-protected Tyrosine derivative bears an azidoethyl substitution as reactive handle e.g. for biorthogonal conjugations, via a Cu(I)-catalyzed 1,3-dipolar Click cycloaddition with alkynes. And azido-UAAs can be employed as IR reporters .
|
-
- HY-W022281
-
-
- HY-W008529
-
-
- HY-W013740
-
-
- HY-W013745
-
-
- HY-W010770
-
-
- HY-W013769
-
-
- HY-W013749
-
-
- HY-46859
-
-
- HY-122456
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-122459
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG5-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-126882
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG6-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140461
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG10-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140440
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-aminooxy-PEG4-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W040245
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-amino-PEG5-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140441
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-aminooxy-PEG12-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-141102
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG24-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-141101
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG12-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-130907
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-PEG24-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-138330
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG5-NHBoc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-138434
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG14-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-138720
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG9-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-138721
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG10-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W143484
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG3-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-19318A
-
|
ADC Linker
|
Cancer
|
Fmoc-D-Val-Cit-PAB is a cleavable linker for antibody-agent-conjugation (ADC) .
|
-
- HY-19318B
-
|
ADC Linker
|
Cancer
|
Fmoc-D-Val-Cit-PAB is a cleavable linker for antibody-agent-conjugation (ADC) .
|
-
- HY-W013779
-
-
- HY-W045822
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-Lys(Pal-Glu-OtBu)-OH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-Lys(Pal-Glu-OtBu)-OH is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-140460
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG7-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140462
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG20-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140463
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG23-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140464
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG36-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W013081
-
|
Biochemical Assay Reagents
|
Others
|
Fmoc-Gln(Trt)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W010856
-
|
Biochemical Assay Reagents
|
Others
|
Fmoc-Orn(Boc)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W048700
-
-
- HY-151669
-
|
ADC Linker
|
Others
|
Fmoc-D-Aha-OH is a click chemistry reagent containing an azide . Fmoc-D-Aha-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-W010921S
-
-
- HY-104004
-
FMoc-Ser-(GalNAc(Ac)3-alpha-D)-OH; FMoc-Ser[GalNAc(Ac)3-α-D]-OH; FMoc-Ser(Ac3AcNH-α-Gal)-OH
|
Amino Acid Derivatives
|
Cancer
|
Fmoc-Ser(O-α-D-GalNAc(OAc)3)-OH is a agent for cancer.
|
-
- HY-129361
-
-
- HY-W008997
-
-
- HY-W010957
-
-
- HY-W142008
-
-
- HY-W008996
-
-
- HY-W008972
-
-
- HY-W010974
-
-
- HY-W141945
-
-
- HY-W010927
-
-
- HY-W010926
-
-
- HY-W010838
-
-
- HY-W017617
-
-
- HY-W016028
-
-
- HY-W142086
-
-
- HY-79129
-
|
ADC Linker
|
Cancer
|
Fmoc-D-Trp(Boc)-OH is a cleavable ADC linker that used in the synthesis of antibody-drug conjugates (ADCs).
|
-
- HY-W013780S2
-
-
- HY-W013726
-
-
- HY-P4198
-
-
- HY-400191
-
|
ADC Linker
|
Cancer
|
Fmoc-Gly-Gly-allyl propionate is a cleavable linker that can be used to synthesize Antibody-Drug Conjugates (ADCs).
|
-
- HY-160072
-
|
Others
|
Cancer
|
Fmoc-NH-PEG2-NHS ester is an intermediate used in the synthesis of E-selectin antagonists [1] .
|
-
- HY-W007941S
-
-
- HY-W101718
-
|
Isotope-Labeled Compounds
ADC Linker
|
Cancer
|
Fmoc-N-(2-Boc-aminoethyl)-Gly-OH is a Fmoc-protected glycine derivative that can be used in antibody agent coupling (ADC) synthesis. ADC consists of antibodies that are linked to ADC cytotoxins via ADC junctions[1].
|
-
- HY-104004A
-
FMoc-Ser-(GalNAc(Ac)3-beta-D)-OH; FMoc-Ser[GalNAc(Ac)3-β-D]-OH; FMoc-Ser(Ac3AcNH-β-Gal)-OH
|
Amino Acid Derivatives
|
Others
|
Fmoc-Ser(O-β-D-GalNAc(OAc)3)-OH is a serine derivative .
|
-
- HY-151842
-
|
ADC Linker
|
Others
|
Fmoc-EDA-N3 is a click chemistry reagent containing an azide group . Fmoc-EDA-N3 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-144628
-
|
ADC Linker
|
Cancer
|
Fmoc-Asn-Pro-Val-PABC-PNP (compound 6) is a potent ADC Linker .
|
-
- HY-44234
-
|
ADC Linker
|
Cancer
|
Fmoc-Gly-Gly-Phe-OtBu is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-140118
-
|
ADC Linker
|
Cancer
|
Fmoc-NH-ethyl-SS-propionic acid is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-126353
-
|
ADC Linker
|
Cancer
|
Fmoc-Val-Ala-PAB-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-136107
-
|
ADC Linker
|
Cancer
|
Fmoc-Phe-Lys(Trt)-PAB is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-136136
-
|
ADC Linker
|
Cancer
|
Fmoc-Val-Ala-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-131833
-
|
ADC Linker
|
Cancer
|
Fmoc-Gly-Gly-Phe-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-139353
-
|
ADC Linker
|
Cancer
|
Fmoc-Phe-Lys(Boc)-PAB is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-W540122
-
-
- HY-151663
-
FMoc-Abu(3-N3)-OH (2R,3R)
|
ADC Linker
|
Others
|
Fmoc-Abu(3-N3) (Fmoc-Abu(3-N3)-OH) (2R,3R) is a click chemistry reagent containing an azide group. Fmoc-Abu(3-N3) (2R,3R) can be used for the research of various biochemical .
|
-
- HY-141103
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NMe-PEG4-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-126880
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG8-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140442
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-aminooxy-PEG12-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-133470
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG4-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W008034
-
|
Biochemical Assay Reagents
|
Others
|
Fmoc-L-Trp(Boc)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-19318C
-
|
ADC Linker
|
Cancer
|
Fmoc-D-Val-D-Cit-PAB is a cleavable linker for antibody-agent-conjugation (ADC) .
|
-
- HY-W010982
-
-
- HY-P2396
-
-
- HY-P2400
-
-
- HY-P2405
-
-
- HY-P2390
-
-
- HY-P2393
-
-
- HY-P2398
-
-
- HY-P2409
-
-
- HY-P2410
-
-
- HY-P2386
-
-
- HY-P2385
-
-
- HY-156825
-
|
Others
|
Others
|
Fmoc-Ser-Ribose(diBoc)-5-phosphatediAllyl (compound 1) is used for protein modification .
|
-
- HY-W010850
-
-
- HY-114430
-
|
ADC Linker
|
Others
|
Fmoc-Phe-Lys(Boc)-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
|
-
- HY-141902S
-
-
- HY-P2402
-
-
- HY-129350
-
|
ADC Linker
|
Cancer
|
Fmoc-Phe-Lys(Trt)-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-140119
-
|
ADC Linker
|
Cancer
|
Fmoc-NH-ethyl-SS-propionic NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-130933
-
|
ADC Linker
|
Cancer
|
Fmoc-Ala-Ala-Asn(Trt)-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-130175
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG4-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG4-CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-130364
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG6-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG6-CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-133062
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG5-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG5-CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-133063
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG8-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG8-CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W055861
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG1-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG1-CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-151786
-
|
ADC Linker
|
Others
|
Fmoc-L-Lys(Pentynoyl-DIM)-OH is a click chemistry reagent containing an azide. Fmoc-L-Lys(Pentynoyl-DIM)-OH can be used as a SPPS building block for the “helping hand” strategy for purification of highly insoluble peptides. Solubilizing residues are attached to the Lys side-chains using Click-chemistry. The solubilizing tag can be removed with 1M hydrazine or hydroxylamine solution .
|
-
- HY-151671
-
|
ADC Linker
|
Others
|
Fmoc-L-MeLys(N3)-OH is a click chemistry reagent containing an azide. Fmoc-L-MeLys(N3)-OH is a SPPS building-block for the introduction of N-Me-Lys that can be modified at the N3-group using Click-chemistry . Fmoc-L-MeLys(N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-141464
-
FMoc-Asn(Ac3AcNH-beta-Glc)-OH
|
Amino Acid Derivatives
|
Cancer
|
Fmoc-L-Asn(beta-D-GlcNAc(Ac)3)-OH (Fmoc-Asn(Ac3AcNH-beta-Glc)-OH) can be used in the synthesis of silicon-fluoride acceptor (SiFA) derivatized octreotate derivatives. SiFA-octreotate analogues, as tumor imaging agents, are useful tool for the research of positron emission tomography (PET) .
|
-
- HY-W008867
-
-
- HY-W008908
-
-
- HY-W141821
-
-
- HY-134681
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG5-NH-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-134715
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG4-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-138320
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG36-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-138331
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG6-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W096094
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG2-alcohol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-44980
-
|
ADC Linker
|
Others
|
Fmoc-Gly-NH-CH2-acetyloxy is a cleavable linker that can be used to synthesize antiboy-drug Conjugates (ADCs).
|
-
- HY-43279
-
|
ADC Linker
|
Cancer
|
Fmoc-Gly-NH-CH2-O-CH2COOH is an ADC linker. Fmoc-Gly-NH-CH2-O-CH2COOH can be used for synthesis of ADCs .
|
-
- HY-P2389
-
-
- HY-P2395
-
-
- HY-P2397
-
-
- HY-P2399
-
-
- HY-P2401
-
-
- HY-P2403
-
-
- HY-P2404
-
-
- HY-P2407
-
-
- HY-P2408
-
-
- HY-P2384
-
-
- HY-P2388
-
-
- HY-P2411
-
-
- HY-P2391
-
-
- HY-P2412
-
-
- HY-P2387
-
-
- HY-136106
-
|
ADC Linker
|
Cancer
|
Fmoc-Gly3-Val-Cit-PAB is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-P2394
-
-
- HY-W000434
-
FMoc-15-amino-4,7,10,13-tetraoxapentadecanoic acid
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG4-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG4-CH2CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140013
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG1-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140465
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NMe-PEG4-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-131955
-
|
ADC Linker
|
Cancer
|
Fmoc-aminooxy-PEG2-NH2 is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-W007798S
-
-
- HY-46346
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-Gly-NH-CH2-O-CH2-Cbz is a PROTAC linker and a maleimide-GGFG peptide linker. Fmoc-Gly-NH-CH2-O-CH2-Cbz can be used in the synthesis of the Deruxtecan .
|
-
- HY-136154
-
|
ADC Linker
|
Cancer
|
Fmoc-Glu-(Boc)-Val-Cit-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-151826
-
|
ADC Linker
|
Others
|
Fmoc-D-Lys(pentynoyl)-OH is a click chemistry reagent containing an azide group. Used to introduce alkyne functionality into peptides that can be further modified using Click-chemistry .
|
-
- HY-151733
-
|
ADC Linker
|
Others
|
Fmoc-D-Dbu(N3)-OH is a click chemistry reagent containing an Azide . Fmoc-D-Dbu(N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-W749603
-
|
Biochemical Assay Reagents
|
Others
|
Fmoc-L-Lys-mono-amide-DOTA-tris(t-Bu ester)is a bifunctional chelator (Bifunctional Chelator; BFC) and a macrocyclic DOTA derivative used for tumor pre-targeting. Fmoc-L-Lys-mono-amide-DOTA-tris(t-Bu ester) can be used for conjugation of peptides and radionuclides.
|
-
- HY-W141817
-
-
- HY-I1111S1
-
-
- HY-132099
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG2-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Fmoc-N-amido-PEG2-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-132110
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG3-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Fmoc-N-amido-PEG3-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-132111
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG5-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Fmoc-N-amido-PEG5-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-P3497
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-Cys-Asp10 is a non-releasable oligopeptide linker, involves in the synthesis of releasable oligopeptide linker. Releasable oligopeptide linker can be used to deliver agent to a bone fracture-homing oligopeptide and reduces fractured femur healing times .
|
-
- HY-120773
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG3-CH2CH2-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-126881
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG2-CH2CH2-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-79648S
-
|
Isotope-Labeled Compounds
|
Others
|
Fmoc-Methylalanine-d3 is the deuterium labeled Trifloxystrobin. Trifloxystrobin (CGA 279202) is a fungicide, with EC50s of 23.0 μg/L and 1.7 μg/L for Daphnia magna neonate and embryos, respectively, after treatment for 48 h[1].
|
-
- HY-W008568
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-amino-PEG3-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-135029
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-PEG3-CH2-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140466
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG11-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140467
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG12-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-141149
-
|
ADC Linker
|
Cancer
|
Fmoc-PEG4-Ala-Ala-Asn-PAB is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-130941
-
|
ADC Linker
|
Cancer
|
Fmoc-N-bis-PEG3-NH-Boc is a cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-136108
-
|
ADC Linker
|
Cancer
|
Fmoc-Gly3-Val-Cit-PAB-PNP is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-151781
-
|
ADC Linker
|
Others
|
Fmoc-L-Dap(Poc)-OH is a click chemistry reagent containing an azide group. Amino acid building block suitable for side chain Click conjugation with standard protocols and together with tetrazine linkers in copper-free Click conjugation (Diels-Alder) .
|
-
- HY-132988
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-Tyr(3-F,tBu)-OH is a cyclic peptide compound with high membrane permeability and can specifically binds to a target molecule (extracted from patent WO2018225864A1) .
|
-
- HY-160714
-
|
ADC Linker
|
Cancer
|
Fmoc-Ala-Ala-Ala-amide-C-O-C-COOH (Compound IM-3) is a cleavable ADC linker .
|
-
- HY-140340
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-pentanoic acid-NHS-SO3Na is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140668
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG-CH2COOH (MW 3400) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-140669
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-N-amido-PEG-CH2COOH (MW 5000) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W040231
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG3-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG3-CH2CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W040238
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG2-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG2-CH2CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-130167
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG9-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-NH-PEG9-CH2CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-45669
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-Gly-Gly-Phe-Gly-CH2-O-CH2-Cbz is a PROTAC linker and a maleimide-GGFG peptide linker. Fmoc-Gly-Gly-Phe-Gly-CH2-O-CH2-Cbz can be used in the synthesis of the Deruxtecan .
|
-
- HY-P3497A
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-Cys-Asp10 (TFA) is a non-releasable oligopeptide linker, involves in the synthesis of releasable oligopeptide linker. Releasable oligopeptide linker can be used to deliver agent to a bone fracture-homing oligopeptide and reduces fractured femur healing times .
|
-
- HY-151659
-
|
ADC Linker
|
Others
|
Fmoc-L-Lys(N3-Gly)-OH is a click chemistry reagent containing a lysine-containing azidoacetyl group building-block for SPPS and can be used for various biochemical studies .
|
-
- HY-W013780S
-
|
Isotope-Labeled Compounds
Autophagy
Bacterial
Antibiotic
|
Infection
|
Fmoc-Pro-OH-1- 13C is a 13C-labeled Sulfabenzamide. Sulfabenzamide (N-Sulfanilylbenzamide) is an antimicrobial agent and usually consumed in combination with Sulfathiazole and Sulfacetamide. Sulfabenzamide is effective against Gram-positive and negative ba
|
-
- HY-133471
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG3-C2-NH2 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-134682
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG5-C2-NH2 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-130077
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-PEG1-CH2CH2-NHS ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-141151
-
|
ADC Linker
|
Cancer
|
Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB is a cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-151679
-
|
ADC Linker
|
Others
|
Fmoc-L-Lys(4-N3-Z)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Lys(4-N3-Z)-OH acts as Lysine building-block for SPPS containing an Azide moiety as a bioorthogonal ligation handle, an infrared probe and a photo-affinity reagent. It can be decaged by trans-cyclooctenols via a strain-promoted 1,3-dipolar cycloaddition . Fmoc-L-Lys(4-N3-Z)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-I1111S4
-
|
Isotope-Labeled Compounds
|
Others
|
Fmoc-L-Val-OH- 15N is a 15N-labeled Leucomalachite green. Leucomalachite green is a triphenylmethane dye used to detect blood. Leucomalachite green, a major metabolite of malachite green, is a potential carcinogen, teratogen and mutagen[1][2].
|
-
- HY-W035378
-
|
ADC Linker
PROTAC Linkers
|
Cancer
|
Fmoc-N-methyl-PEG3-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Fmoc-N-methyl-PEG3-CH2CH2COOH is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-49453
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-Gly-Gly-(D-Phe)-Gly-CH2-O-CH2-Cbz is a PROTAC linker and a maleimide-GGFG peptide linker. Fmoc-Gly-Gly-(D-Phe)-Gly-CH2-O-CH2-Cbz can be used in the synthesis of the Deruxtecan .
|
-
- HY-22062
-
-
- HY-101064S4
-
-
- HY-W007706S
-
-
- HY-W145646
-
|
Biochemical Assay Reagents
|
Others
|
Fmoc-L-Ser((Ac)4-β-D-Glc)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-Y1250S4
-
|
Fungal
|
Infection
Cancer
|
Fmoc-Gly-OH-1- 13C is a 13C-labeled Carbendazim. Carbendazim is a potent and orally active broad-spectrum benzimidazole fungicide and can be acts as a pesticide for fungal diseases research, such as Seproria, Fusarium and Sclerotina[1][3]. Carbendazim is a
|
-
- HY-136155
-
|
ADC Linker
|
Cancer
|
Fmoc-NH-Azide-PEG4-L-Lysine-PFP ester is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Fmoc-NH-Azide-PEG4-L-Lysine-PFP ester is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-79130
-
Benzeneacetic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (S)-; (S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]phenylethanoic acid; (S)-N-FMoc-α-phenylglycine; N-9-Fluorenylmethoxycarbonyl-L-phenylglycine
|
Amino Acid Derivatives
|
Others
|
Fmoc-(S)-phenylglycine is a Glycine (HY-Y0966) derivative .
|
-
- HY-135821
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG12-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-133361
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG15-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-130870
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG11-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-133362
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG16-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-133363
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG19-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-133364
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG25-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-133365
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG30-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-79128S1
-
-
- HY-151825
-
|
ADC Linker
|
Others
|
Fmoc-L-Phe(4-NH-Poc)-OH is a click chemistry reagent containing an azide group. Used as an orthogonally protected building block in solid-phase peptide synthesis. Poc-group can be further modified using Click-chemistry .
|
-
- HY-W040135
-
-
- HY-W040246
-
-
- HY-114174
-
|
Amyloid-β
|
Neurological Disease
|
Fmoc-Ala-Glu-Asn-Lys-NH2 is a selective asparagine endopeptidase (AEP) inhibitor peptide and suppresses amyloid precursor protein (APP) cleavage. AEP, a pH-controlled cysteine proteinase, is activated during ageing and mediates APP proteolytic processing .
|
-
- HY-160069
-
|
PROTAC Linkers
|
Others
|
Fmoc-Gly-Gly-Gly-NH-PEG4-C2-COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs
|
-
- HY-W096128
-
|
PROTAC Linkers
|
Cancer
|
Fmoc-NH-PEG3-amide-CH2OCH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
|
-
- HY-W008016S
-
-
- HY-W013780S1
-
|
Isotope-Labeled Compounds
Fungal
|
Infection
|
Fmoc-Pro-OH- 13C5, 15N is a 15N-labeled and 13C-labled Pyrimethanil. Pyrimethanil is an anilinopyrimidine and broad-spectrum contact fungicide for the control of Botrytis spp. on a wide variety of crops[1]. Pyrimethanil inhibits the biosynthesis of methioni
|
-
- HY-151738
-
|
ADC Linker
|
Others
|
Fmoc-Aeg(N3)-OH is a click chemistry reagent containing an Azide. Alkylating the Nitrogen of an amide bond results in peptoid structures, which leads to conformational restrains, like N-methylation and allows backbone derivatisation. Altering cytotoxicity, bacterial cell selectivity and receptor pharmacology through formation of peptoid derivatives have been published for Cilengitide, Piscidin 1, and MC3, MC4 and MC5 receptor agonist. This building block enables design of macrocycles through intermolecular crosslinking or backbone stabilization through intermolecular ring-closure. This compound is a potential building block for the construction of (customized) peptide nucleic acids (PNAs) and for peptoid synthesis . Fmoc-Aeg(N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-45545
-
|
Others
|
Others
|
Fmoc-gly-gly-ph-gly-nh-ch2-o-ch2cooh can be used to synthesize the ADC Linker, LND1067 .
|
-
- HY-I1111S2
-
-
- HY-156810
-
|
ADC Linker
|
Cancer
|
Fmoc-PEG4-GGFG-CH2-O-CH2-Cbz is a cleavable ADC linker containing 4 units of PEG, which can be used to synthesize active antibody conjugation molecules (ADC) .
|
-
- HY-49412
-
|
Others
|
Others
|
Fmoc-Gly-Gly-Phe-Gly-NH-CH2-O-CO-CH3 (compound DC-13-C) is an intermediate in the synthesis of Exatecan (HY-13631) derivatives .
|
-
- HY-151787
-
|
ADC Linker
|
Others
|
Fmoc-L-Lys(N3-Aca-DIM)-OH is a click chemistry reagent containing an azide group. Used as a SPPS building-block for the “helping hand” strategy for purification of highly insoluble peptides. Solubilizing residues are attached to the Lys side-chains using Click-chemistry. The solubilizing tag can be removed with 1M hydrazine or hydroxylamine solution .
|
-
- HY-W002327S
-
|
Isotope-Labeled Compounds
|
Others
|
Fmoc-Asn(Trt)-OH- 13C4, 15N2 is a 15N-labeled and 13C-labled 4-(4-(tert-Butyl)-2-ethoxyphenyl)-2-(2,6-difluorophenyl)-4,5-dihydrooxazole[1].
|
-
- HY-W250541
-
|
ADC Linker
|
Cancer
|
Fmoc-Gly-NH-CH2-O-Cyclopropane-CH2COOH is an intermediate in the synthesis of ADC linker.The linker composed of Benzyl 2-cyclopropyl-2-hydroxyacetate can be coupled to Exatecan (HY-13631) and combined with antibodies (such as antibody hu2F7) .
|
-
- HY-151829
-
|
ADC Linker
|
Others
|
Fmoc-L-Asn(EDA-N3)-OH is a click chemistry reagent containing an azide group. This building block is reported in literature for the modification of Amanitin via Click Chemistry. Alpha-Amanitin is the deadliest member of the amatoxin peptide family produced by the death-cap mushroom A. phalloides. It is an orally available, rigid, bicyclic octapeptide and one of the most lethal known natural products (LD50 = 50-100 μg/kg) acting as highly selective allosteric inhibitor of the RNA polymerase II .
|
-
- HY-49463
-
|
ADC Linker
|
Neurological Disease
|
Fmoc-Gly-Gly-Phe-Gly-CH2-O-CH2-Gly-CH2-O-CH2-Cbz is an ADC linker that can be used in the synthesis of ADCs (such as Trastuzumab deruxtecan and U3-1402).
|
-
- HY-79647
-
N-(FMoc-oxy)succinimide
|
Biochemical Assay Reagents
|
Others
|
N-(9-Fluorenylmethoxycarbonyloxy)succinimide is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-Y1250S6
-
FMoc glycine-13C2,15N; N-(9-Fluorenylmethoxycarbonyl)glycine-13C2,15N; N-Fluorenylmethoxycarbonylglycine-13C2,15N; NPC 14692-13C2-15N; NSC 334288-13C2,15N; [[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]acetic acid-13C2,15N
|
Isotope-Labeled Compounds
Influenza Virus
Bacterial
|
Infection
|
Fmoc-Gly-OH- 13C2, 15N is a 15N-labeled and 13C-labled Crystal Violet. Crystal violet (Basic Violet 3) is a triarylmethane dye. Crystal Violet (Gentian Violet) has antiviral effects against H1N1 and also has prominent bactericidal activities.
|
-
- HY-W010719
-
-
- HY-P0232
-
-
- HY-W048199
-
-
- HY-133472
-
|
PROTAC Linkers
|
Cancer
|
DBCO-NHCO-PEG3-Fmoc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . DBCO-NHCO-PEG3-Fmoc is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
|
-
- HY-150850S
-
-
- HY-W009049S
-
-
- HY-W116478S
-
-
- HY-151748
-
|
ADC Linker
|
Others
|
N3-L-Orn(Fmoc)-OH is a Fmoc-protected ornithine derivative, can be used as a click chemistry reagent.
|
-
- HY-W005144
-
-
- HY-W008196
-
-
- HY-Y1636S1
-
|
Isotope-Labeled Compounds
|
Others
|
L-Arginine-N-FMOC PBF-OH- 13C6 is the 13C labeled Fmoc-Arg(Pbf)-OH[1]. Fmoc-Arg(Pbf)-OH is an arginine derivative containing amine protecting group Fmoc. Fmoc-Arg(Pbf)-OH is a building block for the introduction of Arg into SPPS (Solid-Phase Peptide Synthesis)[2].
|
-
- HY-79132
-
-
- HY-78733
-
-
- HY-129362
-
|
ADC Linker
|
Cancer
|
Phe-Lys(Fmoc)-PAB is a cathepsin cleavable ADC linker used for the antibody-drug conjugates (ADCs) .
|
-
- HY-151715
-
|
ADC Linker
|
Others
|
N3-D-Dap(Fmoc)-OH is a click chemistry reagent. N3-D-Dap(Fmoc)-OH can be used as a component for coupling by click reaction and as an orthogonally protected diaminocarboxylic acid derivative .
|
-
- HY-P4277
-
|
Glyoxalase (GLO)
|
Others
|
N,S-Bis-Fmoc-Glutathione is a potent glyoxalase II inhibitor with a Ki value of 0.32 mM .
|
-
- HY-W006923
-
-
- HY-W002327S1
-
-
- HY-151681
-
cis-4-Azido-N-FMoc-D-proline
|
ADC Linker
|
Others
|
(2R,4R)-Fmoc-D-Pro(4-N3)-OH (cis-4-Azido-N-Fmoc-D-proline) is a click chemistry reagent containing an azide group .
|
-
- HY-W088097
-
-
- HY-138318
-
|
PROTAC Linkers
|
Cancer
|
DBCO-PEG3-amide-N-Fmoc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . DBCO-PEG3-amide-N-Fmoc is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
|
-
- HY-W036160
-
|
Amino Acid Derivatives
|
Others
|
N-Fmoc-O-ethyl-L-homoserine is an homoserine derivative, can be used in cyclic peptide compounds synthesis, as a reducing reagent .
|
-
- HY-W008575
-
|
Others
|
Others
|
N-Fmoc-N-methoxy-3-aminopropionic acid, a Weinreb amide linker, is a protein cross-linking agent .
|
-
- HY-W142171
-
-
- HY-W048205
-
|
Amino Acid Derivatives
|
Others
|
N6-Diazo-L-Fmoc-lysine is an active compand and can be used in a variety of chemical studies. N6-Diazo-L-Fmoc-lysine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-151843
-
|
ADC Linker
|
Others
|
N3-L-Lys(Fmoc)-OH is a click chemistry reagent containing an azide group . N3-L-Lys(Fmoc)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-140848
-
|
PROTAC Linkers
|
Cancer
|
Azide-PEG3-L-alanine-Fmoc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Azide-PEG3-L-alanine-Fmoc is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-W074914
-
-
- HY-152978
-
|
Nucleoside Antimetabolite/Analog
|
Others
|
2'-Deoxy-5'-O-DMT-N4-Fmoc-5-methylcytidine is a cytidine analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities .
|
-
- HY-151828
-
|
ADC Linker
|
Others
|
N3-Gly-Aeg(Fmoc)-OH is a click chemistry reagent containing an azide group. PNA building-block that can be further modified using Click-chemistry .
|
-
- HY-W142062
-
|
Amino Acid Derivatives
|
Others
|
cis-Fmoc-Pro(4-N3)-OH is a proline derivative . cis-Fmoc-Pro(4-N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-151749
-
|
ADC Linker
|
Others
|
N3-D-Lys(Fmoc)-OH is a click chemistry reagent containing an azide group. Click chemistry is a powerful chemical reaction with excellent bioorthogonality features: biocompatible, rapid and highly specific in biological environments . N3-D-Lys(Fmoc)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-W540023
-
|
ADC Linker
|
Cancer
|
Endo-BCN-Fmoc-L-Lysine is a linker containing the lyophilic bidentate macrocyclic ligand endo-BCN, which can further synthesize macrocyclic complexes. In click chemistry, endo-BCN can react with molecules containing azide groups to form stable triazoles in the absence of catalysts.
|
-
- HY-151689
-
|
ADC Linker
|
Others
|
(2S,3R)-Fmoc-Abu(3-N3)-OH is a click chemistry reagent containing an azide group. (2S,3R)-Fmoc-Abu(3-N3)-OH can be used for the research of various biochemical .
|
-
- HY-W039102
-
|
Amino Acid Derivatives
|
Cancer
|
N-Fmoc-N,O-dimethyl-L-serine is a serine derivative that can be used for coibamide A synthesis. Coibamide A is a marine natural product with potent antiproliferative activity against human cancer cells .
|
-
- HY-131082
-
|
ADC Linker
|
Cancer
|
(R)-8-Azido-2-(Fmoc-amino)octanoic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . (R)-8-Azido-2-(Fmoc-amino)octanoic acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-140846
-
|
PROTAC Linkers
|
Cancer
|
N-Fmoc-N'-(azido-PEG4)-L-Lysine is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs . N-Fmoc-N'-(azido-PEG4)-L-Lysine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-136058
-
|
ADC Linker
|
Cancer
|
N3-PEG4-amido-Lys(Fmoc)-acid is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . N3-PEG4-amido-Lys(Fmoc)-acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-151814
-
|
ADC Linker
|
Others
|
(2S,4S)-Fmoc-L-Pro(4-NHPoc)-OH is a click chemistry reagent containing an azide group.
|
-
- HY-152979
-
|
DNA/RNA Synthesis
|
Others
|
2'-Deoxy-5'-O-DMT-N4-Fmoc-5-methylcytidine 3'-CE-phosphoramidite is a cytidine analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities .
|
-
- HY-131087
-
|
ADC Linker
|
Cancer
|
Me-triacetyl-β-D-glucopyranuronate-Ph-CH2OH-Fmoc is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-140847
-
|
PROTAC Linkers
|
Cancer
|
N-Fmoc-N'-(azido-PEG4)-L-Lysine-PFP ester is an alkyl/ether and PEG-based PROTAC linker that can be used in the synthesis of PROTACs . N-Fmoc-N'-(azido-PEG4)-L-Lysine-PFP ester is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-151734
-
|
ADC Linker
|
Others
|
(2R,3S)-Fmoc-Abu(3-N3)-OH is a click chemistry reagent containing an azide group .
|
-
- HY-153195
-
|
Others
|
Cancer
|
Tetra-O-acetyl-β-D-galactopyranosyl-Ph-CH2OH-Fmoc can be used as conjugates to prepare antibody drug conjugates (ADCs) .
|
-
- HY-151762
-
|
ADC Linker
|
Others
|
(2R,4S)-Fmoc-D-Pro(4-N3)-OH is a click chemistry reagent containing an azide group.
|
-
- HY-151779
-
|
ADC Linker
|
Others
|
N3-L-Dab(Fmoc)-OH is a click chemistry reagent containing an azide group. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity .
|
-
- HY-152873
-
|
Nucleoside Antimetabolite/Analog
|
Others
|
Uridine-5-(N-Fmoc-methylamino)-acetyl (9-fluorenylmethyl) ester is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .
|
-
- HY-151850
-
|
ADC Linker
|
Others
|
(2S,4R)-Fmoc-L-Pro(4-N3)-OH is a click chemistry reagent containing an azide . (2S,4R)-Fmoc-L-Pro(4-N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
-
- HY-131296
-
|
Others
|
Inflammation/Immunology
|
5-A-RU-PABC-Val-Cit-Fmoc is the proagent of 5-A-RU . 5-A-RU, a precursor of bacterial Riboflavin, is a mucosal-associated invariant T (MAIT) cells activator. 5-A-RU forms potent MAIT-activating antigens via non-enzymatic reactions with small molecules, such as glyoxal and methylglyoxal, which are derived from other metabolic pathways .
|
-
- HY-153196
-
|
ADC Linker
|
Others
|
Tetra-O-acetyl-β-D-galactopyranosyl-Ph-CH2-(4-nitrophenyl)carbonate-Fmoc (Example 2.28.6) is an ADC linker that can be used to synthesize antibody-conjugated active molecules (ADCs) .
|
-
- HY-152983
-
|
DNA/RNA Synthesis
|
Others
|
2'-Deoxy-5'-O-DMT-N6-Fmoc-adenosine 3'CE-phosphoramidite is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277) .
|
-
- HY-129480
-
|
Others
|
Others
|
Vertilmicin sulfate combines with FMOC-Cl to form the Vertilmicin-FMOC-Cl adduct, and can be used for the determination of glucosamine sulfate in plasma .
|
-
- HY-D0300S1
-
-
- HY-W015339S
-
-
- HY-W134007S
-
-
- HY-W286743S
-
-
- HY-Z3421S
-
-
- HY-W321016S
-
-
- HY-W002071S
-
-
- HY-Y0869S
-
-
- HY-116285S
-
-
- HY-124547S
-
-
- HY-148463
-
|
ADC Linker
|
Cancer
|
MP-Ala-Ala-PAB is a cleavable ADC linker. Fmoc-Ala-Ala-PAB can be used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-148464
-
|
ADC Linker
|
Cancer
|
MC-Ala-Ala-PAB is a cleavable ADC linker. Fmoc-Ala-Ala-PAB can be used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-141833
-
|
Drug-Linker Conjugates for ADC
|
Cancer
|
Bi-Mc-VC-PAB-MMAE consists ADCs linker (Fmoc-Val-Cit-PAB) and potent tubulin inhibitor (MMAE). Bi-Mc-VC-PAB-MMAE is a agent-linker conjugate for ADC.
|
-
Cat. No. |
Product Name |
Type |
-
- HY-19318G
-
|
Fluorescent Dye
|
Fmoc-Val-Cit-PAB GMP is a GMP grade Fmoc-Val-Cit-PAB (HY-19318). Fmoc-Val-Cit-PAB is a cleavable antibody-conjugated active molecule (ADC) commonly used linker.
|
-
- HY-78921AG
-
|
Fluorescent Dye
|
Fmoc-3VVD-OH (GMP) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-131833G
-
|
Fluorescent Dye
|
Fmoc-Gly-Gly-Phe-OH GMP is a GMP grade Fmoc-Gly-Gly-Phe-OH (HY-131833). Fmoc-Gly-Gly-Phe-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-44980G
-
|
Fluorescent Dye
|
Fmoc-Gly-NH-CH2-acetyloxy GMP is a GMP grade Fmoc-Gly-NH-CH2-acetyloxy (HY-44980). Fmoc-Gly-NH-CH2-acetyloxy is a cleavable linker that can be used to synthesize antiboy-drug Conjugates (ADCs).
|
Cat. No. |
Product Name |
Type |
-
- HY-22295
-
|
Biochemical Assay Reagents
|
Fmoc-4-aminobutanoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W002327
-
|
Biochemical Assay Reagents
|
Fmoc-Asn(Trt)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Fmoc-Asn(Trt)-OH can be used for synthesis of Fmoc-based solid-phase peptide synthesis .
|
-
- HY-W008205
-
FMoc-L-Hydroxyproline
|
Biochemical Assay Reagents
|
Fmoc-Hyp-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-19318G
-
|
Biochemical Assay Reagents
|
Fmoc-Val-Cit-PAB GMP is a GMP grade Fmoc-Val-Cit-PAB (HY-19318). Fmoc-Val-Cit-PAB is a cleavable antibody-conjugated active molecule (ADC) commonly used linker.
|
-
- HY-78921AG
-
|
Biochemical Assay Reagents
|
Fmoc-3VVD-OH (GMP) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-131833G
-
|
Biochemical Assay Reagents
|
Fmoc-Gly-Gly-Phe-OH GMP is a GMP grade Fmoc-Gly-Gly-Phe-OH (HY-131833). Fmoc-Gly-Gly-Phe-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) .
|
-
- HY-W008689
-
N-FMoc-6-Aminohexanoic acid
|
Biochemical Assay Reagents
|
Fmoc-ε-Acp-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-44980G
-
|
Biochemical Assay Reagents
|
Fmoc-Gly-NH-CH2-acetyloxy GMP is a GMP grade Fmoc-Gly-NH-CH2-acetyloxy (HY-44980). Fmoc-Gly-NH-CH2-acetyloxy is a cleavable linker that can be used to synthesize antiboy-drug Conjugates (ADCs).
|
-
- HY-W013081
-
|
Biochemical Assay Reagents
|
Fmoc-Gln(Trt)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W010856
-
|
Biochemical Assay Reagents
|
Fmoc-Orn(Boc)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W008034
-
|
Biochemical Assay Reagents
|
Fmoc-L-Trp(Boc)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W749603
-
|
Chelators
|
Fmoc-L-Lys-mono-amide-DOTA-tris(t-Bu ester)is a bifunctional chelator (Bifunctional Chelator; BFC) and a macrocyclic DOTA derivative used for tumor pre-targeting. Fmoc-L-Lys-mono-amide-DOTA-tris(t-Bu ester) can be used for conjugation of peptides and radionuclides.
|
-
- HY-W145646
-
|
Biochemical Assay Reagents
|
Fmoc-L-Ser((Ac)4-β-D-Glc)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-79647
-
N-(FMoc-oxy)succinimide
|
Biochemical Assay Reagents
|
N-(9-Fluorenylmethoxycarbonyloxy)succinimide is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
Cat. No. |
Product Name |
Target |
Research Area |
- HY-79131
-
- HY-W019028
-
- HY-22297
-
- HY-W009204
-
- HY-W009151
-
- HY-W013780
-
- HY-79128
-
FMoc-L-Lys(Boc)-OH; FMoc-Lys(Boc)-OH; N-α-(FMoc)-N-ε-(t-boc)-L-Lysine-OH
|
Amino Acid Derivatives
|
Others
|
Fmoc-L-Lys (Boc)-OH is a lysine derivative .
|
- HY-W011002
-
- HY-W010880
-
- HY-W016032
-
- HY-W048671
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-Thr(TBDMS)-OH is a Threonine derivative. Fmoc-Thr(TBDMS)-OH can be used for the preparation of sugar ligand-tethered functional nucleic acid conjugates for targeted research .
|
- HY-W011210
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-Pra-OH is a Glycine (HY-Y0966) derivative . Fmoc-Pra-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
|
- HY-W008371
-
- HY-W141987
-
- HY-W142030
-
- HY-W041983
-
- HY-W011342
-
- HY-W010839
-
- HY-W041984
-
- HY-W009006
-
- HY-W009124
-
- HY-134852
-
- HY-137950
-
- HY-W097163
-
- HY-22296
-
- HY-W010721
-
- HY-W010782
-
- HY-W141946
-
- HY-W005815
-
- HY-W141985
-
- HY-W025807
-
- HY-W007108
-
- HY-W007706
-
- HY-W007941
-
- HY-W008016
-
- HY-W008072
-
- HY-W008869
-
- HY-W008872
-
- HY-W008958
-
- HY-W008986
-
- HY-W008926
-
- HY-W008273
-
- HY-W008256
-
- HY-W008075
-
- HY-W010962
-
- HY-W010964
-
- HY-W010965
-
- HY-W011026
-
- HY-W011089
-
- HY-W013118
-
- HY-W013143
-
- HY-W013145
-
- HY-W013185
-
- HY-W011126
-
- HY-W013659
-
- HY-W010976
-
- HY-W041990
-
- HY-W040024
-
- HY-W007942
-
- HY-W002436
-
- HY-W010943
-
- HY-W010862
-
- HY-W010830
-
- HY-W010794
-
- HY-W010734
-
- HY-W009119
-
- HY-W007798
-
- HY-W142115
-
- HY-W008021
-
- HY-W111226
-
|
Amyloid-β
Amino Acid Derivatives
|
Cardiovascular Disease
|
Fmoc-His(3-Me)OH derives Histidine-associating compounds with biological activity. Fmoc-His(3-Me)OH, with Fmoc-citrulline-OH, Fmoc-His(1-Me)-OH together, forms tri-peptides and shows vasodilating effect with EC50s of 2.7-4.7 mM in 1.0 mM Phenylephrine (PE)-contracted aorta rings. Fmoc-His(3-Me)OH (resin) also makes Methyl-His-Gly-Lys (His(3-Me)-Gly-Lys), thus acts as an [Ca 2+]i inhibitor. Fmoc-His(3-Me)OH methylates NAHIS02, making it unable to block the Alzheimer's Aβ channel .
|
- HY-W141961
-
- HY-W041992
-
- HY-W041987
-
- HY-W141986
-
- HY-W010732
-
- HY-W112057
-
- HY-W008395
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-D-Pra-OH is a Glycine (HY-Y0966) derivative . Fmoc-D-Pra-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
|
- HY-W039112
-
- HY-66024
-
- HY-W010714
-
- HY-W010888
-
- HY-W010924
-
- HY-W008156
-
- HY-W041986
-
- HY-W008866
-
- HY-W043473
-
- HY-W008426
-
- HY-W013144
-
- HY-W041985
-
- HY-W022227
-
- HY-W010724
-
- HY-W010698
-
- HY-W140794
-
- HY-W008560
-
- HY-P3882
-
|
Amino Acid Derivatives
|
Neurological Disease
|
Fmoc-Ala-Glu-Gln-Lys-NH2 (AEQK) is a tetrapeptide. Fmoc-Ala-Glu-Gln-Lys-NH2 is the inactive control for Fmoc-Ala-Glu-Asn-Lys-NH2 (AENK) peptide inhibitor. AENK blocks proteolysis of UNC5C protein .
|
- HY-W008922
-
- HY-W010997
-
- HY-W008999
-
- HY-W009023
-
- HY-W016031
-
- HY-W010825
-
- HY-W010894
-
- HY-W008527
-
- HY-W008995
-
- HY-W008971
-
- HY-W013714
-
- HY-W010931
-
- HY-W010871
-
- HY-W010836
-
- HY-W010811
-
- HY-66026
-
- HY-66025
-
- HY-W013735
-
- HY-P5299
-
- HY-W022281
-
- HY-W008529
-
- HY-W013740
-
- HY-W013745
-
- HY-W010770
-
- HY-W013769
-
- HY-W013749
-
- HY-W013779
-
- HY-W048700
-
- HY-W008997
-
- HY-W010957
-
- HY-W142008
-
- HY-W008996
-
- HY-W008972
-
- HY-W010974
-
- HY-W141945
-
- HY-W010927
-
- HY-W010926
-
- HY-W010838
-
- HY-W017617
-
- HY-W016028
-
- HY-W142086
-
- HY-W013726
-
- HY-P4198
-
- HY-104004A
-
FMoc-Ser-(GalNAc(Ac)3-beta-D)-OH; FMoc-Ser[GalNAc(Ac)3-β-D]-OH; FMoc-Ser(Ac3AcNH-β-Gal)-OH
|
Amino Acid Derivatives
|
Others
|
Fmoc-Ser(O-β-D-GalNAc(OAc)3)-OH is a serine derivative .
|
- HY-W010982
-
- HY-P2396
-
- HY-P2400
-
- HY-P2405
-
- HY-P2390
-
- HY-P2393
-
- HY-P2398
-
- HY-P2409
-
- HY-P2410
-
- HY-P2386
-
- HY-P2385
-
- HY-W010850
-
- HY-P2402
-
- HY-W008867
-
- HY-W008908
-
- HY-W141821
-
- HY-P2389
-
- HY-P2395
-
- HY-P2397
-
- HY-P2399
-
- HY-P2401
-
- HY-P2403
-
- HY-P2404
-
- HY-P2407
-
- HY-P2408
-
- HY-P2384
-
- HY-P2388
-
- HY-P2411
-
- HY-P2391
-
- HY-P2412
-
- HY-P2387
-
- HY-P2394
-
- HY-W141817
-
- HY-P3497
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-Cys-Asp10 is a non-releasable oligopeptide linker, involves in the synthesis of releasable oligopeptide linker. Releasable oligopeptide linker can be used to deliver agent to a bone fracture-homing oligopeptide and reduces fractured femur healing times .
|
- HY-P3497A
-
|
Amino Acid Derivatives
|
Others
|
Fmoc-Cys-Asp10 (TFA) is a non-releasable oligopeptide linker, involves in the synthesis of releasable oligopeptide linker. Releasable oligopeptide linker can be used to deliver agent to a bone fracture-homing oligopeptide and reduces fractured femur healing times .
|
- HY-22062
-
- HY-79130
-
Benzeneacetic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (S)-; (S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]phenylethanoic acid; (S)-N-FMoc-α-phenylglycine; N-9-Fluorenylmethoxycarbonyl-L-phenylglycine
|
Amino Acid Derivatives
|
Others
|
Fmoc-(S)-phenylglycine is a Glycine (HY-Y0966) derivative .
|
- HY-114174
-
|
Amyloid-β
|
Neurological Disease
|
Fmoc-Ala-Glu-Asn-Lys-NH2 is a selective asparagine endopeptidase (AEP) inhibitor peptide and suppresses amyloid precursor protein (APP) cleavage. AEP, a pH-controlled cysteine proteinase, is activated during ageing and mediates APP proteolytic processing .
|
- HY-W072732
-
FMoc-N(Bn)-L-Ala-OH
|
Peptides
|
Others
|
N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-benzyl-L-alanine is an alanine derivative .
|
- HY-W010719
-
- HY-P0232
-
- HY-23861
-
FMoc-N,N-dimethyl-L-Glutamine
|
Peptides
|
Others
|
N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N5,N5-dimethyl-L-glutamine is a glutamine derivative .
|
- HY-W048199
-
- HY-W005144
-
- HY-W008196
-
- HY-79132
-
- HY-78733
-
- HY-P4277
-
|
Glyoxalase (GLO)
|
Others
|
N,S-Bis-Fmoc-Glutathione is a potent glyoxalase II inhibitor with a Ki value of 0.32 mM .
|
- HY-W006923
-
- HY-W088097
-
- HY-W036160
-
|
Amino Acid Derivatives
|
Others
|
N-Fmoc-O-ethyl-L-homoserine is an homoserine derivative, can be used in cyclic peptide compounds synthesis, as a reducing reagent .
|
- HY-W142171
-
- HY-W048205
-
|
Amino Acid Derivatives
|
Others
|
N6-Diazo-L-Fmoc-lysine is an active compand and can be used in a variety of chemical studies. N6-Diazo-L-Fmoc-lysine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
- HY-W074914
-
- HY-W142062
-
|
Amino Acid Derivatives
|
Others
|
cis-Fmoc-Pro(4-N3)-OH is a proline derivative . cis-Fmoc-Pro(4-N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
|
- HY-W039102
-
|
Amino Acid Derivatives
|
Cancer
|
N-Fmoc-N,O-dimethyl-L-serine is a serine derivative that can be used for coibamide A synthesis. Coibamide A is a marine natural product with potent antiproliferative activity against human cancer cells .
|
Cat. No. |
Product Name |
Chemical Structure |
-
- HY-101064S3
-
|
Fmoc-leucine-d10 is the deuterium labeled Fmoc-leucine. Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity in normal, diet-induced glucose-intolerant, and in diabetic db/db mice. Fmoc-leucine has a lower adipogenic activity[1].
|
-
-
- HY-Y1250S5
-
|
Fmoc-Gly-OH- 13C2 is a 13C-labeled Fmoc-Gly-OH (HY-Y1250). Fmoc-Gly-OH (Fmoc glycine) is a Fmoc-protected glycine derivative, can be used for the synthesis of compounds .
|
-
-
- HY-19821S
-
|
Fmoc-Ile-OH- 15N is the 15N labeled Fmoc-Ile-OH[1].
|
-
-
- HY-79131S5
-
|
Fmoc-Phe-OH- 13C is the 13C labeled Fmoc-Phe-OH[1]. Fmoc-Phe-OH is a phenylalanine derivative[2].
|
-
-
- HY-W009204S5
-
|
Fmoc-Ala-OH- 13C3 is a 13C-labeled Fmoc-leucine. Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity in normal, diet-ind
|
-
-
- HY-79131S4
-
|
Fmoc-Phe-OH-d8 is the deuterium labeled Fmoc-Phe-OH.
|
-
-
- HY-W007720S
-
|
Fmoc-Ser-OH-d3 is the deuterium labeled Fmoc-Ser-OH.
|
-
-
- HY-W007720S1
-
|
Fmoc-Ser-OH- 15N is the 15N labeled Fmoc-Ser-OH.
|
-
-
- HY-W008371S2
-
|
Fmoc-Met-OH-d3 is the deuterium labeled Fmoc-Met-OH.
|
-
-
- HY-W009204S8
-
|
Fmoc-Ala-OH-d is the deuterium labeled Fmoc-Ala-OH[1].
|
-
-
- HY-W013780S3
-
|
Fmoc-Pro-OH-d3 is the deuterium labeled Fmoc-Pro-OH.
|
-
-
- HY-W052227S
-
|
Fmoc-DL-Ala-OH-d is the deuterium labeled DL-Alanine-2-N-fmoc.
|
-
-
- HY-I1111S
-
|
Fmoc-L-Val-OH-d8 is a deuterium labeled Fmoc-L-Val-OH. Fmoc-L-Val-OH is a kind of protect amino acids[1].
|
-
-
- HY-W009204S
-
|
Fmoc-Ala-OH- 15N is the 15N labeled Fmoc-Ala-OH[1].
|
-
-
- HY-W008371S
-
|
Fmoc-Met-OH- 15N is the 15N labeled Fmoc-Met-OH[1].
|
-
-
- HY-Y1250S
-
|
Fmoc-Gly-OH- 15N is the 15N labeled Fmoc-Gly-OH[1].
|
-
-
- HY-79131S2
-
|
Fmoc-Phe-OH-d5 is the deuterium labeled Fmoc-Phe-OH[1].
|
-
-
- HY-W009204S6
-
|
Fmoc-Ala-OH-d4 is the deuterium labeled Fmoc-Ala-OH[1].
|
-
-
- HY-Y1250S3
-
|
Fmoc-Gly-OH- 13C is a 13C-labeled Fmoc-Phe-OH[1].
|
-
-
- HY-W007941S1
-
|
Fmoc-Ser(tBu)-OH- 15N is the 15N labeled Fmoc-Ser(tBu)-OH[1]. Fmoc-Ser(tBu)-OH is a serine derivative[2].
|
-
-
- HY-101064S1
-
|
Fmoc-leucine- 13C6, 15N is a 15N-labeled and 13C-labled Fmoc-leucine. Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity
|
-
-
- HY-W007798S1
-
|
Fmoc-Cys(Trt)-OH-d2 is the deuterium labeled Fmoc-Cys(Trt)-OH. Fmoc-Cys(Trt)-OH is an N-terminal protected cysteine derivative[1].
|
-
-
- HY-W008072S
-
|
Fmoc-D-Ala-OH-d3 is the deuterium labeled Fmoc-D-Ala-OH.
|
-
-
- HY-W011026S
-
|
Fmoc-D-Phe-OH-d5 is the deuterium labeled Fmoc-D-Phe-OH.
|
-
-
- HY-W011026S1
-
|
Fmoc-D-Phe-OH-d8 is the deuterium labeled Fmoc-D-Phe-OH.
|
-
-
- HY-W010712S1
-
|
Fmoc-His(Trt)-OH- 15N3 is the 15N labeled Fmoc-His(Trt)-OH[1]. Fmoc-His(Trt)-OH has trityl (Trt) group to protect the side-chain of His. Fmoc-His(Trt)-OH has Fmoc group to protect -αNH2. Fmoc-His(Trt)-OH can be used for solid phase synthesis of peptides, providing protection against racemization and by-product formation[2].
|
-
-
- HY-W009204S3
-
|
Fmoc-Ala-OH-3- 13C is the 13C labeled Fmoc-Ala-OH[1].
|
-
-
- HY-W009204S2
-
|
Fmoc-Ala-OH-1- 13C is the 13C labeled Fmoc-Ala-OH[1].
|
-
-
- HY-79131S
-
|
Fmoc-Phe-OH- 13C6 is a 13C-labeled Fmoc-Ala-OH[1].
|
-
-
- HY-Y0134S
-
|
Fmoc-Glu(OtBu)-OH- 15N is a 15N-labeled Fmoc-L-Val-OH[1].
|
-
-
- HY-101064S2
-
|
Fmoc-leucine-d3 is the deuterium labeled Fmoc-leucine. Fmoc-leucine is a selective PPARγ modulator. Fmoc-leucine activates PPARγ with a lower potency but a similar maximal efficacy than rosiglitazone. Fmoc-leucine improves insulin sensitivity in normal, diet-induced glucose-intolerant, and in diabetic db/db mice. Fmoc-leucine has a lower adipogenic activity[1].
|
-
-
- HY-I1111S3
-
|
Fmoc-L-Val-OH- 13C5 is a 13C-labeled Fmoc-Gly-OH[1].
|
-
-
- HY-79128S
-
|
Fmoc-L-Lys (Boc)-OH- 15N2 is a 15N-labeled Fmoc-L-Lys (Boc)-OH (HY-79128). Fmoc-L-Lys (Boc)-OH is a lysine derivative .
|
-
-
- HY-19821S1
-
|
Fmoc-Ile-OH- 13C6, 15N is the 13C and 15N labeled Fmoc-Ile-OH[1]. Fmoc-Ile-OH is an isoleucine derivative[2].
|
-
-
- HY-Y1250S2
-
|
Fmoc-Gly-OH-2,2-d2 is the deuterium labeled Fmoc-Gly-OH-2,2[1].
|
-
-
- HY-Y1169S1
-
|
Fmoc-Asp(OtBu)-OH- 13C4, 15N is the 13C and 15N labeled Fmoc-Asp(OtBu)-OH[1]. Fmoc-Asp(OtBu)-OH (4-tert-Butyl N-(fluoren-9-ylmethoxycarbonyl)-L-aspartate) is a aspartate derivative containing amine protecting group Fmoc. Fmoc-Asp(OtBu)-OH can be used for peptide synthesis[2].
|
-
-
- HY-101064S
-
|
Fmoc-leucine- 13C is a 13C-labeled Boc-Glycine[1].
|
-
-
- HY-79131S3
-
|
Fmoc-Phe-OH- 15N is a 15N-labeled Propoxur.
|
-
-
- HY-Y1250S1
-
|
Fmoc-Gly-OH-2- 13C, 15N is the 13C, 15N labeled Fmoc-Gly-OH-2[1].
|
-
-
- HY-W009204S1
-
|
Fmoc-Ala-OH-3,3,3-d3 is the deuterium labeled Fmoc-Ala-OH-3,3,3[1].
|
-
-
- HY-79131S1
-
|
Fmoc-Phe-OH- 13C9, 15N is a 15N-labeled and 13C-labled Fmoc-Ala-OH[1].
|
-
-
- HY-W008371S1
-
|
Fmoc-Met-OH- 13C5, 15N is a 15N-labeled and 13C-labled Fmoc-L-Val-OH[1].
|
-
-
- HY-W009204S4
-
|
Fmoc-Ala-OH- 13C3, 15N is a 15N-labeled and 13C-labled Fmoc-Aib-OH[1].
|
-
-
- HY-W010921S
-
|
Fmoc-Trp-OH- 13C11, 15N2 is a 15N-labeled and 13C-labled Fmoc-Pro-OH[1].
|
-
-
- HY-W013780S2
-
|
Fmoc-Pro-OH- 15N is a 15N-labeled Glycine ethyl ester monohydrochloride[1].
|
-
-
- HY-W007941S
-
|
Fmoc-Ser(tBu)-OH- 13C3, 15N is a 15N-labeled and 13C-labled Fmoc-L-Lys (Boc)-OH[1].
|
-
-
- HY-141902S
-
|
FMOC-L-Glutamic Acid- 13C5, 15N-5-t-butyl ester is the 13C and 15N labeled FMOC-L-Glutamic Acid-5-t-butyl ester[1].
|
-
-
- HY-W007798S
-
|
Fmoc-Cys(Trt)-OH-1,2,3- 13C3, 15N is a 15N-labeled and 13C-labled Fmoc-Phe-OH[1].
|
-
-
- HY-I1111S1
-
|
Fmoc-L-Val-OH-1- 13C is a 13C-labeled Carbaryl. Carbaryl is used chiefly as an insecticide[1].
|
-
-
- HY-79648S
-
|
Fmoc-Methylalanine-d3 is the deuterium labeled Trifloxystrobin. Trifloxystrobin (CGA 279202) is a fungicide, with EC50s of 23.0 μg/L and 1.7 μg/L for Daphnia magna neonate and embryos, respectively, after treatment for 48 h[1].
|
-
- HY-W013780S
-
|
Fmoc-Pro-OH-1- 13C is a 13C-labeled Sulfabenzamide. Sulfabenzamide (N-Sulfanilylbenzamide) is an antimicrobial agent and usually consumed in combination with Sulfathiazole and Sulfacetamide. Sulfabenzamide is effective against Gram-positive and negative ba
|
-
- HY-I1111S4
-
|
Fmoc-L-Val-OH- 15N is a 15N-labeled Leucomalachite green. Leucomalachite green is a triphenylmethane dye used to detect blood. Leucomalachite green, a major metabolite of malachite green, is a potential carcinogen, teratogen and mutagen[1][2].
|
-
- HY-101064S4
-
|
Fmoc-leucine- 15N is a 15N-labeled and 13C-labled EIDD-1931. EIDD-1931 (Beta-d-N4-hydroxycytidine; NHC) is a novel nucleoside analog and behaves as a potent anti-virus agent. EIDD-1931 effectively inhibits the replication activity of venezuelan equine ence
|
-
- HY-W007706S
-
|
Fmoc-Thr(tBu)-OH- 13C4, 15N is a 15N-labeled and 13C-labled 2-Acetamidobenzamide[1].
|
-
- HY-Y1250S4
-
|
Fmoc-Gly-OH-1- 13C is a 13C-labeled Carbendazim. Carbendazim is a potent and orally active broad-spectrum benzimidazole fungicide and can be acts as a pesticide for fungal diseases research, such as Seproria, Fusarium and Sclerotina[1][3]. Carbendazim is a
|
-
- HY-79128S1
-
|
Fmoc-L-Lys (Boc)-OH- 13C6, 15N2 is a 15N-labeled and 13C-labled Triclabendazole.
|
-
- HY-W008016S
-
|
Fmoc-Tyr(tBu)-OH- 13C9, 15N is a 15N-labeled and 13C-labled Hypoxanthine. Hypoxanthine, a purine derivative, is a potential free radical generator and could be used as an indicator of hypoxia.
|
-
- HY-W013780S1
-
|
Fmoc-Pro-OH- 13C5, 15N is a 15N-labeled and 13C-labled Pyrimethanil. Pyrimethanil is an anilinopyrimidine and broad-spectrum contact fungicide for the control of Botrytis spp. on a wide variety of crops[1]. Pyrimethanil inhibits the biosynthesis of methioni
|
-
- HY-I1111S2
-
|
Fmoc-L-Val-OH- 13C5, 15N is a 15N-labeled and 13C-labled Pirimicarb. Pirimicarb is a fast-acting selective carbamate insecticide on a wide range of crops including cereals, sugar beet, potatoes, fruits and vegetables. Pirimicarb is an AChE inhibitor and an
|
-
- HY-W002327S
-
|
Fmoc-Asn(Trt)-OH- 13C4, 15N2 is a 15N-labeled and 13C-labled 4-(4-(tert-Butyl)-2-ethoxyphenyl)-2-(2,6-difluorophenyl)-4,5-dihydrooxazole[1].
|
-
- HY-Y1250S6
-
|
Fmoc-Gly-OH- 13C2, 15N is a 15N-labeled and 13C-labled Crystal Violet. Crystal violet (Basic Violet 3) is a triarylmethane dye. Crystal Violet (Gentian Violet) has antiviral effects against H1N1 and also has prominent bactericidal activities.
|
-
- HY-150850S
-
|
DL-Leucine-N-FMOC-d10 is the deuterium labeled DL-Leucine-N-FMOC[1].
|
-
- HY-W009049S
-
|
D-Methionine-N-fmoc-d3 is the deuterium labeled D-Methionine-N-fmoc.
|
-
- HY-W116478S
-
|
D-Leucine-N-fmoc-d10 is the deuterium labeled D-Leucine-N-fmoc.
|
-
- HY-Y1636S1
-
|
L-Arginine-N-FMOC PBF-OH- 13C6 is the 13C labeled Fmoc-Arg(Pbf)-OH[1]. Fmoc-Arg(Pbf)-OH is an arginine derivative containing amine protecting group Fmoc. Fmoc-Arg(Pbf)-OH is a building block for the introduction of Arg into SPPS (Solid-Phase Peptide Synthesis)[2].
|
-
- HY-W002327S1
-
|
L-Asparagine-N-Fmoc,N-beta-trityl- 15N2 is a 15N-labeled L-Asparagine-N-Fmoc,N-beta-trityl .
|
-
- HY-D0300S1
-
|
Leucomalachite green-d6 is the deuterium labeled Fmoc-Gly-OH[1].
|
-
- HY-W015339S
-
|
Octanoate- 13C (sodium) is a 13C-labeled Fmoc-Gly-OH[1].
|
-
- HY-W134007S
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Hexadecanoate- 13C (potassium) is a 13C-labeled Fmoc-L-Val-OH[1].
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- HY-W286743S
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CML-d4 is the deuterium labeled Fmoc-L-Lys (Boc)-OH[1].
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- HY-Z3421S
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Vonoprazan-d3 (fumarate) is the deuterium labeled Fmoc-Cys(Trt)-OH[1].
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- HY-W321016S
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SWEP-d3 is the deuterium labeled Fmoc-Tyr(tBu)-OH[1].
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- HY-W002071S
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2-Quinoxalinecarboxylic acid-d4 is the deuterium labeled Fmoc-Pro-OH[1].
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- HY-Y0869S
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4-Methoxybenzylamine-d3 is the deuterium labeled Fmoc-Ser(tBu)-OH[1].
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- HY-116285S
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n-Octyl β-D-glucopyranoside-d24 is the deuterium labeled Fmoc-L-Val-OH[1].
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- HY-124547S
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2,4-D methyl ester-d3 is the deuterium labeled Fmoc-Trp-OH[1].
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Cat. No. |
Product Name |
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Classification |
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- HY-W011210
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Alkynes
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Fmoc-Pra-OH is a Glycine (HY-Y0966) derivative . Fmoc-Pra-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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- HY-151640
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Azide
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Fmoc-DAP-N3 is a click chemistry reagent containing an azide group. Fmoc-DAP-N3 is a short, linear spacer molecule with Fmoc protected amino function. Fmoc-DAP-N3 can be used in click conjugation and amid bond formation either with small molecules or for bioconjugation with proteins and antibodies .
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- HY-151638
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Azide
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FMOC-3-azido-D-alanine is a click chemistry reagent containing an azide group .
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- HY-151637
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Alkynes
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Fmoc-N-propargyl-MPBA is a propargyl-substituted MPBA linker derived from 4-hydroxy-3-methoxybenzaldehyde. Fmoc-N-propargyl-MPBA can be elongated using standard Fmoc-based solid phase chemistry and linked to supports by standard coupling procedures . Fmoc-N-propargyl-MPBA is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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- HY-151695
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N2-FMoc-N6-[(propargyloxy)carbonyl]-L-lysine
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Alkynes
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Fmoc-L-Lys(Pryoc)-OH (N2-Fmoc-N6-[(propargyloxy)carbonyl]-L-lysine) is a click chemistry reagent containing an azide group .
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- HY-151780
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Alkynes
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Fmoc-L-Dap(Pentynoyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Dap(Pentynoyl)-OH serves as an amino acid building block for introducing alkyne functions into peptide sequences by standard Fmoc/tBu protocols. The alkyne residue can be engaged for copper catalyzed click reaction with organic azides or with tetrazines for copper-free conjugations . Fmoc-L-Dap(Pentynoyl)-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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- HY-W008395
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Alkynes
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Fmoc-D-Pra-OH is a Glycine (HY-Y0966) derivative . Fmoc-D-Pra-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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- HY-151778
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Azide
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Fmoc-Abg(N3)-OH is a click chemistry reagent containing an azide group. Fmoc-Abg(N3)-OH has the potential to synthesize peptide nucleic acids (PNA) and peptoids.
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- HY-151660
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Azide
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Fmoc-D-Lys(N3)-OH is a click chemistry reagent containing an azide group. Fmoc-D-Lys(N3)-OH can be used for the research of various biochemical .
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- HY-151687
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Azide
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Fmoc-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Tyr(2-azidoethyl)-OH is unnatural Fmoc-protected Tyrosine derivative bears an azidoethyl substitution as reactive handle e.g. for biorthogonal conjugations, via a Cu(I)-catalyzed 1,3-dipolar Click cycloaddition with alkynes. And azido-UAAs can be employed as IR reporters .
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- HY-151669
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Azide
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Fmoc-D-Aha-OH is a click chemistry reagent containing an azide . Fmoc-D-Aha-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151842
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Azide
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Fmoc-EDA-N3 is a click chemistry reagent containing an azide group . Fmoc-EDA-N3 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151663
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FMoc-Abu(3-N3)-OH (2R,3R)
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Azide
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Fmoc-Abu(3-N3) (Fmoc-Abu(3-N3)-OH) (2R,3R) is a click chemistry reagent containing an azide group. Fmoc-Abu(3-N3) (2R,3R) can be used for the research of various biochemical .
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- HY-151786
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Azide
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Fmoc-L-Lys(Pentynoyl-DIM)-OH is a click chemistry reagent containing an azide. Fmoc-L-Lys(Pentynoyl-DIM)-OH can be used as a SPPS building block for the “helping hand” strategy for purification of highly insoluble peptides. Solubilizing residues are attached to the Lys side-chains using Click-chemistry. The solubilizing tag can be removed with 1M hydrazine or hydroxylamine solution .
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- HY-151671
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Azide
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Fmoc-L-MeLys(N3)-OH is a click chemistry reagent containing an azide. Fmoc-L-MeLys(N3)-OH is a SPPS building-block for the introduction of N-Me-Lys that can be modified at the N3-group using Click-chemistry . Fmoc-L-MeLys(N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151826
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Alkynes
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Fmoc-D-Lys(pentynoyl)-OH is a click chemistry reagent containing an azide group. Used to introduce alkyne functionality into peptides that can be further modified using Click-chemistry .
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- HY-151733
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Azide
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Fmoc-D-Dbu(N3)-OH is a click chemistry reagent containing an Azide . Fmoc-D-Dbu(N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-132099
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Azide
PROTAC Synthesis
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Fmoc-N-amido-PEG2-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Fmoc-N-amido-PEG2-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-132110
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Azide
PROTAC Synthesis
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Fmoc-N-amido-PEG3-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Fmoc-N-amido-PEG3-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-132111
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Azide
PROTAC Synthesis
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Fmoc-N-amido-PEG5-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Fmoc-N-amido-PEG5-azide is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151781
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Alkynes
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Fmoc-L-Dap(Poc)-OH is a click chemistry reagent containing an azide group. Amino acid building block suitable for side chain Click conjugation with standard protocols and together with tetrazine linkers in copper-free Click conjugation (Diels-Alder) .
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- HY-151659
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Azide
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Fmoc-L-Lys(N3-Gly)-OH is a click chemistry reagent containing a lysine-containing azidoacetyl group building-block for SPPS and can be used for various biochemical studies .
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- HY-151679
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Azide
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Fmoc-L-Lys(4-N3-Z)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Lys(4-N3-Z)-OH acts as Lysine building-block for SPPS containing an Azide moiety as a bioorthogonal ligation handle, an infrared probe and a photo-affinity reagent. It can be decaged by trans-cyclooctenols via a strain-promoted 1,3-dipolar cycloaddition . Fmoc-L-Lys(4-N3-Z)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-136155
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ADC Synthesis
Azide
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Fmoc-NH-Azide-PEG4-L-Lysine-PFP ester is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . Fmoc-NH-Azide-PEG4-L-Lysine-PFP ester is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151825
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Alkynes
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Fmoc-L-Phe(4-NH-Poc)-OH is a click chemistry reagent containing an azide group. Used as an orthogonally protected building block in solid-phase peptide synthesis. Poc-group can be further modified using Click-chemistry .
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- HY-151738
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Azide
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Fmoc-Aeg(N3)-OH is a click chemistry reagent containing an Azide. Alkylating the Nitrogen of an amide bond results in peptoid structures, which leads to conformational restrains, like N-methylation and allows backbone derivatisation. Altering cytotoxicity, bacterial cell selectivity and receptor pharmacology through formation of peptoid derivatives have been published for Cilengitide, Piscidin 1, and MC3, MC4 and MC5 receptor agonist. This building block enables design of macrocycles through intermolecular crosslinking or backbone stabilization through intermolecular ring-closure. This compound is a potential building block for the construction of (customized) peptide nucleic acids (PNAs) and for peptoid synthesis . Fmoc-Aeg(N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151787
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Azide
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Fmoc-L-Lys(N3-Aca-DIM)-OH is a click chemistry reagent containing an azide group. Used as a SPPS building-block for the “helping hand” strategy for purification of highly insoluble peptides. Solubilizing residues are attached to the Lys side-chains using Click-chemistry. The solubilizing tag can be removed with 1M hydrazine or hydroxylamine solution .
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- HY-151829
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Azide
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Fmoc-L-Asn(EDA-N3)-OH is a click chemistry reagent containing an azide group. This building block is reported in literature for the modification of Amanitin via Click Chemistry. Alpha-Amanitin is the deadliest member of the amatoxin peptide family produced by the death-cap mushroom A. phalloides. It is an orally available, rigid, bicyclic octapeptide and one of the most lethal known natural products (LD50 = 50-100 μg/kg) acting as highly selective allosteric inhibitor of the RNA polymerase II .
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- HY-133472
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DBCO
PROTAC Synthesis
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DBCO-NHCO-PEG3-Fmoc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . DBCO-NHCO-PEG3-Fmoc is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
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- HY-151748
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Azide
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N3-L-Orn(Fmoc)-OH is a Fmoc-protected ornithine derivative, can be used as a click chemistry reagent.
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- HY-157052
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BCN
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exo-BCN-Fmoc-L-Lysine is a Click Amino Acid that can be used as a linker in the synthesis of PROTAC molecules. exo-BCN-Fmoc-L-Lysine contains a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
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- HY-151715
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Azide
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N3-D-Dap(Fmoc)-OH is a click chemistry reagent. N3-D-Dap(Fmoc)-OH can be used as a component for coupling by click reaction and as an orthogonally protected diaminocarboxylic acid derivative .
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- HY-151681
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cis-4-Azido-N-FMoc-D-proline
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Azide
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(2R,4R)-Fmoc-D-Pro(4-N3)-OH (cis-4-Azido-N-Fmoc-D-proline) is a click chemistry reagent containing an azide group .
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- HY-138318
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PROTAC Synthesis
DBCO
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DBCO-PEG3-amide-N-Fmoc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . DBCO-PEG3-amide-N-Fmoc is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
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- HY-W048205
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Azide
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N6-Diazo-L-Fmoc-lysine is an active compand and can be used in a variety of chemical studies. N6-Diazo-L-Fmoc-lysine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151843
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Azide
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N3-L-Lys(Fmoc)-OH is a click chemistry reagent containing an azide group . N3-L-Lys(Fmoc)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-140848
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Azide
PROTAC Synthesis
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Azide-PEG3-L-alanine-Fmoc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Azide-PEG3-L-alanine-Fmoc is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151828
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Azide
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N3-Gly-Aeg(Fmoc)-OH is a click chemistry reagent containing an azide group. PNA building-block that can be further modified using Click-chemistry .
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- HY-W142062
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Azide
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cis-Fmoc-Pro(4-N3)-OH is a proline derivative . cis-Fmoc-Pro(4-N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151749
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Azide
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N3-D-Lys(Fmoc)-OH is a click chemistry reagent containing an azide group. Click chemistry is a powerful chemical reaction with excellent bioorthogonality features: biocompatible, rapid and highly specific in biological environments . N3-D-Lys(Fmoc)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-W540023
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BCN
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Endo-BCN-Fmoc-L-Lysine is a linker containing the lyophilic bidentate macrocyclic ligand endo-BCN, which can further synthesize macrocyclic complexes. In click chemistry, endo-BCN can react with molecules containing azide groups to form stable triazoles in the absence of catalysts.
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- HY-151689
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Azide
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(2S,3R)-Fmoc-Abu(3-N3)-OH is a click chemistry reagent containing an azide group. (2S,3R)-Fmoc-Abu(3-N3)-OH can be used for the research of various biochemical .
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- HY-131082
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ADC Synthesis
Azide
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(R)-8-Azido-2-(Fmoc-amino)octanoic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . (R)-8-Azido-2-(Fmoc-amino)octanoic acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-140846
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Azide
PROTAC Synthesis
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N-Fmoc-N'-(azido-PEG4)-L-Lysine is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs . N-Fmoc-N'-(azido-PEG4)-L-Lysine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-136058
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Azide
ADC Synthesis
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N3-PEG4-amido-Lys(Fmoc)-acid is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) . N3-PEG4-amido-Lys(Fmoc)-acid is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151814
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Alkynes
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(2S,4S)-Fmoc-L-Pro(4-NHPoc)-OH is a click chemistry reagent containing an azide group.
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- HY-140847
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Azide
PROTAC Synthesis
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N-Fmoc-N'-(azido-PEG4)-L-Lysine-PFP ester is an alkyl/ether and PEG-based PROTAC linker that can be used in the synthesis of PROTACs . N-Fmoc-N'-(azido-PEG4)-L-Lysine-PFP ester is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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- HY-151734
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Azide
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(2R,3S)-Fmoc-Abu(3-N3)-OH is a click chemistry reagent containing an azide group .
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- HY-151762
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Azide
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(2R,4S)-Fmoc-D-Pro(4-N3)-OH is a click chemistry reagent containing an azide group.
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- HY-151779
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Azide
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N3-L-Dab(Fmoc)-OH is a click chemistry reagent containing an azide group. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity .
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- HY-151850
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Azide
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(2S,4R)-Fmoc-L-Pro(4-N3)-OH is a click chemistry reagent containing an azide . (2S,4R)-Fmoc-L-Pro(4-N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
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