Search Result
Results for "
CBZ
" in MedChemExpress (MCE) Product Catalog:
5
Biochemical Assay Reagents
7
Isotope-Labeled Compounds
| Cat. No. |
Product Name |
Target |
Research Areas |
Chemical Structure |
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- HY-B0246
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- HY-136626
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CBZ-Ala-Ala-Asn-AMC
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Fluorescent Dye
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Cancer
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Z-Ala-Ala-Asn-AMC (Cbz-Ala-Ala-Asn-AMC) is the legumain substrate. Overexpressed legumain in 293 HEK-Leg cells potently cleaved CBZ-Ala-Ala-Asn-AMC .
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- HY-129126
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NC9
1 Publications Verification
CBZ-Lys(Acr)-PEG2-dansyl
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Glutaminase
Microtubule/Tubulin
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Others
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NC9 (Cbz-Lys(Acr)-PEG2-dansyl) is an irreversible transglutaminase (TG) inhibitor. NC9 inhibits osteoblast differentiation and mineralization. NC9 destabilizes microtubules. NC9 can be used for the research of osteoblast differentiation .
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- HY-P1759
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Z-FR-AMC
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Cathepsin
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Others
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N-CBZ-Phe-Arg-AMC (Z-FR-AMC) is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
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- HY-B0246S
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- HY-147354
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LYTACs
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Cardiovascular Disease
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TriGalNAc CBz is a GalNAc derivative and tri-GalNAc is an asialoglycoprotein receptor (ASGPR) ligand. TriGalNAc CBz can be used for mRNA drug delivery as well as lysosomal targeted chimerism (LYTAC) studies .
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- HY-W016042
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Drug Intermediate
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Others
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N-Cbz-Hydroxy-L-proline is a chiral N-Cbz-protected amino acid derivative. N-Cbz-Hydroxy-L-proline is commonly used in the synthesis of polypeptides and pharmaceutical intermediates. N-Cbz-Hydroxy-L-proline undergoes decarboxylation under AlCl3/HFIP conditions .
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- HY-B0246R
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CBZ (Standard); NSC 169864 (Standard)
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Reference Standards
Sodium Channel
Autophagy
Mitophagy
Potassium Channel
Calcium Channel
HDAC
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Neurological Disease
Cancer
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Carbamazepine (Standard) is the analytical standard of Carbamazepine. This product is intended for research and analytical applications. Carbamazepine is an orally active pressure-sensitive sodium ion channel blocker with an IC50 of 131 μM. Carbamazepine blocks voltage gated Na +, Ca 2+, and K + channels, and is also a HDAC inhibitor (IC50: 2 μM). Carbamazepine is an anticonvulsant and can be used for research of epilepsy and neuropathic pain .
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- HY-P1759A
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Z-FR-AMC hydrochloride
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Cathepsin
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Others
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N-CBZ-Phe-Arg-AMC (Z-FR-AMC) hydrochloride is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
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- HY-B0246S2
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- HY-114267
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mTOR
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Others
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Cbz-B3A is a potent and selective inhibitor of mTORC1 signaling that appear to bind to ubiquilins 1, 2, and 4, and Cbz-B3A inhibits the phosphorylation of eIF4E-binding protein 1 (4EBP1).
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- HY-Y0588
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L-CBZ-Proline
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MMP
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Others
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Carbobenzoxyproline (L-Cbz-Proline) is an inhibitor of prolidase. Carbobenzoxyproline can be used for prolidase deficiency (PD) research .
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- HY-W095029
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Biochemical Assay Reagents
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Others
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Cbz-Gly-Pro-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-W011750
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- HY-45669
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PROTAC Linkers
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Cancer
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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 .
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- HY-W011197
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- HY-140488
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG3-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-B0246S3
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- HY-134113
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CBZ-Chromozym TH
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Biochemical Assay Reagents
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Others
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Z-Gly-Pro-Arg-pNA (z-GPR-pNA) is a photometric substrate in Prostate-Specific Antigen (PSA) activation protease assays. Z-Gly-Pro-Arg-pNA (z-GPR-pNA) can be used for the test of trypsin activity .
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- HY-177209
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Drug Intermediate
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Cancer
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Cbz-Val-(triAc-β-D-glucoside methyl ester)-Cbz is an intermediate used in the synthesis of ADC drug-linker .
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- HY-77475
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ADC Linker
PROTAC Linkers
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Cancer
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1-Cbz-3-Hydroxyazetidine is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). 1-Cbz-3-Hydroxyazetidine is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-78897
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- HY-P5027
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- HY-W009503
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- HY-46346
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PROTAC Linkers
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Cancer
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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 .
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- HY-W025724
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- HY-W004868
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ADC Linker
PROTAC Linkers
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Cancer
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1-Cbz-azetidine-3-carboxylic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). 1-Cbz-azetidine-3-carboxylic acid is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1]
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- HY-W336455
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PROTAC Linkers
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Cancer
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Cbz-PEG2-C2-NH2 is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-B0246S4
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CBZ-d4; NSC 169864-d4
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Isotope-Labeled Compounds
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Others
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Carbamazepine-d4 (CBZ-d4) is the deuterium labeled Carbamazepine (HY-B0246) . Carbamazepine is an orally active pressure-sensitive sodium ion channel blocker with an IC50 of 131 μM. Carbamazepine blocks voltage gated Na +, Ca 2+, and K + channels, and is also a HDAC inhibitor (IC50: 2 μM). Carbamazepine is an anticonvulsant and can be used for research of epilepsy and neuropathic pain.
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- HY-B0246S1
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- HY-160255
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CBZ-cysteine
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Beta-lactamase
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Infection
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N-Cbz-L-Cysteine (Cbz-cysteine) (compound 5) is a potent β-lactamase II inhibitor with a Ki value of 97 µM .
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- HY-W013905
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- HY-W294220
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PROTAC Linkers
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Cancer
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3-(Cbz-aminomethyl)azetidine (hydrochloride) is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-W009121
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- HY-76317
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N-CBZ-DL-proline; DL-CBZ-Proline
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Amino Acid Derivatives
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Others
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Z-DL-Pro-OH (N-Cbz-DL-proline) is a proline derivative, can be used for the synthesis of agents or other compounds .
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- HY-W009033
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- HY-W057967
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PROTAC Linkers
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Cancer
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Cbz-azaspiro[3.3]heptane-OH is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-133358
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG12-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-130192
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG8-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140487
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG2-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140489
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG5-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135925
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG1-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135923
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG2-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135913
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG3-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135926
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG1-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-P10198
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- HY-W103577
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CBZ-cycloleucine
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Biochemical Assay Reagents
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Others
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1-(Cbz-amino)cyclopentanecarboxylic acid (Cbz-cycloleucine) 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-160255A
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CBZ-D-Cys
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Beta-lactamase
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Infection
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N-Cbz-D-Cysteine (Cbz-D-Cys) (compound 5) is a potent β-lactamase II inhibitor with a Ki value of 20.1 µM .
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- HY-I1061
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- HY-126375R
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Benzyloxycarbonyl valacyclovir (Standard)
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Drug Intermediate
Reference Standards
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Infection
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Cbz-Valaciclovir (Standard) is the analytical standard of Cbz-Valaciclovir. This product is intended for research and analytical applications. Cbz-Valaciclovir (Benzyloxycarbonyl valacyclovir) can be used to prepare Valaciclovir (HY-17425) and for antiviral research .
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- HY-W1119953
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- HY-150242A
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Liposome
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Others
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Cbz-Ala-Ala-Asn TFA is a peptide that designed based on the sequence of the substrate of legumain. Legumain is a cysteine protease. Cbz-Ala-Ala-Asn TFA can be applied as a scaffold for drug delivery .
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- HY-400312
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- HY-W825985
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- HY-172292
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Biochemical Assay Reagents
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Others
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Cbz-GGFG-Bn 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-W574465
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- HY-W807367
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- HY-W402032
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Biochemical Assay Reagents
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Others
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Bis-Cbz-cyclen is a bifunctional chelator. Bifunctional chelating agents are used to stably link the radiometal to the carrier moiety of the radiopharmaceutical .
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- HY-177894
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Drug Intermediate
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Others
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Fmoc-Asp(OMpe)-Cbz is a drug intermediate that can be used for the synthesis of Fmoc-Asp(OMpe)-OH.
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- HY-126375
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Benzyloxycarbonyl valacyclovir
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Drug Intermediate
HSV
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Infection
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Cbz-Valaciclovir (Benzyloxycarbonyl valacyclovir) can be used to prepare Valaciclovir (HY-17425) and for antiviral research .
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- HY-48321
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ADC Linker
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Cancer
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N-Cbz-glycyl-glycyl-D-phenylalanine is a cleavable ADC linker.
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- HY-116011
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Drug Intermediate
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Cancer
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N,N'-bis-Cbz-β-Alethine is an active ester used in the synthesis of β-alethine, which induces cell differentiation and has potential anti-tumor applications. β-Alethine is synthesized by removing the carbobenzoxy (CBZ) groups with hydrogen bromide in glacial acetic acid.
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- HY-W190968
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PROTAC Linkers
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Cancer
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Cbz-PEG2-bromide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140490
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PROTAC Linkers
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Cancer
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Cbz-N-PEG10-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-143832
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PROTAC Linkers
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Cancer
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Cbz-PEG5-Br is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140443
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PROTAC Linkers
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Cancer
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Cbz-aminooxy-PEG8-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-W904851
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PROTAC Linkers
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Cancer
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Boc-Piperidine-piperazine-Cbz is a PROTAC linker that can be used in the synthesis of ZLC491 (HY-168162) .
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- HY-159617
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PROTAC Linkers
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Cancer
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Cbz-Pip-2C-Pip-C-Pip is a PROTAC linker. Cbz-Pip-2C-Pip-C-Pip can be used for synthesis PROTAC Cbl-b-IN-1 (HY-159608) .
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- HY-W588712
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- HY-163382
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Beta-lactamase
Cholinesterase (ChE)
Amyloid-β
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Neurological Disease
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Cbz-Gly-Pro-Ala-O-cinnamyl (compound 25) is a small peptide targeting BACE-1 and AChE with the IC50 values of 0.02 μM and 1 μM, respectively. Cbz-Gly-Pro-Ala-O-cinnamyl shows neuroprotective effect and can be used for study of Alzheimer’s disease .
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- HY-129352
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ADC Linker
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Cancer
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Cbz-Phe-(Alloc)Lys-PAB-PNP is an cleavable linker for antibody-drug conjugates (ADC) design.
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- HY-140491
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PROTAC Linkers
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Cancer
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Cbz-N-amido-PEG20-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140238
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PROTAC Linkers
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Cancer
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Cbz-N-PEG15-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140444
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PROTAC Linkers
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Cancer
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Cbz-aminooxy-PEG8-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-172790
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COX
Lipoxygenase
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Inflammation/Immunology
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Cbz-(S,S)-Pro-Pro-allyl (compound 1a) is a dual inhibitor of cyclooxygenase-2 and 5-lipoxygenase with IC50 values of 0.146 nM, 0.003 nM, 0.64 nM for COX-1, COX-2, 5-LOX, respectively. Cbz-(S,S)-Pro-Pro-allyl has anti-inflammatory activity .
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- HY-47812
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- HY-W019796
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG4-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-130443
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG6-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-133359
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG24-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-133360
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG36-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135919
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG5-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135942
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG8-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-133357
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG10-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-W348348
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Biochemical Assay Reagents
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Others
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CbzNH-PEG3-CH2CH2NH2 is a PEG linker containing an amine group and a benzyl (Cbz) protecting group. The hydrophilic PEG spacer increases the water solubility of a compound in aqueous media. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde), etc. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
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- HY-W403327
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Biochemical Assay Reagents
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Others
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CbzNH-PEG4-CH2COOH is a PEG linker containing an carboxylic acid (CO2H) group and a benzyl (Cbz) protecting group. The hydrophilic PEG spacer increases the water solubility of a compound in aqueous media. The terminal carboxylic acid is reactive with primary amine groups in the presence of activators (e.g. HATU) forming a stable amide bond. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
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- HY-W653882
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- HY-W1119955
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- HY-179708
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Ser/Thr Protease
Factor Xa
SARS-CoV
Influenza Virus
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Infection
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Cbz-QFR-kbt is a ketone-based benzothiazole ketone inhibitor of TMPRSS2, with an IC50 value of 0.42 nM. Cbz-QFR-kbt also has inhibitory activity against Matriptase, Hepsin, HGFA, and Factor Xa, with IC50 values of 1, 1.3, 85, and 85 nM respectively. Cbz-QFR-kbt shows significant inhibitory effects against SARS-CoV-2 and H1N1 (IC50 = 60 nM). Cbz-QFR-kbt can be used in antiviral research .
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- HY-173261
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Biochemical Assay Reagents
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Others
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Tri-GalNAc(OAc)3-Cbz 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-155665
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ADC Linker
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Cancer
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NH2-CH-CONH-CH2-O-CH2-Cbz (Page 3, Compound E) is an ADC linker that can be used for the synthesis of antibody-conjugated active molecules (ADC) .
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- HY-W946552
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG-alkyne is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-185385
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Drug Intermediate
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Others
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SNA C(Bz) amidite is a phosphoramide monomer that can be used to synthesize oligonucleotides.
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- HY-44312
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Biochemical Assay Reagents
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Others
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Cbz-TRIS tri-acid is a small molecule compound containing several functional groups, including a carbamate group, a tris group, and three carboxylic acid groups.
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- HY-W160298
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Biochemical Assay Reagents
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Others
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N-Cbz-7-Aminoheptanoic acid is a six carbon linker containing an carboxylic acid (CO2H) group and a benzyl (Cbz) protecting group. The terminal carboxylic acid is reactive with primary amine groups in the presence of activators (e.g. EDC, or HATU) forming a stable amide bond. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
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- HY-W580126
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG3-tosyl is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-W583812
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PROTAC Linkers
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Cancer
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Cbz-PEG2-prop-1-yne is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-W583811
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PROTAC Linkers
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Cancer
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Cbz-PEG3-prop-1-yne is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-W415279
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PROTAC Linkers
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Cancer
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Cbz-NH-C4-O-NH2 is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-W793322
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PROTAC Linkers
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Cancer
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Cbz-NH-C2-PEG3-Br is a PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-W1121768
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- HY-49453
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PROTAC Linkers
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Cancer
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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 .
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- HY-W353728
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N-CBZ-Tyramine
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Glutaminase
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Metabolic Disease
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N-Carbobenzoxytyramine (N-CBZ-Tyramine), a carbobenzoxy derivatives of amino acid, is a competitive inhibitor of glutaminase activity .
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- HY-W019226
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ADC Linker
PROTAC Linkers
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Cancer
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Methyl 1-Cbz-azetidine-3-carboxylate is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Methyl 1-Cbz-azetidine-3-carboxylate is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1
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- HY-W097167
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- HY-156810
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ADC Linker
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Cancer
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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) .
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- HY-400676
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ADC Linker
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Cancer
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NH2-PEG4-GGFG-CH2-O-CH2-Cbz is a reactant for the synthesis of ADC linker and is used to synthesize Antibody-Drug Conjugates (ADCs) .
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- HY-168197
-
|
|
PROTACs
|
Cancer
|
|
Thalidomide-F-piperidine-piperazine-Cbz Conjugate 110 is a conjugate of E3 ligase and linker for the synthesis of CDK12/13 PROTAC degrader (HY-168162) .
|
-
- HY-75332
-
|
D-CBZ phenylglycine
|
Amino Acid Derivatives
|
Others
|
|
Z-D-Phg-OH (D-Cbz phenylglycine) is a N-blocked amino acids with Kd values of 390 μM and 323 μM for tBuCQN and tBuCQD, respectively .
|
-
- HY-141148
-
|
|
Drug-Linker Conjugates for ADC
|
Cancer
|
|
7-O-(Cbz-N-amido-PEG4)-paclitaxel is a PEG-class Drug-linker conjugates for ADC, containing a paclitaxel moiety and a amino group. The amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. 7-O-(Cbz-N-amido-PEG4)-paclitaxel can be used in the synthesis of Antibody-Drug Conjugates (ADCs) .
|
-
- HY-W097106
-
|
|
Drug Isomer
|
Neurological Disease
|
|
(S)-3-N-Cbz-Amino-succinimide (Compound 1d) is an antiepileptic agent that can inhibit pentylenetetrazole (PTZ) and maximal electroshock (MES)-induced tonic convulsions in mice .
|
-
- HY-W058001
-
|
|
PROTAC Linkers
|
Cancer
|
|
1-Cbz-Azetidine-3-CH2NH2 is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-32685
-
-
- HY-156896
-
|
|
Drug-Linker Conjugates for ADC
|
Cancer
|
|
Val-Cit-amide-Cbz-N(Me)-Maytansine is an antibody and bispecific antigen-binding mol. that bind hepatocyte growth factor receptor c-Met (MET) or antibody-drug conjugates (ADCs) .
|
-
- HY-W097168
-
|
N-CBZ-DL-histidine
|
Amino Acid Derivatives
|
Others
|
|
Z-DL-His-OH (N-Cbz-DL-histidine) (Compound 14) is a Histidine derivative. Z-DL-His-OH shows no inhibitory effect on the root growth of rapeseed .
|
-
- HY-P1759B
-
|
Z-FR-AMC TFA
|
Cathepsin
|
Others
|
|
N-CBZ-Phe-Arg-AMC (Z-FR-AMC) TFA is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
|
-
- HY-W777099
-
-
- 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-W011092
-
|
Nα-Boc-Nδ-CBZ-L-ornithine
|
Biochemical Assay Reagents
|
Others
|
|
Boc-Orn(Z)-OH (Nα-Boc-Nδ-Cbz-L-ornithine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research .
|
-
- HY-W008753
-
|
N-CBZ-L-valine
|
Biochemical Assay Reagents
Drug Intermediate
Amino Acid Derivatives
|
Infection
|
|
Z-L-Val-OH (N-Cbz-L-valine) is an amino acid derivative and key intermediate in organic synthesis. Z-L-Val-OH can be used in the synthesis of anti-cytomegalovirus compounds and peptide inhibitors of human spleen plasminogen activator (SFP) and human leukocyte elastase-like protease (ELP) .
|
-
- HY-W011024
-
|
|
Biochemical Assay Reagents
|
Others
|
|
(2R,3S)-N-Cbz-6-oxo-2,3-diphenylmorpholine is a chiral building block, which can be used in the stereoselective synthesis of fluorescent and non-fluorescent amino acids .
|
-
- HY-173459
-
|
|
SARS-CoV
|
Infection
|
|
N-0920 is a potent TMPRSS2 inhibitor with an IC50 of 0.35 nM. N-0920 effectively inhibits SARS-CoV-2 variants EG.5.1 and JN.1 entry in Calu-3 cells, with picomolar EC50s values of 300 pM and 90 pM, respectively .
|
-
- HY-P11476
-
-
- HY-D3169
-
|
|
Fluorescent Dye
Caspase
|
Inflammation/Immunology
|
|
IETDC is a caspase 8 probe substrate. IETDC is cleaved by activated caspase 8 to release D-cysteine. The D-cysteine released by IETDC binds to HCBT to generate firefly luciferin in situ, accompanied by a bioluminescent signal produced by H2O2-mediated release of 6-hydroxy-2-cyanobenzothiazole. IETDC is applicable to studies related to acute inflammation .
|
-
- HY-151468
-
|
|
Fluorescent Dye
|
Others
|
|
AIECbz-LD-C7 is an aggregation-induced emission (AIE) probe based on the conjugation of quinoline-malononitrile (QM) and carbazole. AIECbz-LD-C7 has excellent LD-specificity. AIECbz-LD-C7 can be used for tracking the dynamic changes of LDs and studying the association between LDs and lysosome/endoplasmic reticulum (ER) .
|
-
- HY-W003991
-
-
- HY-P2269
-
|
|
Drug Derivative
|
Cancer
|
|
MAIT-203, a cyclopentyalanin-derived peptidomimetic, potently inhibits the interaction of adenomatous polyposis coli (APC) and Asef (RhoGEF4), but not APC-Sam68 or APC-striatin interactions. MAIT-203 binds APC-ARM with a Ki of 0.015 μM and a Kd of 0.036 μM. MAIT-203 significantly represses the migration and invasion of colorectal cancer cells.
|
-
- HY-P2269A
-
|
|
Drug Derivative
|
Cancer
|
|
MAIT-203 acetate is a cyclopentyalanin-derived peptidomimetic, potently inhibits the interaction of adenomatous polyposis coli (APC) and Asef (RhoGEF4), but not APC-Sam68 or APC-striatin interactions. MAIT-203 acetate binds APC-ARM with a Ki value of 0.015 μM and aKd value of 0.036 μM. MAIT-203 acetate significantly represses the migration and invasion of colorectal cancer cells .
|
-
- HY-W800833
-
|
|
Biochemical Assay Reagents
|
Others
|
|
Benzyl N-[2-(prop-2-enamido)ethyl]carbamate is a short aliphatic linker featuring a Cbz-protected amine and an acrylamide. Acrylamide is a Michael acceptor which is a good Michael acceptor which can be used in thiol-based bioconjugation or polymerization. Meanwhile, the Cbz protecting group can be removed using Pd-C hydrogenation to reveal a free amine that can participate in a wide variety of reactions such as couplings or reductive amination.
|
-
- HY-W060779
-
-
- HY-W591969
-
|
|
Biochemical Assay Reagents
|
Others
|
|
Benzyl (6-oxohexyl)carbamate is a linker containing an aldehyde group and a benzyl (Cbz) protecting group. The aldehyde can react with hydrazine or hydrazide to form a hydrolytic acyl hydrozone linkage. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
|
-
- HY-W451433
-
|
|
Biochemical Assay Reagents
|
Others
|
|
OTs-PEG1-NHCbz is a PEG linker containing a tosyl group and benzyl (Cbz) protecting group. The hydrophilic PEG spacer increases the water solubility of the compound in aqueous media. The tosyl group is a very good leaving group for nucleophilic substitution reactions. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
|
-
- HY-P3106
-
|
(Z-Ala-Ala-Ala-Ala)2Rhodamine110; bis-CBZ-L-alanyl-L-arginine amide Rhodamine 110
|
Fluorescent Dye
|
Others
|
|
(Z-Ala-Ala-Ala-Ala)2Rh110 is a sensitive fluorogenic elastase substrate. The colorless and nonfluorescent (Z-Ala-Ala-Ala-Ala)2Rh110 is selectively cleaved by elastase to yield the highly fluorescent compound rhodamine 110, which can be analyzed with an excitation wavelength of 485 nm and emission wavelength of 525 nm.
|
-
| Cat. No. |
Product Name |
Type |
-
- HY-D3169
-
|
|
Fluorescent Dyes
|
|
IETDC is a caspase 8 probe substrate. IETDC is cleaved by activated caspase 8 to release D-cysteine. The D-cysteine released by IETDC binds to HCBT to generate firefly luciferin in situ, accompanied by a bioluminescent signal produced by H2O2-mediated release of 6-hydroxy-2-cyanobenzothiazole. IETDC is applicable to studies related to acute inflammation .
|
| Cat. No. |
Product Name |
Type |
-
- HY-W016042
-
|
|
Biochemical Assay Reagents
|
|
N-Cbz-Hydroxy-L-proline is a chiral N-Cbz-protected amino acid derivative. N-Cbz-Hydroxy-L-proline is commonly used in the synthesis of polypeptides and pharmaceutical intermediates. N-Cbz-Hydroxy-L-proline undergoes decarboxylation under AlCl3/HFIP conditions .
|
-
- HY-32685
-
-
- HY-P1759A
-
|
Z-FR-AMC hydrochloride
|
Biochemical Assay Reagents
|
|
N-CBZ-Phe-Arg-AMC (Z-FR-AMC) hydrochloride is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
|
-
- HY-W008753
-
|
N-CBZ-L-valine
|
Biochemical Assay Reagents
|
|
Z-L-Val-OH (N-Cbz-L-valine) is an amino acid derivative and key intermediate in organic synthesis. Z-L-Val-OH can be used in the synthesis of anti-cytomegalovirus compounds and peptide inhibitors of human spleen plasminogen activator (SFP) and human leukocyte elastase-like protease (ELP) .
|
-
- HY-W402032
-
|
|
Biochemical Assay Reagents
|
|
Bis-Cbz-cyclen is a bifunctional chelator. Bifunctional chelating agents are used to stably link the radiometal to the carrier moiety of the radiopharmaceutical .
|
| Cat. No. |
Product Name |
Target |
Research Area |
-
- HY-136626
-
|
CBZ-Ala-Ala-Asn-AMC
|
Fluorescent Dye
|
Cancer
|
|
Z-Ala-Ala-Asn-AMC (Cbz-Ala-Ala-Asn-AMC) is the legumain substrate. Overexpressed legumain in 293 HEK-Leg cells potently cleaved CBZ-Ala-Ala-Asn-AMC .
|
-
- HY-P1759
-
|
Z-FR-AMC
|
Cathepsin
|
Others
|
|
N-CBZ-Phe-Arg-AMC (Z-FR-AMC) is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
|
-
- HY-P1759B
-
|
Z-FR-AMC TFA
|
Cathepsin
|
Others
|
|
N-CBZ-Phe-Arg-AMC (Z-FR-AMC) TFA is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
|
-
- HY-W011750
-
-
- HY-134113
-
|
CBZ-Chromozym TH
|
Biochemical Assay Reagents
|
Others
|
|
Z-Gly-Pro-Arg-pNA (z-GPR-pNA) is a photometric substrate in Prostate-Specific Antigen (PSA) activation protease assays. Z-Gly-Pro-Arg-pNA (z-GPR-pNA) can be used for the test of trypsin activity .
|
-
- HY-P3106
-
|
(Z-Ala-Ala-Ala-Ala)2Rhodamine110; bis-CBZ-L-alanyl-L-arginine amide Rhodamine 110
|
Fluorescent Dye
|
Others
|
|
(Z-Ala-Ala-Ala-Ala)2Rh110 is a sensitive fluorogenic elastase substrate. The colorless and nonfluorescent (Z-Ala-Ala-Ala-Ala)2Rh110 is selectively cleaved by elastase to yield the highly fluorescent compound rhodamine 110, which can be analyzed with an excitation wavelength of 485 nm and emission wavelength of 525 nm.
|
-
- HY-78897
-
-
- HY-P5027
-
-
- HY-W009503
-
-
- HY-P5042
-
|
|
Peptides
|
Others
|
|
Cbz-Tyr-Ala-OH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
|
-
- HY-W003991
-
-
- HY-W013905
-
-
- HY-76317
-
|
N-CBZ-DL-proline; DL-CBZ-Proline
|
Amino Acid Derivatives
|
Others
|
|
Z-DL-Pro-OH (N-Cbz-DL-proline) is a proline derivative, can be used for the synthesis of agents or other compounds .
|
-
- HY-75332
-
|
D-CBZ phenylglycine
|
Amino Acid Derivatives
|
Others
|
|
Z-D-Phg-OH (D-Cbz phenylglycine) is a N-blocked amino acids with Kd values of 390 μM and 323 μM for tBuCQN and tBuCQD, respectively .
|
-
- HY-P5024
-
|
NSC 333754
|
Peptides
|
Others
|
|
Cbz-Ile-Pro-OH (NSC 333754) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
|
-
- HY-P10198
-
-
- HY-I1061
-
-
- HY-400312
-
-
- HY-P5040
-
-
- HY-P5008
-
|
CBZ-Asn-Gly; Z-Asn-Gly-OH
|
Peptides
|
Others
|
|
Cbz-Asn-Gly-OH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
|
-
- HY-P5012
-
|
NSC 186902
|
Peptides
|
Others
|
|
Cbz-Glu-Gly-OH (NSC 186902) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
|
-
- HY-173459
-
|
|
SARS-CoV
|
Infection
|
|
N-0920 is a potent TMPRSS2 inhibitor with an IC50 of 0.35 nM. N-0920 effectively inhibits SARS-CoV-2 variants EG.5.1 and JN.1 entry in Calu-3 cells, with picomolar EC50s values of 300 pM and 90 pM, respectively .
|
-
- HY-P10213
-
-
- HY-P2269A
-
|
|
Drug Derivative
|
Cancer
|
|
MAIT-203 acetate is a cyclopentyalanin-derived peptidomimetic, potently inhibits the interaction of adenomatous polyposis coli (APC) and Asef (RhoGEF4), but not APC-Sam68 or APC-striatin interactions. MAIT-203 acetate binds APC-ARM with a Ki value of 0.015 μM and aKd value of 0.036 μM. MAIT-203 acetate significantly represses the migration and invasion of colorectal cancer cells .
|
-
- HY-P2269
-
|
|
Drug Derivative
|
Cancer
|
|
MAIT-203, a cyclopentyalanin-derived peptidomimetic, potently inhibits the interaction of adenomatous polyposis coli (APC) and Asef (RhoGEF4), but not APC-Sam68 or APC-striatin interactions. MAIT-203 binds APC-ARM with a Ki of 0.015 μM and a Kd of 0.036 μM. MAIT-203 significantly represses the migration and invasion of colorectal cancer cells.
|
-
- HY-W060779
-
-
- HY-P11476
-
-
- HY-D3169
-
|
|
Fluorescent Dye
Caspase
|
Inflammation/Immunology
|
|
IETDC is a caspase 8 probe substrate. IETDC is cleaved by activated caspase 8 to release D-cysteine. The D-cysteine released by IETDC binds to HCBT to generate firefly luciferin in situ, accompanied by a bioluminescent signal produced by H2O2-mediated release of 6-hydroxy-2-cyanobenzothiazole. IETDC is applicable to studies related to acute inflammation .
|
| Cat. No. |
Product Name |
Chemical Structure |
-
- HY-B0246S
-
|
|
|
Carbamazepine-d10 is the deuterium labeled Carbamazepine. Carbamazepine (CBZ), a sodium channel blocker, is an anticonvulsant agent .
|
-
-
- HY-B0246S2
-
|
|
|
Carbamazepine-d8 is the deuterium labeled Carbamazepine. Carbamazepine, a sodium channel blocker, is an anticonvulsant agent, with an IC50 of 131 μM .
|
-
-
- HY-B0246S3
-
|
|
|
Carbamazepine-(Ph)d8 (CBZ-(Ph)d8; NSC 169864-(Ph)d8) is the deuterium labeled Carbamazepine-(Ph) (HY-B0246) .
|
-
-
- HY-B0246S4
-
|
|
|
Carbamazepine-d4 (CBZ-d4) is the deuterium labeled Carbamazepine (HY-B0246) . Carbamazepine is an orally active pressure-sensitive sodium ion channel blocker with an IC50 of 131 μM. Carbamazepine blocks voltage gated Na +, Ca 2+, and K + channels, and is also a HDAC inhibitor (IC50: 2 μM). Carbamazepine is an anticonvulsant and can be used for research of epilepsy and neuropathic pain.
|
-
-
- HY-B0246S1
-
|
|
|
Carbamazepine-d2 is the deuterium labeled Carbamazepine. Carbamazepine, a sodium channel blocker, is an anticonvulsant agent.
|
-
-
- HY-W777099
-
|
|
|
N-Cbz-O-Bzl-L-Glu-S-Bzl-L-Cys-Gly[ 13C2, 15N]-OBzl is the 13C- and 15N-labeled N-Cbz-O-Bzl-L-Glu-S-Bzl-L-Cys-Gly-OBzl.
|
-
-
- HY-W653882
-
|
|
|
Carbamazepine-d2,15N is a deuterated labeled Carbamazepine-d2,15N .
|
-
| Cat. No. |
Product Name |
|
Classification |
-
- HY-173261
-
|
|
|
Azide
|
|
Tri-GalNAc(OAc)3-Cbz is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W1121768
-
|
|
|
Alkynes
|
|
C(Bz)-2-Propargyl amidite 2-O-propargyl C(Bz)-3-phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
|
| Cat. No. |
Product Name |
|
Classification |
-
- HY-W1121768
-
|
|
|
Phosphoramidites
Cytosine
|
|
C(Bz)-2-Propargyl amidite 2-O-propargyl C(Bz)-3-phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
|
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