449 Results for "

Alkyl

" in MedChemExpress (MCE) Product Catalog:
Products (449)

449 Results for "Alkyl" in MCE Product Catalog:

37
37 Publications Verification
Cat. No.: HY-118411
CAS No.: 61135-33-9
Purity:  99.78%
Synonyms: EdU
Target:  

PROTAC Linkers

Research Areas:  

Cancer

5-Ethynyl-2'-deoxyuridine (EdU), a thymidine analogue, is incorporated into cellular DNA during DNA replication and the subsequent reaction of EdU with a fluorescent azide in a “Click” reaction. EdU staining is a fast, sensitive and reproducible method to study cell proliferation . 5-Ethynyl-2'-deoxyuridine is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs . 5-Ethynyl-2'-deoxyuridine 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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25
25 Cited Publications
Cat. No.: HY-W008574
CAS No.: 51987-99-6
Target:  

PROTAC Linkers

Research Areas:  

Inflammation/Immunology Cancer

TGN-020 is a selective Aquaporin 4 (AQP4) inhibitor with an IC50 of 3.1 μM . TGN-020 is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs .TGN-020 alleviates edema and inhibits glial scar formation after spinal cord compression injury in rats .
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25
25 Cited Publications
Cat. No.: HY-W008574A
CAS No.: 1313731-99-5
Target:  

PROTAC Linkers

Research Areas:  

Inflammation/Immunology Cancer

TGN-020 sodium is a selective Aquaporin 4 (AQP4) inhibitor with an IC50 of 3.1 μM . TGN-020 sodium is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs . TGN-020 sodium alleviates edema and inhibits glial scar formation after spinal cord compression injury in rats .
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9
9 Cited Publications
Cat. No.: HY-130458
CAS No.: 70539-42-3
Purity:  97.45%
Synonyms: EGS crosslinker
Target:  

PROTAC Linkers

Research Areas:  

Cancer

EGNHS is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs .
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7
7 Cited Publications
Cat. No.: HY-B1068
CAS No.: 25301-02-4
Research Areas:  

Metabolic Disease

Tyloxapol is a nonionic liquid polymer of the alkyl aryl polyether alcohol type, used as a surface active stabilizer. Tyloxapol is used to induce hyperlipidemia in animals .
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7
7 Cited Publications
Cat. No.: HY-107608
CAS No.: 71160-24-2
Purity:  ≥98.0%
Synonyms: LTB4; 5(S),12(R)-DiHETE
Leukotriene B4 (LTB4) is known as one of the most potent chemoattractants and activators of leukocytes and is involved in inflammatory diseases. Leukotriene B4 is also an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs .
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7
7 Cited Publications
Cat. No.: HY-W019711
CAS No.: 14371-10-9
trans-Cinnamaldehyde can be used to prepare highly polyfunctionalized furan ring by reaction of alkyl isocyanides with dialkyl acetylenedicarboxylate . trans-Cinnamaldehyde can be used to synthesize trans-cinnamaldehyde -β-cyclodextrin complex, an antimicrobial edible coating that increases the shelf life of fresh-cut fruits .
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6
6 Cited Publications
Cat. No.: HY-140346A
CAS No.: 942518-29-8
Purity:  98.85%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

L-Azidohomoalanine hydrochloride is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs . L-Azidohomoalanine (hydrochloride) 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. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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5
5 Cited Publications
Cat. No.: HY-125878
CAS No.: 2381320-35-8
Purity:  99.89%
Synonyms: SGK3-PROTAC1
Target:  

PROTACs SGK

Research Areas:  

Cancer

PROTAC SGK3 degrader-1 (SGK3-PROTAC1), a chemical probe, is a von Hippel-Lindau ligand-based SKG3 PROTAC composed of a PEG3-C4-OBn (HY-130620) alkyl linker, an SGK3 degrader (red structure), and a VHL ligand (HY-150803, blue structure). PROTAC SGK3 degrader-1 (0.3 μM) induced 50% endogenous SGK3 degradation within 2 hours, and 80% SGK3 degradation was observed at 8 hours, accompanied by loss of phosphorylation of NDRG1 (SGK3 substrate) .
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4
4 Cited Publications
Cat. No.: HY-140335
CAS No.: 82909-47-5
Purity:  ≥95.0%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Alkynyl myristic acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs . Alkynyl myristic acid 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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3
3 Cited Publications
Cat. No.: HY-141336
CAS No.: 40846-94-4
Purity:  ≥98.0%
Synonyms: DL-α-Lipoic acid-NHS
Target:  

PROTAC Linkers

Research Areas:  

Cancer

α-Lipoic acid-NHS is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs .
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3
3 Cited Publications
Cat. No.: HY-Y0525
CAS No.: 2997-92-4
Synonyms: 2,2'-Azodiisobutyramidine dihydrochloride
Research Areas:  

Inflammation/Immunology

AAPH (2,2'-Azodiisobutyramidine dihydrochloride) has an effect of radical generation. AAPH induces oxidative stress and erythrocyte hemolysis . AAPH decomposes at 37°C to generate an alkyl radical, is used as an initiator. In the presence of oxygen, these alkyl radicals will be converted to peroxyl radicals that can cause lipid peroxidation and loss of erythrocyte membrane integrity, which could ultimately lead to hemolysis .
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3
3 Cited Publications
Cat. No.: HY-W040304
CAS No.: 99208-90-9
Synonyms: Alk-C16
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Alkynyl Palmitic Acid (Alk-C16) is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs . Alkynyl Palmitic Acid 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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3
3 Cited Publications
Cat. No.: HY-108634
CAS No.: 105219-56-5
Purity:  99.93%
Synonyms: WEB 2086
Apafant (WEB 2086), a chemical probe, is a potent platelet-activating factor (PAF) antagonist, inhibits PAF binding to human PAF receptors with a Ki of 9.9 nM. Apafant increases the gene expression of PAF-r, α-globin, β-globin, decreases the c-myb gene expression. Apafant shows a protective effect on alkyl-PAF-mediated lethalit .
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2
2 Cited Publications
Cat. No.: HY-140345
CAS No.: 98891-36-2
Purity:  ≥98.0%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

L-Homopropargylglycine is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. L-homopropargylglycine is an amino acid analog of methionine containing an alkyne moiety that can undergo a classic click chemical reaction with azide containing Alexa Fluor .
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2
2 Cited Publications
Cat. No.: HY-140345A
CAS No.: 942518-19-6
Purity:  ≥98.0%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

L-Homopropargylglycine hydrochloride is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. L-homopropargylglycine hydrochloride is an amino acid analog of methionine containing an alkyne moiety that can undergo a classic click chemical reaction with azide containing Alexa Fluor .
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2
2 Cited Publications
Cat. No.: HY-152229
CAS No.: 1510653-27-6
Purity:  ≥98.0%
G0-C14 is a cationic lipid-like compound alkyl-modified polyamidoamine (PAMAM) dendrimer. G0-C14 involves in the preparation of a series of macrophage-targeted nanoparticles (NPs). NPs can be used for agent and vaccine delivery .
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2
2 Cited Publications
Cat. No.: HY-111997
CAS No.: 1799506-07-2
Purity:  96.49%
Synonyms: HaloPROTAC 3
Research Areas:  

Others

VH285-PEG4-C4-Cl (HaloPROTAC 3) is a conjugate of ligands for E3 and 16-atom-length linker. The connector of linker is Halogen group. VH285-PEG4-C4-Cl incorporates the VH285 based VHL ligand and an alkyl/ether-based linker. VH285-PEG4-C4-Cl is a highly potent and efficacious degrader of GFP-HaloTag7 with a DC50 of 19 nM. VH285-PEG4-C4-Cl is able to induce 90 % degradation of GFP-Halotag at 625 nM. VH285-PEG4-C4-Cl binds to VHL with an IC50 of 0.54 μM .
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1
1 Cited Publications
Cat. No.: HY-136159
CAS No.: 117235-10-6
Purity:  ≥95.0%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

3-Mercaptopropanyl-N-hydroxysuccinimide ester is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs .
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1
1 Cited Publications
Cat. No.: HY-W007803
CAS No.: 164365-88-2
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Boc-NH-C4-Br is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs .
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