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Chemical Structure Cat. No. Product Name CAS No.
Methyl 2-ethyl-3-oxopentanoate Chemical Structure
BCP49661 Methyl 2-ethyl-3-oxopentanoate 32493-32-6
N-Boc-1,2,3,6-tetrahydropyridine Chemical Structure
BCP40084 N-Boc-1,2,3,6-tetrahydropyridine 85838-94-4
TH-Z154 Chemical Structure
BCP49660 TH-Z154 2260887-57-6
TH-Z145, a lipophilic bisphosphonate, is a FPPS inhibitor (IC50: 210 nM).
Ninerafaxstat 3HCl Chemical Structure
BCP49659 Ninerafaxstat 3HCl 2311824-72-1
Ninerafaxstat trihydrochloride shifts cellular metabolism to glucose oxidation from fatty acid oxidation. Ninerafaxstat trihydrochloride improves overall mitochondrial respiration and reduces fatty acid oxidation, thereby inhibiting the proliferation and growth of cancer cells.
ZK53 Chemical Structure
BCP49658 ZK53 3031789-26-8
ZK53 is a selective and potent activator of mitochondrial casein hydrolase protease P (HsClpP).ZK53 induces apoptosis and inhibits the hydrolysis of alpha-casein by HsClpP.ZK53 inhibits tumour growth in xenografts and native mouse models.
TH-Z93 Chemical Structure
BCP49657 TH-Z93 2260887-09-8
TH-Z93, a lipophilic bisphosphonate, is a FPPS inhibitor (IC50: 90 nM).
(+)-Perillaldehyde Chemical Structure
BCP49656 (+)-Perillaldehyde 5503-12-8
(+)-Perillaldehyde is a natural product found in Perilla frutescens, Coleus scutellarioides, and other organisms with data available.
(1R,2R)-1,2-Bis(2-hydroxyphenyl)ethylenediamine Chemical Structure
BCP49655 (1R,2R)-1,2-Bis(2-hydroxyphenyl)ethylenediamine 870991-70-1
N-(2-hydroxyethyl)-3-methylquinoxaline-2-carboxamide Chemical Structure
BCP25031 N-(2-hydroxyethyl)-3-methylquinoxaline-2-carboxamide 104634-22-2
Azvudine Chemical Structure
BCP34041 Azvudine 1011529-10-4
Azvudine is a nucleoside reverse transcriptase inhibitor (NRTI), which exhibits inhibtory effects on HIV, HBV and HCV.
5-Chlorothiophene-2-carbonyl chloride Chemical Structure
BCP11850 5-Chlorothiophene-2-carbonyl chloride 42518-98-9
PD1-PDL1 inhibitor 1 Chemical Structure
BCP15801 PD1-PDL1 inhibitor 1 1675201-83-8
PD1-PDL1 inhibitor 1 is an inhibitor of the PD-1 /PD-Ll protein/protein interaction, is an immunomodulator.
Cathelicidin LL 37 (human) Chemical Structure
BCP30243 Cathelicidin LL 37 (human) 154947-66-7
LL-37 is a human cathelicidin that inhibits viral replication and while also playing a role in host defense against infection.
Bobcat339 hydrochloride Chemical Structure
BCP49654 Bobcat339 hydrochloride 2436747-44-1
Bobcat339 hydrochloride is a potent and selective cytosine-based inhibitor of TET enzyme, with the IC50s of 33 μM and 73 μM for TET1 and TET2, respectively.
β-Cyclodextrin Chemical Structure
BCP49653 β-Cyclodextrin 7585-39-9
β-Cyclodextrin is a cyclic polysaccharide composed of seven units of glucose (α-D-glucopyranose) linked by α-(1,4) type bonds. β-Cyclodextrin has often been used to enhance the solubility of agents. β-Cyclodextrin has anti-influenza virus H1N1 activities.
α-Cyclodextrine Chemical Structure
BCP49652 α-Cyclodextrine 10016-20-3
α-Cyclodextrin is a multifunctional, soluble dietary fiber marketed for use as a fiber ingredient.
Hyodeoxycholic acid Chemical Structure
BCP40517 Hyodeoxycholic acid 83-49-8
Hyodeoxycholic acid is a secondary bile acid, one of the metabolic byproducts of intestinal bacteria.
Boc-NH-PEG(3)-COOH Chemical Structure
BCP49651 Boc-NH-PEG(3)-COOH 876345-13-0
Boc-NH-PEG(3)-COOH is a cleavable ADC linker used as a linker for antibody-drug conjugates and a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
Ribavirin Chemical Structure
BCP03777 Ribavirin 36791-04-5
Ribavirin is a nucleoside antimetabolite antiviral agent that blocks nucleic acid synthesis and is used against both RNA and DNA viruses.
Luxdegalutamide Chemical Structure
BCP49650 Luxdegalutamide 2750830-09-0
Luxdegalutamide is an orally active and potent proteolysis targeting chimera (PROTAC) protein degrader. Luxdegalutamide degrades wild-type androgen receptor (AR) but also relevant AR LBD mutants, including the most prevalent AR L702H, H875Y, and T878A mutations.
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