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Chemical Structure Cat. No. Product Name CAS No.
DBCO-NHS Chemical Structure
BCP31927 DBCO-NHS 1353016-71-3
DBCO-NHS is an amine-reactive compound and can be used to modify an amine-containing molecule in organic solvents (limited solubility in aqueous media).
GB1107 Chemical Structure
BCP31924 GB1107 1978336-61-6
GB1107 is a potent, selective, orally active galectin-3 inhibitor with Kd of 37 nM. GB1107 Inhibits Lung Adenocarcinoma Growth and Augments Response to PD-L1 Blockade.
AB-680 Chemical Structure
BCP31923 AB-680 2105904-82-1
AB-680 is highly potent, reversible and selective small molecule inhibitor of CD73 (an ecto-nucleotidase), with a Ki of 4.9 pM for hCD73, displays >10,000-fold selectivity over related ecto-nucleotidases CD39. Anti-tumor activity.
BRD0539 Chemical Structure
BCP31922 BRD0539 1403838-79-8
BRD0539 is a SpCas9 inhibitor.
OSMI-4 Chemical Structure
BCP31917 OSMI-4 2260791-14-6
OSMI-4 is a low nanomolar O-GlcNAc transferase (OGT) inhibitor, with an EC50 of 3 μM in cells.
Tecarfarin Chemical Structure
BCP31892 Tecarfarin 867257-26-9
Tecarfarin (ATI-5923) is an orally active and non-competitive vitamin K epoxide reductase (VKOR) antagonist, and impairs the activation of the vitamin K-dependent clotting factors II, VII, IX and X. Tecarfarin has the antithrombotic activity .
Boc-Thr(Fmoc-Leu)-OH Chemical Structure
BCP15536 Boc-Thr(Fmoc-Leu)-OH 944283-26-5
AM-92016 Chemical Structure
BCP31857 AM-92016 178894-81-0
AM92016 is a specific blocker of the time dependent delayed rectifier potassium current. AM92016 does not show any β-adrenoceptor blocking activity.
Tetrahydrouridine Chemical Structure
BCP31863 Tetrahydrouridine 18771-50-1
Tetrahydrouridine is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine.
AM-92016 hydrochloride Chemical Structure
BCP31856 AM-92016 hydrochloride 133229-11-5
AM-92016 hydrochloride is a specific blocker of rectifier potassium current (IK). AM-92016 hydrochloride delays rectifier potassium channel (IK), repolarizes the membrane thereby restricting the duration of the nerve impulse thereby restricting the duration of the nerve impulse.
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