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Chemical Structure Cat. No. Product Name CAS No.
Thalidomide Chemical Structure
BCP19772 Thalidomide 50-35-1
Thalidomide is initially promoted as a sedative, inhibits ereblon (CRBN), a part of the cullin-4 E3 ubiquitin ligase complex CUL4-RBX1-DDB1, with a Kd of ∼250 nM, and has immunomodulatory, anti-inflammatory and anti-angiogenic cancer properties.
C25-140 Chemical Structure
BCP30323 C25-140 1358099-18-9
C25-140 is the first in class protein-protein interaction inhibitor of a RING-E3 ligase (TRAF6) / E2 enzyme (Ubc13) binding.
RP-54745 Chemical Structure
BCP30814 RP-54745 135330-08-4
RP 54745 is an inhibitor of macrophage stimulation and interleukin-1 production, and a potential antirheumatic compound.
AMZ30 Chemical Structure
BCP30812 AMZ30 1313613-09-0
AMZ30 is a selective, covalent inhibitors of protein phosphatase methylesterase-1(PME-1; IC50=600 nM); selectively inactivates PME-1 and reduces the demethylated form of PP2A in living cells.
Bax channel blocker Chemical Structure
BCP30816 Bax channel blocker 335165-68-9
Bax channel blocker is a direct allosteric inhibitor of BAX.
Uridine-5'-triphosphoric acid trisodium salt Chemical Structure
BCP30809 Uridine-5'-triphosphoric acid trisodium salt 19817-92-6
Uridine 5’-Triphosphate Trisodium Salt is a polyphosphate analogue of uridine that is used in the synthesis of agonists at the G-protein-coupled P2Y receptors.
Uridine-5'-diphosphate disodium salt Chemical Structure
BCP30808 Uridine-5'-diphosphate disodium salt 27821-45-0
UDP disodium salt is an endogenous P2Y receptor agonist which preferentially activates P2Y6.
Vimirogant Chemical Structure
BCP30659 Vimirogant 1802706-04-2
Vimirogant is a RORγ inhibitor extracted from patent US 9481674 B1, has a Ki of <100 nM.
SR-0987 Chemical Structure
BCP29012 SR-0987 303126-97-8
SR-0987 is a T cell-specific RORγ (RORγt) agonist.
GSK2981278 Chemical Structure
BCP17156 GSK2981278 1474110-21-8
GSK 2981278 (GSK2981278) is a potent, highly selective RORγ/RORγt inhibitor that potently inhibits IL-17A and IL-22 protein secretion in human peripheral T cell with IC50 of 3.2 nM.
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