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Chemical Structure Cat. No. Product Name CAS No.
GSK2256294A Chemical Structure
BCP46295 GSK2256294A 1142090-23-0
GSK2256294A is a potent and selective sEH inhibitor, which is in investigation in patients with endothelial dysfunction or abnormal tissue repair, such as diabetes, wound healing or COPD. GSK2256294 exhibited potent cell-based activity, a concentration-dependent inhibition of the conversion of 14,15-EET to 14,15-DHET in human, rat and mouse whole blood in vitro, and a dose-dependent increase in the LTX/LTX diol ratio in rat plasma following oral administration.
MNK1/2-IN-5 Chemical Structure
BCP46296 MNK1/2-IN-5 1426928-20-2
MNK1/2-IN-5 is a potent and selective MNK1/2 inhibitor as a therapeutic agent.
SU16F Chemical Structure
BCP46277 SU16F 251356-45-3
SU16F is a potent and selective platelet-derived growth factor receptor ß (PDGFRß) inhibitor.
SGK1-IN-4 Chemical Structure
BCP46276 SGK1-IN-4 1628048-93-0
SGK1-IN-4 is a highly selective, orally active SGK1 inhibitor.
CJ033466 Chemical Structure
BCP46275 CJ033466 519148-48-2
CJ-033466 is a Serotonin 5-HT4 Receptor Agonist.
SB-747651A Chemical Structure
BCP46274 SB-747651A 607372-46-3
SB-747651A is a specific mitogen- and stress-activated kinase 1 (MSK1) inhibitor. SB-747651A can be used for the research of inflammation.
SB-747651A dihydrochloride Chemical Structure
BCP46273 SB-747651A dihydrochloride 1781882-72-1
SB-747651A dihydrochloride is a potent MSK1 inhibitor; also inhibiting other AGC group kinases.
Azidamfenicol Chemical Structure
BCP46271 Azidamfenicol 13838-08-9
Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic. Azidamfenicol inhibits ribosomal peptidyltransferase (Ki=22 µM).
CDK4/6-IN-6 Chemical Structure
BCP46270 CDK4/6-IN-6 2380321-51-5
CDK4/6-IN-6 is a potent CDK4/CDK6 inhibitor with a Ki of 0.6 nM and 13.9 nM for CDK4/Cyclin D1 and CDK6/Cyclin D3, respectively.
GLUT inhibitor-1 Chemical Structure
BCP46268 GLUT inhibitor-1 2421141-40-2
GLUT inhibitor-1 is a potent and orally active inhibitor of glucose transporters, targeting both GLUT1 and GLUT3 , with IC 50 s of 242 nM and 179 nM, respectively.
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