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Cas号索引 1

• 17318-31-9 | SQ22536 (Catalog# : 16122726)SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 M. It can inhibit PGE
• 111540-00-2 | STA-21 (Catalog# : 16122706)STA-21 is a selective STAT3 inhibitor.In cells, STA-21 inhibits Stat3 DNA binding act
• 1335106-03-0 | SR1001 (Catalog# : 6111522)SR1001 is a selective ROR and ROR inverse agonist; suppresses TH17 cell differentiati
• 1324003-64-6 | S1P1 Agonist III (Catalog# : 61119)S1P1 Agonist III is a potent and orally active S1P1 agonist with EC50 of 18 nM; no ac
• 1186222-89-8 | 4SC-202 (Catalog# : 611937)4SC-202 is an orally available potent HDACi specific for class I HDAC isoenzymes(NO H
• 1454585-06-8 | SR-3029 (Catalog# : 611915)SR 3029 is a potent and highly specific CK1/CK1 inhibitor with the IC50 of 97 nM.SR-3
• 1456632-40-8 | SH-4-54 (Catalog# : 16071406)SH-4-54 is a potent STAT inhibitor with KD of 300 nM and 464 nM for STAT3 and STAT5,
• 1230487-00-9 | Siponimod (Catalog# : 16071404)Siponimod, also known as BAF-312, is a a potent and orally selective S1P Receptor Mod
• 1116743-46-4 | SAR125844 (Catalog# : 16071023)SAR125844 is a potent and highly selective c-Met inhibitor with potential antineoplas
• 1093403-33-8 | SRT2104 (Catalog# : 16071014)SRT2104, also known as GSK2245840, is a novel, first-in-class, highly selective small
• 1359164-11-6 | SR-2211 (Catalog# : 16071002)SR-2211
• 1022150-57-7 | SGX-523 (Catalog# : 16070912)SGX523 is a novel, ATP-competitive kinase inhibitor remarkable for its exquisite sele
• 160162-42-5 | SR 11302 (Catalog# : 16070908)SR 11302
• 1239875-86-5 | SGI 7079 (Catalog# : 16070902)SGI 7079
• 125941-87-9 | SCH23390 (Catalog# : 16070103)SCH23390
• 130495-35-1 | SKF-96365 HCl (Catalog# : 16062905)SKF-96365 is a selective TRPC channel blocker. SKF-96365 activates cytoprotective aut
• 163169-15-1 | (S)-4-tert-Butyl-2-[(SP)-2-(diphenylphosphino)ferrocenyl]-2-oxazoline (Catalog# : 16062106)(S)-4-tert-Butyl-2-[(SP)-2-(diphenylphosphino)ferrocenyl]-2-oxazoline
• 160098-96-4 | SCH-58261 (Catalog# : 16060802)SCH-58261 is a potent and selective adenosine A(2A) receptor antagonist. SCH-58261 is
• 151823-14-2 | Sapacitabine (Catalog# : 031703)Sapacitabine is an orally bioavailable pyrimidine analogue prodrug with potential ant
• 149845-06-7 | Saquinavir Mesylate (Catalog# : 031701)Saquinavir mesylate is an HIV protease inhibitor which acts as an analog of an HIV pr
• 1379686-30-2 | SR9009 (Catalog# : 030908)Coming soon!
• 1206194-91-3 | SCHEMBL2274423 (Catalog# : 011917)Coming soon!
• 174575-17-8 | SDZ 220-581 (Catalog# : 011901)SDZ 220-581 is a potent, competitive antagonist at the NMDA glutamate receptor subtyp
• 1313725-88-0 | Savolitinib(Volitinib) (Catalog# : 010805)Savolitinib is an orally bioavailable inhibitor of the c-Met receptor tyrosine kinase
• 181632-25-7 | SB 242084 (Catalog# : 010427)SB 242084 is a 5-HT2C receptor antagonist(pKi=9.0) that displays 158- and 100-fold se
• 1025065-69-3 | SGI-1776 (Catalog# : 122945)SGI-1776 is a novel ATP competitive inhibitor of Pim1 with IC50 of 7 nM; 50- and 10-f
• 122547-72-2 | Soraphen A (Catalog# : 122922)Coming soon!
• 1561178-17-3 | SGC0946 (Catalog# : 122504)SGC0946 is a highly potent and selective DOT1L methyltransferase inhibitor with IC50
• 128427-05-4 | (S)-2-Ethylpiperazine dihydrochloride (Catalog# : 122503)Coming soon!
• 1221411-72-8 | SP-420 (Catalog# : 122304)SP-420 is an orally active small molecule that selectively binds iron and removes it