Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 020104 | Setipiprant | 866460-33-5 | 98% |  |
| Setipiprant is an orally available, selective CRTH2 antagonist. CRTH2 is a G protein- | ||||
| 011921 | SB-705498 | 501951-42-4 | 98% |  |
| SB-705498 is a potent, selective and orally bioavailable transient receptor potential | ||||
| 011917 | SCHEMBL2274423 | 1206194-91-3 | 98% |  |
| Coming soon! | ||||
| 011915 | SSR240612 | 464930-42-5 | 98% |  |
| Coming soon! | ||||
| 011912 | SU14813 | 627908-92-3 | 98% |  |
| SU14813 is an oral, multitargeted tyrosine kinase inhibitor (TKI) targeting vascular | ||||
| 011901 | SDZ 220-581 | 174575-17-8 | 98% |  |
| SDZ 220-581 is a potent, competitive antagonist at the NMDA glutamate receptor subtyp | ||||
| 011815 | SB-649868 | 380899-24-1 | 98% |  |
| Coming soon! | ||||
| 011806 | SGI-110 | 929901-49-5 | 98% |  |
| SGI-110 is a small molecule, DNMT inhibitor with demonstrated activity in restoring s | ||||
| 011313 | SC144 | 895158-95-9 | 98% |  |
| SC144 is the first-in-class orally active small-molecule gp130 inhibitor. | ||||
| 011308 | SKF-86002 | 72873-74-6 | 98% |  |
| SKF-86002 is a potent inhibitor of p38 MAP kinase wit IC50 of 0.5-1 uM. | ||||
| 011304 | SD-208 | 627536-09-8 | 98% |  |
| SD-208 is a potent, orally active ATP-competitive transforming growth factor- recepto | ||||
| 11106 | SCH772984 | 942183-80-4 | 98% |  |
| SCH772984 is a novel, specific inhibitor of ERK1/2 with IC50 of 4 nM and 1 nM, respec | ||||
| 010805 | Savolitinib(Volitinib) | 1313725-88-0 | 98% | -cas-1313725-88-0.png) |
| Savolitinib is an orally bioavailable inhibitor of the c-Met receptor tyrosine kinase | ||||
| 010804 | SF1126 | 936487-67-1 | 98% |  |
| SF1126 is a water soluble, small-molecule prodrug containing the pan-PI3K/mTOR inhibi | ||||
| 010601 | Staurosporine | 62996-74-1 | 98% |  |
| Staurosporine is a prototypical potent ATP-competitive kinase inhibitor with IC50 of | ||||
| 010438 | SCH900776 S-isomer | 891494-64-7 | 98% |  |
| SCH900776 (S-isomer) is the S-isomer form of SCH900776(HY-15532), which is a potent, | ||||
| 010427 | SB 242084 | 181632-25-7 | 98% |  |
| SB 242084 is a 5-HT2C receptor antagonist(pKi=9.0) that displays 158- and 100-fold se | ||||
| 010425 | SB 415286 | 264218-23-7 | 98% |  |
| SB 415286 is a potent and selective cell-permeable, ATP-competitive inhibitor of GSK3 | ||||
| 122945 | SGI-1776 | 1025065-69-3 | 98% |  |
| SGI-1776 is a novel ATP competitive inhibitor of Pim1 with IC50 of 7 nM; 50- and 10-f | ||||
| 122944 | Sonolisib | 502632-66-8 | 98% |  |
| Sonolisib is a small-molecule wortmannin analogue inhibitor of the alpha, gamma, and | ||||
| 122922 | Soraphen A | 122547-72-2 | 98% |  |
| Coming soon! | ||||
| 122921 | Sembragiline | 676479-06-4 | 98% |  |
| Coming soon! | ||||
| 122913 | Saracatinib | 379231-04-6 | 98% |  |
| Saracatinib is an orally available 5-, 7-substituted anilinoquinazoline with anti-inv | ||||
| 122912 | SU11274 | 658084-23-2 | 98% |  |
| SU11274 is a selective Met inhibitor with IC50 of 10 nM, no effects on PGDFR, EGFR or | ||||
| 122831 | STF31 | 724741-75-7 | 98% |  |
| STF31 is a potent glucose transporter 1 (GLUT1). | ||||
| 122802 | SM-164 | 957135-43-2 | 98% |  |
| SM-164 is a potent cell-permeable and bivalent Smac mimetic which bind to a XIAP prot | ||||
| 122518 | SB-742457 ( Intepirdine ) | 607742-69-8 | 98% | _607742-69-8.png) |
| SB-742457(Intepirdine) is a highly selective 5-HT6 receptor antagonist with pKi of 9. | ||||
| 122516 | SNG-1153 | 98% |  | |
| Coming soon! | ||||
| 122504 | SGC0946 | 1561178-17-3 | 98% |  |
| SGC0946 is a highly potent and selective DOT1L methyltransferase inhibitor with IC50 | ||||
| 122503 | (S)-2-Ethylpiperazine dihydrochloride | 128427-05-4 | 98% | -2-Ethylpiperazinedihydrochloride-cas-128427-05-4.png) |
| Coming soon! | ||||