Products
| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 2073103 | Remibrutinib ( LOU064 ) | 1787294-07-8 | 98% Min. |  |
| Remibrutinib ( LOU064 ) is a Potent and Highly Selective Covalent Inhibitor of Bruton | ||||
| 51608 | SSR128129E | 848318-25-2 | 98% |  |
| SSR128129E is an orally-active and allostericFGFR1inhibitor withIC50of 1.9 M, while n | ||||
| 51803 | Semaxanib (SU5416) | 204005-46-9 | 98% | -cas-204005-46-9.png) |
| Semaxanib (SU5416) is a potent and selectiveVEGFR(Flk-1/KDR) inhibitor withIC50of 1.2 | ||||
| 51802 | TIC10 ( ONC201 ) | 1616632-77-9 | 99.85% |  |
| TIC10 ( ONC201 ), Bulk in stock, contact us by email for detailed quotation.ONC201/TI | ||||
| 51607 | VE-822 ( Berzosertib ) | 1232416-25-9 | ≧98.0% | _1232416-25-9.png) |
| VE-822(Berzosertib), an analogue of VE-821 with increased potency and selectivity aga | ||||
| 52003 | Zosuquidar trihydrochloride | 167465-36-3 | 99% | _167465-36-3.png) |
| zosuquidar trihydrochloride is adifluorocyclopropyl quinoline. Zosuquidar trihydrochl | ||||
| 52002 | K-7174 dihydrochloride | 191089-60-8 | 98% |  |
| K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of | ||||
| 51910 | TRV130 ( Oliceridine ) | 1401031-39-7 | ≧98.0% | _1401031-39-7.png) |
| TRV 130 Hcl is a novel -opioid receptor (MOR) G protein-biased ligand; elicits robust | ||||
| 52105 | SNS-032 ( BMS-387032 ) | 345627-80-7 | 98% | _345627-80-7.png) |
| SNS-032 has firstly been described as a selective inhibitor ofCDK2withIC50of 48 nM an | ||||
| 51614 | AMG-925 | 1401033-86-0 | 98% |  |
| AMG925, Bulk in stock, contact us by email for detailed quotation.AMG-925 is a potent | ||||
| 52026 | AMG-319 | 1608125-21-8 | 98% |  |
| AMG 319 is an investigational, highly selective, small molecule inhibitor of PI3K tha | ||||
| 62502 | TG02 ( SB1317 ) | 937270-47-8 | ≧98.0% | _937270-47-8.png) |
| SB1317 (TG02) is a novel small molecule potent CDK/JAK2/FLT3 inhibitor. SB1317 was so | ||||