| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 6121401 | Vadadustat ( AKB-6548 ) | 1000025-07-9 | 98% | ![]() |
| Vadadustat (AKB-6548), a novel, titratable, oral hypoxia-inducible factor prolyl hydr | ||||
| 16122906 | Brivaracetam | 357336-20-0 | 98% | ![]() |
| Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra | ||||
| 71161 | SBI0206965 | 1884220-36-3 | 98% | ![]() |
| SBI0206965 is a potent and selective autophagy Kinase ULK1 Inhibitor. Many tumors bec | ||||
| 2017889 | Roluperidone ( CYR-101 ) | 359625-79-9 | 98.0% | ![]() |
| Roluperidone, also known as MIN-101, CYR-101, and MT-210, is a 5-HT2A and sigma 2 rec | ||||
| 121805 | L-778123 hydrochloride | 253863-00-2 | 98% | ![]() |
| L-778123 hydrochloride is an inhibitor of FPTase and GGPTase-I with IC50 of 2 nM and | ||||
| 1711222 | Asciminib ( ABL001 ) | 1492952-76-7 | 99.35% | ![]() |
| Asciminib, Bulk in stock, contact us by email for the quotation. Kg scale intermediat | ||||
| 185235 | Trilaciclib (G1T28) | 1374743-00-6 | >98% | ![]() |
| TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A | ||||
| 188281 | Arimoclomol maleate | 289893-26-1 | 98% | ![]() |
| Arimoclomol, also known as BRX-220, is potentially useful for the treatment of Nieman | ||||
| 1810163 | BMS-986165 | 1609392-27-9 | >99% | ![]() |
| BMS-986165 potently binds to the Tyk2 pseudokinase domain (Ki = 0.02 nM). BMS-986165 | ||||
| 1811121 | DCC-2618 ( Ripretinib ) | 1442472-39-0 | >98% | ![]() |
| Ripretinib, also known as DCC-2618, is a potent, orally active and selective KIT/PDGF | ||||
| 1811211 | Anlotinib HCl ( AL-3818 ) | 1360460-82-7 | ≧98.0% | ![]() |
| Anlotinib is a novel oral tyrosine kinase inhibitor (TKI) targeting c-kit, platelet-d | ||||
| 512193 | ITI-214(phosphate) | 1642303-38-5 | 98% Min. | ![]() |
| ITI-214 is a potent and selective phosphodiesterase 1 (PDE1) inhibitor. As the clinic | ||||
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