| Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
|---|---|---|---|---|
| 230403 | (R,S)-BI 1015550 | 1423719-27-0 | ≧98.0% | ![]() |
| BI 1015550 is a novel PDE4 inhibitor showing a preferential enzymatic inhibition of P | ||||
| 237072 | AZD0095 | 2750001-23-9 | ≧98.0% | ![]() |
| AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology. | ||||
| 20508 | AZD5991 | 2143061-81-6 | ≧98.0% | ![]() |
| AZD5991 is a potent and selective Mcl-1 inhibitor for treatment of hematologic cancer | ||||
| 20511 | PDD4091 | 1373651-41-2 | ≧98.0% | ![]() |
| PDD4091 is a novel G6PD inhibitor. | ||||
| 20512 | BDTX-1535 | 2607829-38-7 | ≧98.0% | ![]() |
| BDTX-1535 is a brain-penetrant and potent MasterKey inhibitor of oncogenic mutations | ||||
| 20514 | NMS-293 ( NMS-P293 ) | 1606996-12-6 | ≧98.0% | ![]() |
| NMS-293 is a PARP-1 inhibitor in early clinical development at Nerviano Medical Scien | ||||
| 20515 | 3-AMINO-3-(4-CHLOROPHENYL)PROPIONIC ACID | 19947-39-8 | 98% Min. | ![]() |
| 20516 | (S)-3-AMINO-3-(4-CHLORO-PHENYL)-PROPIONIC ACID | 131690-60-3 | 98% Min. | ![]() |
| 20517 | HM43239 | 2569527-64-4 | 98% Min. | ![]() |
| HM43239 is an orally active small molecule inhibitor of FLT3 that selectively inhibit | ||||
| 20518 | BMS-986141 | 1478711-48-6 | 98% Min. | ![]() |
| BMS-986141 is an Orally-Active Small-Molecule Antagonist of the Platelet Protease-Act | ||||
| 20519 | BMS-986120 | 1478712-37-6 | 98% Min. | ![]() |
| BMS-986120 is a potent and selective oral antagonist of protease-activated receptor-4 | ||||
| 20520 | 4,5-diiodo-2-methyl-triazole | 859790-39-9 | 98% Min. | ![]() |
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