编号 | 化学名称 | Cas号 | 纯度 | 化学结构 |
---|---|---|---|---|
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% | |
AZD-5991 是一种有效的选择性 Mcl-1 抑制剂。 | ||||
20511 | PDD4091 | 1373651-41-2 | ≧98.0% | |
PDD4091 是一种新颖的G6PD抑制剂。 | ||||
20512 | BDTX-1535 | 2607829-38-7 | ≧98.0% | |
BDTX-1535 是一种突变选择性、不可逆的第四代 EGFR 抑制剂。 | ||||
20514 | NMS-293 ( NMS-P293 ) | 1606996-12-6 | ≧98.0% | |
NMS-293 是 Nerviano Medical Sciences 处于早期临床开发阶段的 PARP-1 抑制 | ||||
20515 | 3-氨基-3-(4-氯苯基)丙酸 | 19947-39-8 | 98% Min. | |
20516 | (S)-3-氨基-3-(4-氯苯基)-丙酸 | 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 | 4,5-二碘-2-甲基-1,2,3三氮唑 | 859790-39-9 | 98% Min. | |
20521 | 4,5-二碘-1H-1H-1,2,3-三氮唑 | 28194-09-4 | 98% Min. | |