BMS-202
外观
| 临床资料 | |
|---|---|
| ATC码 |
|
| 法律规范状态 | |
| 法律规范 |
|
| 识别信息 | |
| |
| CAS号 | 1675203-84-5 |
| PubChem CID | |
| IUPHAR/BPS | |
| ChemSpider | |
| UNII | |
| ChEMBL | |
| 化学信息 | |
| 化学式 | C25H29N3O3 |
| 摩尔质量 | 419.53 g·mol−1 |
| 3D模型(JSmol) | |
| |
| |
BMS-202是一种含氮有机化合物,分子式C
25H
29N
3O
3,为百时美施贵宝研发的小分子PD-1/PD-L1抑制剂,用于治疗胶质母细胞瘤(GBM)[1][2]。
参考文献
[编辑]- ^ Cai Y, Xiao M, Li X, Zhou S, Sun Y, Yu W, Zhao T. BMS-202, a PD-1/PD-L1 inhibitor, decelerates the pro‑fibrotic effects of fibroblasts derived from scar tissues via ERK and TGFβ1/Smad signaling pathways. Immunity, Inflammation and Disease. 2022, 10 (10): e693. PMC 9449589
. PMID 36169254. doi:10.1002/iid3.693.
- ^ Ashizawa T, Iizuka A, Tanaka E, Kondou R, Miyata H, Maeda C, Sugino T, Yamaguchi K, Ando T, Ishikawa Y, Ito M, Akiyama Y. Antitumor activity of the PD-1/PD-L1 binding inhibitor BMS-202 in the humanized MHC-double knockout NOG mouse. Biomedical Research. 2019, 40 (6): 243–250. PMID 31839668. doi:10.2220/biomedres.40.243
.