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BMS-202

维基百科,自由的百科全书
BMS-202
临床资料
ATC码
  • 未分配
法律规范状态
法律规范
  • Investigational
识别信息
  • N-(2-(((2-methoxy-6-((2-methyl-[1,1'-biphenyl]-3-yl)methoxy)pyridin-3-yl)methyl)amino)ethyl)acetamide
CAS号1675203-84-5  checkY
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英语JSmol
  • CC1=C(C=CC=C1C2=CC=CC=C2)COC3=NC(=C(C=C3)CNCCNC(=O)C)OC
  • InChI=1S/C25H29N3O3/c1-18-22(10-7-11-23(18)20-8-5-4-6-9-20)17-31-24-13-12-21(25(28-24)30-3)16-26-14-15-27-19(2)29/h4-13,26H,14-17H2,1-3H3,(H,27,29)
  • Key:JEDPSOYOYVELLZ-UHFFFAOYSA-N

BMS-202是一种含氮有机化合物,分子式C
25
H
29
N
3
O
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]
  1. ^ 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可免费查阅. PMID 36169254. doi:10.1002/iid3.693. 
  2. ^ 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可免费查阅.