[go: up one dir, main page]
Jump to content

BMS-202

Add links
From Wikipedia, the free encyclopedia

BMS-202
Clinical data
ATC code
  • none
Legal status
Legal status
  • Investigational
Identifiers
  • N-(2-(((2-methoxy-6-((2-methyl-[1,1'-biphenyl]-3-yl)methoxy)pyridin-3-yl)methyl)amino)ethyl)acetamide
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC25H29N3O3
Molar mass419.525 g·mol−1
3D model (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 is a small-molecule drug PD-L1 inhibitor developed by Bristol-Myers Squibb which displays significant anti-tumor activity against glioblastoma (GBM) cells.[1]In addition, BMS-202 has an inhibitory effect on both PD-L1-expressing cancer cells and activated T cells.[2]


References

[edit]
  1. ^ Cai Y, Xiao M, Li X, Zhou S, Sun Y, Yu W, Zhao T (2022). "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. 10 (10): e693. doi:10.1002/iid3.693. PMC 9449589. PMID 36169254.
  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 (2019). "Antitumor activity of the PD-1/PD-L1 binding inhibitor BMS-202 in the humanized MHC-double knockout NOG mouse". Biomedical Research. 40 (6): 243–250. doi:10.2220/biomedres.40.243. PMID 31839668.
Retrieved from "https://en.wikipedia.org/w/index.php?title=BMS-202&oldid=1255805933"