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Formula | C25H29N3O3 |
Molar mass | 419.525 g·mol |
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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.In addition, BMS-202 has an inhibitory effect on both PD-L1-expressing cancer cells and activated T cells.
References
- 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.
- 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.
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PD-1 inhibitorsTooltip Programmed cell death protein 1 | |
PD-L1 inhibitorsTooltip Programmed death-ligand 1 |