所有图片(1)
别名:
2,2’-Dimethyl-3,3’-bis[2-methoxy-3-(2-acetamidoethylamino)-methylpyridin-6-yl-oxymethyl]-1,1’-biphenyl, LH 1306, LH-1306, N,N′-(2,2′-(6,6′-(2,2′-Dimethylbiphenyl-3,3′-diyl)bis(methylene)bis(oxy)bis(2-methoxypyridine-6,3-diyl))bis(methylene)bis(azanediyl)bis(ethane-2,1-diyl))diacetamide
经验公式（希尔记法）:
C38H48N6O6
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生化/生理作用
LH1306 is a potent programmed cell death-1/programmed death-ligand 1 (PD-1 (CD279, PDCD1)/PD-L1 (B7-H1, PDCD1-L1)) protein-protein interaction (PPI) inhibitor (IC50 = 25 nM by HTRF assay) that induces symmetrically arranged PD-L1 homodimer formation by targeting PD-L1 at the PD-1 binding site. LH1306 effectively blocks cell surface PD-1/PD-L1 interaction between PD-1-expressing Jurkat cells and co-cultured PD-L1-expressing U2OS cells (SHP-1 recruitment IC50 = 334 nM) or co-cultured PD-L1-expressing aAPC/CHO-K1 cells (NFAT signaling restoration EC50 = 4.21 μM).
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
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