英文同义词:
TBOPP;2(1H)-Pyridinone, 1-[2-oxo-2-[3-(trifluoromethyl)[1,1-biphenyl]-4-yl]ethyl]-5-(1-pyrrolidinylsulfonyl)-;1-(2-Oxo-2-(3-(trifluoromethyl)-[1,1-biphenyl]-4-yl)ethyl)-5-(pyrrolidin-1-ylsulfonyl)pyridin-2(1H)-one
沸点
645.4±65.0 °C(Predicted)
密度
1.46±0.1 g/cm3(Predicted)
酸度系数(pKa)
-2.46±0.70(Predicted)
生物活性
TBOPP 是一种 dedicator of cytokinesis (DOCK1, Dock180) 的选择性抑制剂,可抑制DOCK1介导的Rac激活,IC50值为8.4 μM。TBOPP 可结合DOCK1 DHR-2结构域对应的Kd值为7.1 μM。TBOPP 表现出抗肿瘤的活性。
靶点
Target Value
DOCK1 DHR-2 domain
(Cell-free assay) 7.1 μM(Kd)
DOCK1-mediated Rac activation
(Cell-free assay) 8.4 μM
DOCK1 DHR-2 domain
(Cell-free assay)
7.1 μM(Kd)
DOCK1-mediated Rac activation
(Cell-free assay)
8.4 μM