溶解性 | DMSO |
存贮条件 | 储存温度-20°C |
产品介绍 | (R)-(-)-JQ1 Enantiomer是(+)-JQ1的立体异构体,与布罗莫结构域无显著的相互作用。而(+)-JQ1则是BET抑制剂。 |
生化机理 | (±)-JQ1 displaces BET proteins from chromatin by competitively binding to the acetyl-lysine recognition pocket of BET bromodomains. The (-)-JQ1 stereoisomer has no appreciable affinity to BET bromodomains, whereas enantiomerically pure (+)-JQ1 binds to BRD4 bromodomains 1 and 2 with Kd values of ~ 50 and 90 nM, respectively. |
别名 | (R)-(-)2-(4-(4-氯苯基)-2,3,9-三甲基-6H-噻吩并(3,2-f)(1,2,4)三唑并(4,3-a)(1,4)二氮杂环庚烷-6-基)乙酸叔丁酯;;(R)-(-)-JQ1 Enantiomer;(r)-(-)-tert-butyl 2-(4-(4-chlorophenyl)-2,3,9-trimethyl-6h-thieno(3,2-f)(1,2,4)triazolo(4,3-a)(1,4)diazepin-6-yl)acetate |