Development of 2-arylbenzo[h]quinolone analogs as selective CYP1B1 inhibitors

作者：Dong, Jinyun; Wang, Zengtao; Meng, Qingqing; Zhang, Qijing; Huang, Guang; Cui, Jiahua^*; Li, Shaoshun^*

来源：RSC Advances, 2018, 8(27): 15009-15020.

DOI：10.1039/c8ra00465j

• BREAST-CANCER CELLS
• DOCETAXEL-RESISTANCE
• DRUG-RESISTANCE
• CYTOCHROME-P450
• EXPRESSION
• EFFICIENT
• ENZYMES
• 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN
• 17-BETA-ESTRADIOL
• DERIVATIVES

The CYP1B1 enzyme is regarded as a potential target for cancer prevention and therapy. Based on the structure of -naphthoflavone (ANF), diverse 2-arylbenzo[h]quinolone derivatives were designed, synthesized and evaluated as selective CYP1B1 inhibitors. Compared with ANF, although few of the title compounds possessed comparable or slightly higher CYP1B1 inhibitory activity, these compounds displayed a significantly increased selectivity toward CYP1B1 over CYP1A2. Among them compounds 5e, 5g and 5h potently inhibited the activity of CYP1B1 with IC50 values of 3.6, 3.9 and 4.1 nM respectively, paralleled by an excellent selectivity profile. On the basis of predicted clogP values, these target compounds may exhibit improved water-solubility compared to ANF. In particular, 5h showed a great superiority in the reversal of CYP1B1-mediated docetaxel resistance in vitro. The current study may serve as a good starting point for the further development of more potent as well as specific CYP1B1 inhibitors capable of reversing CYP1B1-mediated anticancer-drug resistance.

• 出版日期2018
• 单位上海交通大学