中山醫學大學機構典藏 CSMUIR:Item 310902500/23432
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    题名: Copper(I)-Catalyzed Nitrile-Addition/N-Arylation Ring-Closure Cascade: Synthesis of 5,11-Dihydro-6H-indolo[3,2-c]quinolin-6-ones as Potent Topoisomerase-I Inhibitors
    作者: Hsueh, WY;Lee, YSE;Huang, MS;Lai, CH;Gao, YS;Lin, JC;Chen, YF;Chang, CL;Chou, SY;Chen, SF;Lu, YY;Chang, LH;Lin, SF;Lin, YH;Hsu, PC;Wei, WY;Huang, YC;Kao, YF;Teng, LW;Liu, HH;Chen, YC;Yuan, TT;Chan, YW;Huang, PH;Chao, YT;Huang, SY;Jian, BH;Huang, HY;Yang, SC;Lo, TH;Huang, GR;Wang, SY;Lin, HS;Chuang, SH;Huang, JJ
    日期: 2021
    上传时间: 2022-08-05T09:37:13Z (UTC)
    出版者: AMER CHEMICAL SOC
    ISSN: 0022-2623
    摘要: In this paper, we present a copper(I)-catalyzed nitrile-addition/N-arylation ring-closure cascade for the synthesis of 5,11-dihydro-6H-indolo[3,2-c]quinolin-6-ones from 2-(2-bromophenyl)-N-(2-cyanophenyl)acetamides. Using CuBr and t-BuONa in dimethylformamide (DMF) as the optimal reaction conditions, the cascade reaction gave the target products, in high yields, with a good substrate scope. Application of the cascade reaction was demonstrated on the concise total syntheses of alkaloid isocryptolepine. Further optimization of the products from the cascade reaction led to 3-chloro-5,12-bis[2-(dimethylamino)ethyl]- 5,12-dihydro- 6H-[1,3]dioxolo[ 4',5':5,6]indolo[3,2-c]quinolin-6-one (2k), which exhibited the characteristic DNA topoisomerase-I inhibitory mechanism of action with potent in vitro anticancer activity. Compound 2k actively inhibited ARC-111- and SN-38-resistant HCT-116 cells and showed in vivo activity in mice bearing human HCT-116 and SJCRH30 xenografts. The interaction of 2k with the Top-DNA cleavable complex was revealed by docking simulations to guide the future optimization of 5,11-dihydro-6H-indolo[3,2-c]quinolin-6-ones as topoisomerase-I inhibitors.
    URI: http://dx.doi.org/10.1021/acs.jmedchem.0c00727
    https://www.webofscience.com/wos/woscc/full-record/WOS:000619743200008
    https://ir.csmu.edu.tw:8080/handle/310902500/23432
    關聯: JOURNAL OF MEDICINAL CHEMISTRY ,2021,v64,issue 3, P1435-1453
    显示于类别:[中山醫學大學研究成果] 期刊論文

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