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苯并二噻嗪二氧化物的合成、抗肿瘤及抗HIV活性

Synthesis, antitumor and anti-HIV activities of benzodithiazine-dioxides.

作者信息

Brzozowski Zdziasław, Saczewski Franciszek, Neamati Nouri

机构信息

Department of Chemical Technology of Drugs, Medical University of Gdańsk, 80-416 Gdańsk, Poland.

出版信息

Bioorg Med Chem. 2006 May 1;14(9):2985-93. doi: 10.1016/j.bmc.2005.12.024. Epub 2006 Jan 6.

Abstract

Several 8-chloro-7-R1-6-R2-3-R3-imidazo[1,2-b][1,4,2]benzodithiazine 5,5-dioxide derivatives (9-11, 16-19, and 21-24) have been synthesized as potential antitumor or anti-HIV agents. The in vitro antitumor and anti-HIV-1 activities of the compounds were determined in a panel of cell lines. The benzodithiazine-dioxide 10 showed 50% growth inhibitory activity in low micromolar against most cells. It was particularly effective in leukemia, lung, melanoma, ovarian, and renal cancer cells with GI50 values of 1-2 microM. Interestingly, benzodithiazine-dioxide 16 showed remarkable anti-HIV-1 activity with 50% effective concentration EC50 value of 0.94 microM and no significant cytotoxicity at 200.0 microM.

摘要

已经合成了几种8-氯-7-R1-6-R2-3-R3-咪唑并[1,2-b][1,4,2]苯并二噻嗪5,5-二氧化物衍生物(9-11、16-19和21-24)作为潜在的抗肿瘤或抗HIV药物。在一组细胞系中测定了这些化合物的体外抗肿瘤和抗HIV-1活性。苯并二噻嗪二氧化物10在低微摩尔浓度下对大多数细胞显示出50%的生长抑制活性。它在白血病、肺癌、黑色素瘤、卵巢癌和肾癌细胞中特别有效,GI50值为1-2微摩尔。有趣的是,苯并二噻嗪二氧化物16显示出显著的抗HIV-1活性,50%有效浓度EC50值为0.94微摩尔,在200.0微摩尔时无明显细胞毒性。

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