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3D-QSAR CoMFA studies on sulfonamide inhibitors of the Rv3588c β-carbonic anhydrase from Mycobacterium tuberculosis and design of not yet synthesized new molecules

机译：3D-QSAR COMFA研究RV358Cβ-碳酸酐酶的磺胺酰胺抑制剂免于三分枝杆菌的结核分枝杆菌和尚未合成的新分子设计

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Shalini Singh; Claudiu T. Supuran;
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1. 3D-QSAR CoMFA studies on sulfonamide inhibitors of the Rv3588c beta-carbonic anhydrase from Mycobacterium tuberculosis and design of not yet synthesized new molecules [J] . Singh Shalini, Supuran Claudiu T. Journal of enzyme inhibition and medicinal chemistry. . 2014,第1a6期

机译：3D-QSAR CoMFA对来自结核分枝杆菌的Rv3588cβ-碳酸酐酶的磺酰胺抑制剂的研究以及尚未合成的新分子的设计
2. 3D-QSAR CoMFA studies on sulfonamide inhibitors of the Rv3588c β-carbonic anhydrase from Mycobacterium tuberculosis and design of not yet synthesized new molecules [J] . Shalini Singh, Claudiu T. Supuran Journal of enzyme inhibition and medicinal chemistry. . 2014,第3期

机译：3D-QSAR CoMFA研究结核分枝杆菌Rv3588cβ-碳酸酐酶的磺酰胺抑制剂和尚未合成的新分子的设计
3. 3D-QSAR CoMFA studies on sulfonamide inhibitors of the Rv3588c β-carbonic anhydrase from Mycobacterium tuberculosis and design of not yet synthesized new molecules [J] . Shalini Singh, Claudiu T. Supuran Journal of enzyme inhibition and medicinal chemistry. . 2014,第3期

机译：3D-QSAR CoMFA研究结核分枝杆菌Rv3588cβ-碳酸酐酶的磺酰胺抑制剂和尚未合成的新分子的设计
4. 3D-QSAR and 3D-QSSR studies on a series of HDAC2 inhibitors using Topomer CoMFA [C] . Hou Zhaoyan, Xiang Yuhong, Wei Yanbo, 2011 4th International Conference on Biomedical Engineering and Informatics . 2011

机译：使用Topomer CoMFA对一系列HDAC2抑制剂进行3D-QSAR和3D-QSSR研究
5. I. Structure-based molecular modeling and synthesis of indole derivatives as non-phenolic analogues of mycophenolic acid. II. 3D-QSAR studies using CoMFA on homotropane and tropane derivatives as dopamine transporter and serotonin transporter ligands. [D] . El-Araby, Moustafa El-Sayed. 2001

机译：I.基于结构的分子模型和吲哚衍生物作为霉酚酸的非酚类似物的合成。二。 3D-QSAR研究使用CoMFA对高碘烷和托烷衍生物作为多巴胺转运蛋白和5-羟色胺转运蛋白配体的研究。
6. Dichloro-naphthoquinone as a non-classical inhibitor of the mycobacterial carbonic anhydrase Rv3588c [O] . M. A. Dallaston, S. Rajan, J. Chekaiban, 1924

机译：二氯萘醌作为分枝杆菌碳酸酐酶Rv3588c的非经典抑制剂
7. Carbonic Anhydrase Inhibitors. Part 551 Metal Complexes of 1,3,4-Thiadiazole-2-Sulfonamide Derivatives: In Vitro Inhibition Studies With Carbonic Anhydrase Isozymes I, II and IV [O] . Supuran, Claudiu T., Scozzafava, Andrea, Briganti, Fabrizio, 1998

机译：碳酸酐酶抑制剂。 551部分的1,3,4-噻二唑-2-磺酰胺衍生物的金属配合物：体外抑制碳酸酐酶同工酶I，II和IV的研究

3D-QSAR CoMFA studies on sulfonamide inhibitors of the Rv3588c β-carbonic anhydrase from Mycobacterium tuberculosis and design of not yet synthesized new molecules

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