کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1367379 | 981630 | 2006 | 4 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Search of antitubercular activities in tetrahydroacridines: Synthesis and biological evaluation Search of antitubercular activities in tetrahydroacridines: Synthesis and biological evaluation](/preview/png/1367379.png)
A series of 9-substituted tetrahydroacridines were synthesized by nucleophilic substitution of chloro group with different nucleophiles in 9-chlorotetrahydroacridine (2). The latter could be obtained by POCl3 mediated cyclization of the intermediate enamine, which in turn, was prepared by acid catalyzed condensation of anthranilic acid and cyclohexanone. Most of the compounds on antitubercular evaluation against M. tuberculosis H37 Rv and H37 Ra strains exhibited potent activities with MIC 6.125–0.78 μg/mL comparable to the standard drugs.
A series of 9-aminotetrahydroacridines were synthesized starting from anthranilic acid and cyclohexanone. Few of the compounds possess potent in vitro antitubercular activities with MIC as low as 0.78 μg/mL.Figure optionsDownload as PowerPoint slide
Journal: Bioorganic & Medicinal Chemistry Letters - Volume 16, Issue 19, 1 October 2006, Pages 5144–5147