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首页> 外文期刊>Indian journal of pharmaceutical sciences. >AntiHIV, Antibacterial and Antifungal Activities of Some Novel 1,4-disubstituted-1,2,4-triazolo[4,3-a] quinazolin-5(4H)-ones
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AntiHIV, Antibacterial and Antifungal Activities of Some Novel 1,4-disubstituted-1,2,4-triazolo[4,3-a] quinazolin-5(4H)-ones

机译:某些新型1,4-二取代-1,2,4-三唑[4,3-a]喹唑啉5(4H)-one的抗HIV,抗菌和抗真菌活性

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The title compounds l-substimted-4-phenyl-l,2,4-triazolo[4,3-a]quinazolm-5(4H)-ones were synthesized by the cyclization of 2-hydrazino-3-phenylquinazolin-4(3H)-one with various one carbon donors. The starting material 2-hydxazino-3-phenylquinazolin-4(3H)-one was synthesized from aniline. Investigation of antimicrobial activity of the test compounds was made by agar cup-plate method against 8 pathogenic bacteria including Mycobacterium tuberculosis, 3 pathogenic fungi and antiHIV activity against replication of HIV-l(IIIB) and HIV-2(ROD) in MT-4 cells. The compound 7e inhibited 21% growth of M. tuberculosis at 6.25 ug/ml concentration, while the compounds 7c and 7d showed good antifungal activity against Candida albicans; and the compounds 7c exhibited good antifungal activity against Aspergillus niger.
机译:通过2-肼基-3-苯基喹唑啉-4(3H)的环化反应合成标题化合物l-亚甲基-4-苯基-1,2,4-三唑并[4,3-a]喹唑啉-5(4H)-。 )-具有多个碳供体的一个。由苯胺合成起始原料2-hydxazino-3-phenylquinazolin-4(3H)-one。用琼脂杯板法对受试化合物对包括结核分枝杆菌在内的8种病原菌,3种病原真菌和对HIV-4中HIV-1(IIIB)和HIV-2(ROD)的复制的抗HIV活性的抗微生物活性进行了研究。细胞。化合物7e在6.25 ug / ml的浓度下可抑制21%的结核分枝杆菌生长,而化合物7c和7d对白色念珠菌具有良好的抗真菌活性。化合物7c对黑曲霉表现出良好的抗真菌活性。

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