药用苯并噻唑缩合氧咔唑和氧杂氮咔唑的二氮卓类和喹啉类羧酸取代类似物合成新可能性的探索

V. Soni, Meenakshi Sharma, Vaishali Soni, S. Soni
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引用次数: 0

摘要

含有苯并噻唑、咔唑(和氮杂咔唑)基团的杂环体系引起了化学家的注意,因为这些核在文献中被认为是药物设计和合成中最有前途的药效团。基于这些观察结果,可以预见,在与咔唑(和氮杂咔唑)融合的苯并噻唑分子框架中加入具有生物活性的氮卓和喹啉部分,可以产生一系列具有增强生物活性的有趣化合物9-12,其结构从其微观分析和光谱数据中得到明确的确定。
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Exploration of Newer Possibilities to the Synthesis of Diazepine and Quinoline Carboxylic Acid Substituted Analogues of Benzothiazolo Condensed Oxocarbazoles and Oxoazacarbazoles of Medicinal Interest
Heterocyclic systems containing benzothiazoles, carbazole (and azacarbazole) moieties have attracted the attention of chemists owing to these nuclei having been identified in the literature as most promising pharmacophores in drug design and synthesis. Based on these observations, it could be anticipated that incorporation of the bioactive azepine moiety and quinoline moiety into the molecular framework of benzothiazoles fused to carbazole (and azacarbazoles) could produce interesting series of compounds 9-12 with enhanced biological activities, whose structure was unequivocally established from its micro analyses and spectral data.
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