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首页> 外文期刊>Asian journal of research in chemistry >Synthesis and Biological Activities of Novel Thieno [3,2-d] Pyrimidine Derivatives
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Synthesis and Biological Activities of Novel Thieno [3,2-d] Pyrimidine Derivatives

机译:新型噻吩的合成与生物活性[3,2-D]嘧啶衍生物

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摘要

A series of novel 4-Substituted/Heterocyclic-N-(4-thiomorpholinothieno[3,2-d]pyrimidin-2-yl)benzamide (8a-j)derivatives were synthesized by a Five-step procedure that afforded advantages of mild reaction conditions, simple protocol and good yields. The structures of the final compounds were confirmed by IR, NMR, EI-MS. The final compounds were screened for their anti-bacterial activity against Staphylococcus aureus (S. aureus) and Bacillus subtilis (B. subtilis)from Gram positive group of bacteria and Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli)from Gram negative group of bacteria and antifungal activity against Aspergillus niger (A. niger) and Candida albicans (C. albicans). Anti-bacterial and anti-fungal activities were Evaluated and compared with the standard drugs Such as Amoxicillin and Flucanazole From anti-bacterial and anti-fungal activity screening results, it has been observed that compounds 8j, 8i, 8e and 8fpossess good activity.
机译:通过一项提供温和反应的优点,合成了一系列新的4取代/杂环-2-(4-硫胺啉噻吩[3,2-D]嘧啶-2-基-2-基)苯甲酰胺(8A-J)衍生物。 条件,简单的协议和良好的产量。 通过IR,NMR,EI-MS确认最终化合物的结构。 将最终化合物筛选抗细菌活性,抵抗葡萄球菌的金黄色葡萄球菌(金黄色葡萄球菌)和枯草芽孢杆菌(B.枯草芽孢杆菌),来自细菌和铜绿假单胞菌(P. Aeruginosa)和大肠杆菌(大肠杆菌)的克阳性组 针对曲霉和抗原活性的克原群和抗真菌活性群(A. niger)和念珠菌类肽(念珠菌类白葡萄酒)。 评估抗细菌和抗真菌活性,并与抗细菌和抗真菌活性筛查结果的标准药物如阿莫西林和氟氯吡喃唑如抗菌药物,并且已经观察到化合物8J,8I,8E和8FPossess良好活性。

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