新型 1,3,4-恶二唑衍生物的药理评估

Aswathy Ramesh, R. Jat, R. Arunkumar
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引用次数: 0

摘要

水杨酸和苯乙酸与各种芳香酸在氧氯化磷作为环化剂存在下发生环缩合反应,然后进行重排,合成了一系列 2,5-二取代-1,3,4-噁二唑衍生物(Ox1-Ox10)。新衍生物的结构通过光谱分析得到了证实。对 PASS 软件中 Pa 值较高的衍生物进行了抗菌、抗癌和抗糖尿病研究,结果令人鼓舞。这项研究有助于并激励研究人员利用噁二唑核来开发活性更强、危害更小的药物:1,3,4-噁二唑;抗菌活性;抗癌活性;抗糖尿病活性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological Evaluation of Novel 1,3,4-Oxadiazole Derivatives
A series of 2, 5- disubstituted- 1, 3, 4-oxadiazole derivatives (Ox1-Ox10) are synthesized by the ring condensation reaction followed by rearrangement of salicylic acid and phenyl acetic acid with various aromatic acids in presence of phosphorous oxychloride as cyclizing agent. Structure of the new derivatives are confirmed by spectral analysis. Those derivatives having high Pa value in PASS software are subjected to antibacterial, anticancer and antidiabetic studies which yield promising reports. This study helps and stimulate the researcher to exploit the oxadiazole nuclei for the development of more active less harmful drugs. Keywords: 1,3,4-oxadiazole, antibacterial activity, anticancer activity, antidiabetic activity
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