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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Microwave-assisted synthesis of N-substituted cyclic imides and their evaluation for anticancer and anti-inflammatory activities.
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Microwave-assisted synthesis of N-substituted cyclic imides and their evaluation for anticancer and anti-inflammatory activities.

机译:微波辅助合成N-取代的环酰亚胺及其抗癌和抗炎活性的评估。

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摘要

A number of N-substituted cyclic imides 3a-e, 5a-e, 7a-d, and 9a-e have been synthesized in very high yields, by condensation of various diacids 2, 4, 6, and 8 with different amines under microwave irradiation. These compounds were screened for anticancer and anti-inflammatory activities, and compounds 3c, 3e, 5c, 9c, and 9d exhibited anticancer activity against colon (COLO 205) cancer better than 5-fluorouracil and mitomycin-C, and compound 9b exhibited anti-inflammatory activity better than standard drug phenyl butazone.
机译:通过在微波下将各种二酸2、4、6和8与不同的胺缩合,以很高的收率合成了许多N-取代的环状酰亚胺3a-e,5a-e,7a-d和9a-e。辐射。筛选了这些化合物的抗癌和抗炎活性,化合物3c,3e,5c,9c和9d对结肠癌(COLO 205)的抗癌活性优于5-氟尿嘧啶和丝裂霉素C,而化合物9b对5-炎症活性优于标准药物苯基丁but。

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