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新型甾体查耳酮肟的合成及抗菌抗氧化研究。

Synthesis antimicrobial and antioxidant studies of new oximes of steroidal chalcones.

机构信息

Department of Chemistry, University of Kashmir, Srinagar 190009, J&K, India.

出版信息

Steroids. 2013 Sep;78(9):945-50. doi: 10.1016/j.steroids.2013.05.015. Epub 2013 Jun 5.

Abstract

A convenient synthesis of oximes of steroidal chalcones (4a-4j) was performed and structural assignment of the products was confirmed on the basis of IR, (1)HNMR, (13)C NMR, MS and analytical data. The synthesized compounds were screened for in vitro antioxidant activity by using DPPH method and in vitro antimicrobial activity against different bacterial and fungal strains by agar diffusion method. The activity of the tested compounds against each microbe varied due to structural differences between them. Presence and position of different substituents on the benzene ring of the chalconyl pendent had a marked effect on the activity of the compounds. From the results it can be inferred that the compounds 4a-j showed significant antioxidant activity and antimicrobial activity against all microbial strains used for testing.

摘要

方便地合成了甾体查尔酮的肟(4a-4j),并根据 IR、(1)HNMR、(13)C NMR、MS 和分析数据确定了产物的结构归属。通过 DPPH 法筛选了合成化合物的体外抗氧化活性,并通过琼脂扩散法筛选了它们对不同细菌和真菌菌株的体外抗菌活性。由于它们之间的结构差异,测试化合物对每种微生物的活性也有所不同。查尔酮侧链苯环上不同取代基的存在和位置对化合物的活性有显著影响。从结果可以推断,化合物 4a-j 对所有用于测试的微生物菌株均表现出显著的抗氧化和抗菌活性。

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