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与1,2,3-三唑和双β-内酰胺连接的胆汁酸二聚体的合成及生物学评价

Synthesis and biological evaluation of bile acid dimers linked with 1,2,3-triazole and bis-beta-lactam.

作者信息

Vatmurge Namdev S, Hazra Braja G, Pore Vandana S, Shirazi Fazal, Deshpande Mukund V, Kadreppa Sreenath, Chattopadhyay Samit, Gonnade Rajesh G

机构信息

Division of Organic Chemistry, National Chemical Laboratory, Pune, 411008, India.

出版信息

Org Biomol Chem. 2008 Oct 21;6(20):3823-30. doi: 10.1039/b809221d. Epub 2008 Aug 29.

Abstract

We report herein the synthesis and biological evaluation of bile acid dimers linked through 1,2,3-triazole and bis-beta-lactam. The dimers were synthesized using 1,3-dipolar cycloaddition reaction of diazido bis-beta-lactams , and terminal alkynes derived from cholic acid/deoxycholic acid in the presence of Cu(i) catalyst (click chemistry). These novel molecules were evaluated in vitro for their antifungal and antibacterial activity. Most of the compounds exhibited significant antifungal as well as antibacterial activity against all the tested fungal and bacterial strains. Moreover, their in vitro cytotoxicities towards HEK-293 and MCF-7 cells were also established.

摘要

我们在此报告通过1,2,3-三唑和双β-内酰胺连接的胆汁酸二聚体的合成及生物学评价。二聚体是在铜(I)催化剂存在下,利用重氮基双β-内酰胺与源自胆酸/脱氧胆酸的末端炔烃进行1,3-偶极环加成反应合成的(点击化学)。对这些新型分子进行了体外抗真菌和抗菌活性评估。大多数化合物对所有测试的真菌和细菌菌株均表现出显著的抗真菌和抗菌活性。此外,还测定了它们对HEK-293和MCF-7细胞的体外细胞毒性。

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