Literature DB >> 18843413

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

Namdev S Vatmurge1, Braja G Hazra, Vandana S Pore, Fazal Shirazi, Mukund V Deshpande, Sreenath Kadreppa, Samit Chattopadhyay, Rajesh G Gonnade.   

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.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18843413     DOI: 10.1039/b809221d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Design, synthesis, anticancer activity and docking studies of theophylline containing 1,2,3-triazoles with variant amide derivatives.

Authors:  Radhakrishnam Raju Ruddarraju; Adharvana Chari Murugulla; Ravindar Kotla; Muni Chandra Babu Tirumalasetty; Rajendra Wudayagiri; Shobha Donthabakthuni; Ravichandar Maroju
Journal:  Medchemcomm       Date:  2016-10-28       Impact factor: 3.597

2.  Shortcut access to peptidosteroid conjugates: building blocks for solid-phase bile acid scaffold decoration by convergent ligation.

Authors:  Dieter Verzele; Sara Figaroli; Annemieke Madder
Journal:  Molecules       Date:  2011-12-07       Impact factor: 4.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.