GET THE APP

Synthesis, anti-microbial activity and docking study of cinnamic acid Esters of Salicylanides | Abstract

Der Pharma Chemica
Journal for Medicinal Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences and Computational Chemistry

ISSN: 0975-413X
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission Systemof respective journal.

Abstract

Synthesis, anti-microbial activity and docking study of cinnamic acid Esters of Salicylanides

Author(s): AP Rajput and Sonali A Patil

In recent days, spread of fungal, viral and microbial infections and their resistance to antibiotics compel us to develope new, powerful and effective pharmaceutics. Thus cinnamic acid esters of salicylanides are synthesized and evaluated for their antimicrobial activity in vitro. All the compounds are characterized by spectroscopic techniques such as FTIR, H1 NMR, C13 NMR and Mass. Molecular docking of these compounds is carried out in silico. Molecular docking of these compounds is carried out with enzyme β-Ketoacyl-acyl carrier protein synthase III from Escherichia coli (ecKAS III pdb id: 1HNJ) as a receptor responsible for growth of bacteria. The results showed that all Cinnamic acid esters of salicylanides are good inhibitors of β-Ketoacyl-acyl carrier protein synthase III.


PDF

Select your language of interest to view the total content in your interested language

30+ Million Readerbase
SCImago Journal & Country Rank
Google Scholar citation report
Citations : 25868

Der Pharma Chemica received 25868 citations as per Google Scholar report

Der Pharma Chemica peer review process verified at publons
Der Pharma Chemica- Journals on pharmaceutical chemistry