GET THE APP

Synthesis of Schiff bases as potent sa-fab1 inhibitors and antibacterial agents | 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 of Schiff bases as potent sa-fab1 inhibitors and antibacterial agents

Author(s): Kristýna Labudová, Dhanya Sunil* and Pooja R. Kamath

Staphylococus aureusis a ubiquitous pathogen responsible for broadspectrum of human infections. Treatment is very limited due to its resistence to current antibiotics and there is an urgent need to develop new antibiotics which will be more effective. This study focuses on synthesis and characterization of two new series of schiff bases and determination of its antibacterial potential.Molecular docking studies of schiff base molecules were carried out using enoyl-ACP reductase crystal structure complexed with NADPH.Compounds 3dand 6bthat showed high docking score in in silico studies exhibited good antibacterial properties against S. aureus. The higher antibacterial activity and better docking properties reflects the potential of 3d and 6b as potential leads for developing antibacterial agents aginst S aureus.


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 : 15261

Der Pharma Chemica received 15261 citations as per Google Scholar report

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