Synthesis of Schiffbases as potent sa-fab1 inhibitors and antibacterial agents

Kristỳna Labudová, Dhanya Sunil, Pooja R. Kamath

Research output: Contribution to journalArticle

Abstract

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 schiffbases and determination of its antibacterial potential. Molecular docking studies of schiffbase 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.

Original languageEnglish
Pages (from-to)493-498
Number of pages6
JournalDer Pharma Chemica
Volume8
Issue number2
Publication statusPublished - 01-01-2016

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Anti-Bacterial Agents
Pathogens
NADP
Oxidoreductases
Crystal structure
Molecules

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

Cite this

Labudová, Kristỳna ; Sunil, Dhanya ; Kamath, Pooja R. / Synthesis of Schiffbases as potent sa-fab1 inhibitors and antibacterial agents. In: Der Pharma Chemica. 2016 ; Vol. 8, No. 2. pp. 493-498.
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Synthesis of Schiffbases as potent sa-fab1 inhibitors and antibacterial agents. / Labudová, Kristỳna; Sunil, Dhanya; Kamath, Pooja R.

In: Der Pharma Chemica, Vol. 8, No. 2, 01.01.2016, p. 493-498.

Research output: Contribution to journalArticle

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