Design, synthesis, characterization, and antibacterial activity of 5-chloro-2-(3-substitutedphenyl-1,2,4-oxadiazol-5-yl)-methoxy-phenyl-(phenyl)-methanones

Rai, Neithnadka Premsai and Narayanaswamy, V. K. and Govender, Thavendran and Manuprasad, B. K. and Shashikanth, Sheena and Arunachalam, Pirama Nayagam (2010) Design, synthesis, characterization, and antibacterial activity of 5-chloro-2-(3-substitutedphenyl-1,2,4-oxadiazol-5-yl)-methoxy-phenyl-(phenyl)-methanones. European Journal of Medicinal Chemistry, 45 (6). 2677 - 2682. ISSN 1768-3254

[img] Text (Full Text)
Design synthesis characterization.pdf - Published Version
Restricted to Registered users only

Download (224kB) | Request a copy
Official URL: http://www.sciencedirect.com/science/article/pii/S...

Abstract

In the present investigation, a series of novel 5-chloro-2-(3-(substitutedphenyl)-1,2,4-oxadiazol-5-yl)-methoxy-phenyl-(phenyl)-methanones (3a–i) have been synthesized from 5-(chloromethyl)-3-substitutedphenyl-1,2,4-oxadiazole (2a–i). The newly synthesized compounds were characterized by IR, NMR (1H and 13C), mass spectral and elemental analysis. The title compounds were investigated for in-vitro qualitative (zone of inhibition) and quantitative (MIC) antibacterial activity by agar cup plate and microtitration methods, respectively. The minimum inhibitory concentration and structure activity relationships (SARs) were evaluated. Amongst the synthesized compounds in this series, 5-chloro-2-(3-(2,5-difluoro-4-methyl-phenyl)-1,2,4-oxadiazol-5-yl)-methoxy-phenyl-(phenyl)-methanone (3d) was found to exhibit significant activity with MICs of 21.5, 22.4, 29.8 and 30.6μg/mL against Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae, respectively.

Item Type: Article
Uncontrolled Keywords: 1,2,4-Oxadiazoles, Substituted methanones, Antibacterial activity
Subjects: C Chemical Science > Chemistry
Divisions: Department of > Chemistry
Depositing User: LA manjunath user
Date Deposited: 12 Jul 2019 05:29
Last Modified: 22 Dec 2020 07:06
URI: http://eprints.uni-mysore.ac.in/id/eprint/5106

Actions (login required)

View Item View Item