Design, synthesis and docking studies of some novel isocoumarin analogues as antimicrobial agents-Reference-Cited by-同舟云学术

Design, synthesis and docking studies of some novel isocoumarin analogues as antimicrobial agents

Published:2014 Issue:96 Volume:4 Page:53842-53853
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Ashraf Zaman¹²³⁴⁵,Saeed Aamer¹⁶⁷,Nadeem Humaira⁸⁹¹⁰

Affiliation:

1. Department of Chemistry

2. Allama Iqbal Open University

3. Islamabad 44000, Pakistan

4. Department of Biology

5. College of Natural Sciences

6. Quaid-I-Azam University

7. Islamabad 45320, Pakistan

8. Riphah Institute of Pharmaceutical Sciences

9. Riphah International University

10. Islamabad, Pakistan

Abstract

The isocoumarins have been designed and prepared by incorporating the NSAIDs to discover potential inhibitors of UDP-N-acetylmuramyl-l-alanine ligase (MurC).

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA07223E

Reference20 articles.

1. Bioactive Isocoumarins Isolated from the Endophytic Fungus Microdochium bolleyi

2. Structure–antimicrobial activity of some natural isocoumarins and their analogues

3. Intestinal Anti-Inflammatory Activity of Paepalantine, an Isocoumarin Isolated from the Capitula ofPaepalanthus bromelioides, in the Trinitrobenzenesulphonic Acid Model of Rat Colitis

4. Metabolites from Fungi 15. New Isocoumarins from an Endophytic Fungus Isolated from the Canadian ThistleCirsium arvense

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