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Letters in Drug Design & Discovery

Editor-in-Chief

ISSN (Print): 1570-1808
ISSN (Online): 1875-628X

Synthesis and Biological Evaluation of Coumarin Linked Fluoroquinolones, Phthalimides and Naphthalimides as Potential DNA Gyrase Inhibitors

Author(s): A. Kamal, M. Satyanarayana, V. Devaiah, V. Rohini, J. S. Yadav, B. Mullick and V. Nagaraja

Volume 3, Issue 7, 2006

Page: [494 - 502] Pages: 9

DOI: 10.2174/157018006778194862

Price: $65

Abstract

A hybrid molecule synthesis strategy is employed to develop new molecules with potential antibacterial activity. Three types of coumarin-linked hybrids have been synthesized. The coumarin ring system has been linked to phthalimido, naphthalimido and quinolone moieties at 4-position through piperazino alkane spacers. These compounds have been evaluated for their antibacterial activity. Some of these new hybrids particularly phthalimido and naphthalimido ones have exhibited DNA gyrase inhibition activity.

Keywords: Coumarins, Phthalimides, Naphthalimides and Fluoroquinolone DNA gyrase inhibition


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