Abstract
Hydrazones are important classes of compounds found in many synthetic products. Due to their importance in synthetic chemistry, the present article reports the synthesis of twelve new hydrazone derivatives based on the coupling of 2,5-difluorobenzohydrazide with different benzaldehydes and screened for their antibacterial activities at the concentration 250 µg/mL with reference to the standard antibacterial drug Ampicillin. The screening results revealed that hydrazone derivatives 4d, 4e, 4f and 4h having fluorine substitution showed significant antibacterial activity comparable to that of standard drug Ampicillin.
Keywords: 2, 5-Difluoro benzoic acid, Aldehydes, Hydrazones, Antibacterial Activity, Fluorine, Gram positive.
Letters in Drug Design & Discovery
Title:Synthesis of Novel Hydrazone Derivatives of 2, 5-difluorobenzoic Acid as Potential Antibacterial Agents
Volume: 10 Issue: 7
Author(s): Rajasekhar Narisetty, K. B. Chandrasekhar, Sandeep Mohanty and B. Balram
Affiliation:
Keywords: 2, 5-Difluoro benzoic acid, Aldehydes, Hydrazones, Antibacterial Activity, Fluorine, Gram positive.
Abstract: Hydrazones are important classes of compounds found in many synthetic products. Due to their importance in synthetic chemistry, the present article reports the synthesis of twelve new hydrazone derivatives based on the coupling of 2,5-difluorobenzohydrazide with different benzaldehydes and screened for their antibacterial activities at the concentration 250 µg/mL with reference to the standard antibacterial drug Ampicillin. The screening results revealed that hydrazone derivatives 4d, 4e, 4f and 4h having fluorine substitution showed significant antibacterial activity comparable to that of standard drug Ampicillin.
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Narisetty Rajasekhar, Chandrasekhar B. K., Mohanty Sandeep and Balram B., Synthesis of Novel Hydrazone Derivatives of 2, 5-difluorobenzoic Acid as Potential Antibacterial Agents, Letters in Drug Design & Discovery 2013; 10 (7) . https://dx.doi.org/10.2174/1570180811310070009
DOI https://dx.doi.org/10.2174/1570180811310070009 |
Print ISSN 1570-1808 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-628X |
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