SYNTHESIS OF 2, 4, 5- TRIPHENYL IMIDAZOLE DERIVATIVES AND BIOLOGICAL EVALUATION FOR THEIR ANTIBACTERIAL AND ANTI-INFLAMMATORY ACTIVITY
AbstractOn the basis of various literature survey, imidazole derivatives show various activity such as antimicrobial, anti-inflammatory, analgesic, antitubercular, anticancer etc. The possible improvements in the activity can be further achieved by slight modifications in the substituents on the basic imidazole nucleus. Having structural similarity with histidine imidazole compound can bind with protein molecules with ease compared to the some other heterocyclic moieties. Thus imidazole offers better pharmacodynamic characteristics. Furthermore, some imidazole drugs, at high concentrations, could exert direct inhibitory effects on membranes, without interference with sterols and sterol esters. Various recent new drugs developments in imidazole derivatives show better effect and less toxicity. Prompted by the broad spectrum activities of 2, 4, 5- triphenylimidazole derivatives, it was decided to synthesize various 2, 4, 5-triphenyl-1-substituted imidazoles and to evaluate them for their pharmacological activities.
Article Information
42
4051-4057
444KB
4227
English
IJPSR
Swati D. Burungale* and M. J. Bhitre
C. U. Shah College Of Pharmacy, S. N. D. T. Women’s University, Juhu, Santacruz (W), Mumbai- 400049, India
swati_sarak@yahoo.com
20 April, 2013
10 July, 2013
26 September, 2013
http://dx.doi.org/10.13040/IJPSR.0975-8232.4(10).4051-57
01 October, 2013
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