Design synthesis and biological evaluation of 2-methylphenyl semicarbazone derivatives
We have used pharmacophore hybridization technique of drug design and designed a pharmacophore model 2-methylphenylsemicarbazone which is having hydrogen acceptor site, hydrogen donor site, lipophilic site etc using ligandscout-2.02 software. A series of 2-methylphenyl-semicarbazone was synthesized...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Bangladesh Pharmacological Society,
2011-06-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | We have used pharmacophore hybridization technique of drug design and designed a pharmacophore model 2-methylphenylsemicarbazone which is having hydrogen acceptor site, hydrogen donor site, lipophilic site etc using ligandscout-2.02 software. A series of 2-methylphenyl-semicarbazone was synthesized and evaluated for their antipyretic activity using boiled cow milk induced pyrexia in rabbits. Compound 11 was the most active compound. The possible metabolites of some selected synthesized chalconesemicarbazones were predicted by computational method using Pallas version-3.1 ADME-Tox prediction software. The major pathway of metabolism was found to be p-hydroxylation and amide hydrolysis. |
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| Item Description: | 10.3329/bjp.v6i1.7771 1991-0088 |