Please use this identifier to cite or link to this item:
http://10.1.7.192:80/jspui/handle/123456789/2535
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chhabria, Mahesh T. | - |
dc.contributor.author | Bhatt, Hardik G. | - |
dc.contributor.author | Raval, Hitesh G. | - |
dc.contributor.author | Oza, Pratik M. | - |
dc.date.accessioned | 2011-07-22T05:18:05Z | - |
dc.date.available | 2011-07-22T05:18:05Z | - |
dc.date.issued | 2007 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2535 | - |
dc.description | Bioorganic & Medicinal Chemistry Letters 17 (2007) 1022–1024 | en_US |
dc.description.abstract | Synthesis and biological evaluation of some 5-ethoxycarbonyl-6-isopropylamino-4-(substitutedphenyl)aminopyrimidines have been achieved by cyclization of N-[2-ethoxycarbonyl-2-cyano-1-(isopropylamino)vinyl] formamidine in presence of dry HCl in dioxane followed by nucleophilic substitution of 4-chloro group with substituted aromatic amine or phenoxide. Target compounds were evaluated for their analgesic and anti-inflammatory potential by known experimental models. Some of the compounds emerged out as more potent than standard drugs. Very low ulcer index was observed for the potent compounds.2006 Elsevier Ltd. All rights reserved. | en_US |
dc.publisher | Elsevier Publication | en_US |
dc.relation.ispartofseries | IPFP0022 | en_US |
dc.subject | Aminopyrimidines | en_US |
dc.subject | Analgesic | en_US |
dc.subject | Anti-inflammatory | en_US |
dc.subject | Cyclooxygenase | en_US |
dc.subject | NSAIDs | en_US |
dc.subject | Facuty Paper | en_US |
dc.subject | Pharmacy Faculty Paper | en_US |
dc.subject | IPFP0022 | en_US |
dc.title | Synthesis and biological evaluation of some 5-ethoxycarbonyl-6- isopropylamino-4-(substitutedphenyl)aminopyrimidines as potent analgesic and anti-inflammatory agents | en_US |
dc.type | Faculty Papers | en_US |
Appears in Collections: | Faculty Papers |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
IPFP0022.pdf | IPFP0022 | 116.77 kB | Adobe PDF | ![]() View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.