Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21650
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dc.contributor.authorRani, Preeti-
dc.contributor.authorSrivastava, V K-
dc.contributor.authorKurnar, Ashok-
dc.date.accessioned2013-10-07T10:14:37Z-
dc.date.available2013-10-07T10:14:37Z-
dc.date.issued2003-07-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21650-
dc.description1729-1733en_US
dc.description.abstractA number of 5-substituted-N-[4'-(substitutedphenyl)aminomethyl-5' (substitutedphenyl)isoxazolin-2'-yl]anthranilic acids have been synthesized by the Mannich reaction of 5-substituted-N-[5'-(substitutedphenyl)isoxazolin-2'-y l]anthranilic acids, which in turn is synthesized by the reaction of 5-substituted-N-chalconylanthranilic acids. In this series, compounds 9,11, 15 and 18 show significant protection against carrageenan induced rat's paw oedema with lower ulcerogenic liability than phenylbutazone. The most active compound of this series is N-[5'-(m-methoxy, p-hydroxyphenyl)isoxazolin-2'yl] anthranilic acid which has shown higher antiinflammatory activity and lower ulcerogenic property than phenylbutazone.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(07) [July 2003]en_US
dc.titleIsoxazolinyl derivatives of anthranilic acid as antiinflammatory agentsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(07) [July 2003]

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