Combinatorial synthesis and biological evaluation of isoxazole-based libraries as antithrombotic agents

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dc.contributor.author Batra, Sanjay
dc.contributor.author Srinivasan, T
dc.contributor.author Rastogi, S K
dc.contributor.author Kundu, Bijoy
dc.contributor.author Patra, A
dc.contributor.author Bhaduri, A P
dc.contributor.author Dikshit, Madhu
dc.date.accessioned 2008-01-17T11:16:20Z
dc.date.available 2008-01-17T11:16:20Z
dc.date.issued 2002
dc.identifier.citation Bioorg. Med. Chem. Lett. 12, 1905-1908, Bioorganic & Medicinal Chemistry Letters 12 (2002) 3349 en
dc.identifier.uri http://hdl.handle.net/123456789/80
dc.description.abstract The 3-substitutedphenyl-5-isoxazolecarboxaldehydes have been identified as activated aldehydes for the generation of isoxazole-based combinatorial libraries on solid phase through automation. Three highly functionalized isoxazole-based libraries comprising of 32, 96 and 45 compounds each have been synthesized in parallel format using Baylis Hillman reaction, Michael addition, reductive amination and alkylation reactions. With an objective of lead generation all the three libraries were evaluated for their antithrombin activity in vivo. en
dc.format.extent 122786 bytes
dc.format.extent 53757 bytes
dc.format.mimetype application/pdf
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CDRI Communication no. 6071 en
dc.title Combinatorial synthesis and biological evaluation of isoxazole-based libraries as antithrombotic agents en
dc.title.alternative Corrigendum to ‘‘Combinatorial Synthesis and Biological Evaluation of Isoxazole-Based Libraries as Antithrombotic Agents’’ [Bioorg. Med. Chem. Lett. 12 (2002) 1905] en
dc.type Article en


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