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dc.contributor.authorDeka, N.
dc.contributor.authorBajare, S.
dc.contributor.authorAnthony, J.
dc.contributor.authorNair, A.
dc.contributor.authorDamre, A.
dc.contributor.authorPatel, Dharmeshkumar
dc.contributor.authorB-Rao, C.
dc.contributor.authorSivaramakrishnan, H.
dc.contributor.authorMutt, S.
dc.contributor.authorWilankar, C.
dc.contributor.authorMarita, R.
dc.date.accessioned2017-11-28T06:36:43Z
dc.date.available2017-11-28T06:36:43Z
dc.date.created2017-11-28T06:21:50Z
dc.date.issued2013
dc.identifier.citationDeka, N. and Bajare, S. and Anthony, J. and Nair, A. and Damre, A. and Patel, D. and B-Rao, C. et al. 2013. Synthesis of N-(6-(4-(Piperazin-1-yl)phenoxy)pyridin-3-yl) benzenesulfonamide Derivatives for the Treatment of Metabolic Syndrome. International Journal of Medicinal Chemistry. 2013: Article ID 201580.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/58721
dc.identifier.doi10.1155/2013/201580
dc.description.abstract

Metabolic syndrome is a widely prevalent multifactorial disorder associated with an increased risk of cardiovascular disease and type 2 diabetes mellitus. High plasma levels of insulin and glucose due to insulin resistance are a major component of the metabolic disorder. Thiazolidinediones (TZDs) are potent PPARγ ligand and used as insulin sensitizers in the treatment of type 2 diabetes mellitus. They are potent insulin-sensitizing agents but due to adverse effects like hepatotoxicity, a safer alternative of TZDs is highly demanded. Here we report synthesis of N-(6-(4-(piperazin-1-yl)phenoxy)pyridin-3-yl)benzenesulfonamide derivatives as an alternate remedy for insulin resistance.

dc.publisherHindawi Ltd
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/
dc.titleSynthesis of N-(6-(4-(Piperazin-1-yl)phenoxy)pyridin-3-yl) benzenesulfonamide Derivatives for the Treatment of Metabolic Syndrome
dc.typeJournal Article
dcterms.source.issn2090-2069
dcterms.source.titleInternational Journal of Medicinal Chemistry
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusOpen access


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