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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/13477
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dc.contributor.authorGaikwad, Anil Bhanudas-
dc.date.accessioned2023-12-21T04:40:02Z-
dc.date.available2023-12-21T04:40:02Z-
dc.date.issued2016-
dc.identifier.urihttps://www.ingentaconnect.com/content/ben/cdr/2016/00000012/00000003/art00007-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13477-
dc.description.abstractFoxO1, one of the most widely expressed sub-families of the winged helix forkhead factors, is biologically ‘omni-functional’ owing to its far-flung roles in metabolism, cell cycle, tissue differentiation and development and oxidative stress response. The knowledge of involvement of FoxO1 in metabolic disorders has long been there, but the potential target remained underutilized due to unavailability of specific and potent inhibitors. The review provides an insight into the role of FoxO1 in orchestrating metabolic diseases’ pathogenesis (including diabetes, its secondary complications and obesity) and compiles the literature on FoxO1 inhibitors. The emergence of various natural molecules and synthesized small molecules like AS1842856 as FoxO1 inhibitors urges us to think further and decide the future course of drug development for the management of metabolic disorders.en_US
dc.language.isoenen_US
dc.publisherBentham Scienceen_US
dc.subjectPharmacyen_US
dc.subjectAS1842856en_US
dc.subjectFoxO1en_US
dc.subjectMetabolic disordersen_US
dc.subjectObesityen_US
dc.subjectDiabetic complicationsen_US
dc.titleFoxO1 Inhibitors: The Future Medicine for Metabolic Disorders?en_US
dc.typeArticleen_US
Appears in Collections:Department of Pharmacy

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