Synthesis and evaluation of new 3-phenylcoumarin derivatives as potential antidepressant agents

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dc.contributor.author Sashidhara, K V
dc.contributor.author Rao, K B
dc.contributor.author Singh, Seema
dc.contributor.author Modukuri, R K
dc.contributor.author Teja, G A
dc.contributor.author Chandasana, Hardik
dc.contributor.author Shukla, Shubha
dc.contributor.author Bhatta, R S
dc.date.accessioned 2017-04-19T06:34:26Z
dc.date.available 2017-04-19T06:34:26Z
dc.date.issued 2014
dc.identifier.citation Bioorganic & Medicinal Chemistry Letters, 2014, 24(20), 4876-4880 en
dc.identifier.uri http://hdl.handle.net/123456789/1671
dc.description.abstract A series of amine substituted 3-phenyl coumarin derivatives were designed and synthesized as potential antidepressant agents. In preliminary screening, all compounds were evaluated in forced swimming test (FST), a model to screen antidepressant activity in rodents. Among the series, compounds 5c and 6a potentially decreased the immobility time by 73.4% and 79.7% at a low dose of 0.5 mg/kg as compared to standard drug fluoxetine (FXT) which reduced the immobility time by 74% at a dose of 20 mg/kg, i.p. Additionally, these active compounds also exhibited significant efficacy in tail suspension test (TST) (another model to screen antidepressant compounds). Interestingly, rotarod and locomotor activity tests confirmed that these two compounds do not have any motor impairment effect and neurotoxicity in mice. Our studies demonstrate that the new 3-phenylcoumarin derivatives may serve as a promising antidepressant lead and hence pave the way for further investigation around this chemical space. en
dc.format.extent 297795 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CSIR-CDRI communication number is 8770 en
dc.subject Forced swim test en
dc.subject Tail suspension test en
dc.subject Depression en
dc.subject Coumarin en
dc.title Synthesis and evaluation of new 3-phenylcoumarin derivatives as potential antidepressant agents en
dc.type Article en


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