Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/3423
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dc.contributor.authorSrivastava, Shefali-
dc.contributor.authorRaj, Kanwal-
dc.contributor.authorKhare, Pratibha-
dc.contributor.authorBhaduri, Amiya P-
dc.contributor.authorChander, Ramesh-
dc.contributor.authorRaghubir, Ram-
dc.contributor.authorMahendra, K-
dc.contributor.authorRao, C V Narsimha-
dc.contributor.authorPrabhu, S R-
dc.date.accessioned2009-03-20T08:33:02Z-
dc.date.available2009-03-20T08:33:02Z-
dc.date.issued2009-02-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/3423-
dc.description237-247en_US
dc.description.abstractA series of compounds 2a-g, 3a,b, 4a-n have been synthesized from solanesol 1, an acyclic terpenoid alcohol, extracted from tobacco waste. These compounds have been evaluated for antioxidant, angiogenesis and wound healing activity. Compounds 3b and 4h exhibit better wound healing activity in comparison to 3,3-dimethylacryl shikonin. These results indicate that Solanesol derivatives can be further developed as wound healing agents.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.48B(2) [February 2009]en_US
dc.subjectSolanesolen_US
dc.subjectAngiogenesisen_US
dc.subjectAntioxidanten_US
dc.subjectWound healing activityen_US
dc.titleNovel hybrid natural products derived from solanesol as wound healing agentsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.48B(02) [February 2009]

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