Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5053
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAnuradha V
dc.contributor.authorSrinivas P.V
dc.contributor.authorRanga Rao R
dc.contributor.authorManjulatha K
dc.contributor.authorPurohit M.G
dc.contributor.authorMadhusudana Rao J.
dc.date.accessioned2020-06-12T15:06:03Z-
dc.date.available2020-06-12T15:06:03Z-
dc.date.issued2006
dc.identifier.citationBioorganic and Medicinal Chemistry , Vol. 14 , 20 , p. 6820 - 6826en_US
dc.identifier.uri10.1016/j.bmc.2006.06.048
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5053-
dc.description.abstractTwo new furanoflavonoids (1, 2), one new chalcone dimer (3) along with six known compounds, chrysophanol, 5-O-methyl squarrosin, 5-methoxy furano[4?,5?,6,7]flavone, calodenone, lophirone A and lophirone H were isolated from the ethyl acetate-soluble fraction of methanol extract of root bark of Ochna squarrosa. Chrysophanol, calodenone, lophirone A and lophirone H were isolated from this plant for the first time. The structures of all the isolated compounds were confirmed by 1D and 2D spectroscopic data. These compounds were tested for analgesic and anti-inflammatory activity. All the new compounds showed good analgesic and anti-inflammatory activity. A simple and facile method for the cleavage of benzyl ethers using I2 in trigol is also reported. © 2006 Elsevier Ltd. All rights reserved.en_US
dc.subjectAnalgesic activity
dc.subjectAnti-inflammatory activity
dc.subjectChalcone dimer
dc.subjectFuranoflavanoid
dc.subjectOchna squarrosa
dc.titleIsolation and synthesis of analgesic and anti-inflammatory compounds from Ochna squarrosa L.en_US
dc.typeArticle
Appears in Collections:1. Journal Articles

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.