Ciencias,UNAM

Cytotoxic isoflavans from Eysenhardtia polystachya

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dc.contributor.author Alvarez, L
dc.contributor.author Ríos, MY
dc.contributor.author Esquivel, C
dc.contributor.author Chavez, MI
dc.contributor.author Delgado, G
dc.contributor.author Aguilar, MI
dc.contributor.author Villarreal, ML
dc.contributor.author Navarro, V
dc.date.accessioned 2011-01-22T10:27:49Z
dc.date.available 2011-01-22T10:27:49Z
dc.date.issued 1998
dc.identifier.issn 0163-3864
dc.identifier.uri http://hdl.handle.net/11154/2770
dc.description.abstract Two new cytotoxic isoflavans, (3S)-7-hydroxy-2',3',4',5',8-pentamethox (1) and (3S)3',7-dihydroxy-2',4', 5', 8-tetramethoxyisoflavan (2), were isolated from the bark and trunks of Eysenhardtia polystachya (Leguminosae), together with the known constituents stigmasterol, isoduartin, cuneatin, 7-hydroxy-2',4',5'-trimethoxyisoflavone, and 3,4-dimethoxy-8,9-(methylenedioxy)pterocarpan. The structures of 1 and 2 were elucidated on the basis of spectroscopic methods. The antimicrobial, cytotoxic, and insecticidal potential of some of these compounds were evaluated. The isoflavans 1, 2, and isoduartin (2',7-dihydroxy-3',4',8-trimethoxyisoflavan) displayed moderate cytotoxic activity against KB cell lines. en_US
dc.language.iso en en_US
dc.title Cytotoxic isoflavans from Eysenhardtia polystachya en_US
dc.type Article en_US
dc.identifier.idprometeo 2838
dc.source.novolpages 61(6):767-770
dc.subject.wos Plant Sciences
dc.subject.wos Chemistry, Medicinal
dc.subject.wos Pharmacology & Pharmacy
dc.description.index WoS: SCI, SSCI o AHCI
dc.relation.journal Journal of Natural Products

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