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A new sesquiterpene-coumarin ether and a new abietane diterpene and their effects as inhibitors of p-glycoprotein

dc.contributor.authorMadureira, AM
dc.contributor.authorMolnar, A
dc.contributor.authorAbreu, PM
dc.contributor.authorMolnar, J
dc.contributor.authorFerreira, MJU
dc.date.accessioned2015-12-30T10:17:06Z
dc.date.available2015-12-30T10:17:06Z
dc.date.issued2004
dc.description.abstractA new sesquiterpene-coumarin ether (5'beta,9'alpha,10'alpha)-7-O-(3alpha-methoxy-8'(12')-drimen-11'-yl) -scopoletin, designated driportlandin (1) and a new abietane quinoid diterpene 16-hydroxyabieta-8,12-diene-11,14-dione, named portlanquinol (2) together with lupeol, nepehinol, wrightial, formonetin and davidigenin were isolated and characterized from the Me2CO extract of whole dried plant of Euphorbia portlandica. The structures of the new compounds were elucidated from spectral data including 2D-NMR experiments of COSY, HMQC, HMBC and NOESY. When examined for their effects on the reversal of multidrug resistance (MDR) on mouse lymphoma cells, compound 1 proved to be more active than the positive control verapamil and compound 2 was found to be toxic. This is the first report on the isolation of a sesquiterpene-coumarin and a quinoid-type diterpenoid from Euphorbia.
dc.formatapplication/pdf
dc.identifier.citationPLANTA MEDICA. - Vol. 70, n. 9 (SEP 2004), p. 828-833
dc.identifier.doihttp://dx.doi.org/10.1055/s-2004-827231
dc.identifier.issn0032-0943
dc.identifier.urihttp://hdl.handle.net/10451/20928
dc.language.isoeng
dc.publisherGEORG THIEME VERLAG KG
dc.subjectPlant Sciences
dc.subjectChemistry, Medicinal
dc.subjectPharmacology & Pharmacy
dc.titleA new sesquiterpene-coumarin ether and a new abietane diterpene and their effects as inhibitors of p-glycoprotein
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage833por
oaire.citation.startPage828por
oaire.citation.titlePLANTA MEDICApor
oaire.citation.volumeVol. 70por
rcaap.rightsrestrictedAccess
rcaap.typearticle

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