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Authordc.contributor.authorSeldes, A. M. 
Authordc.contributor.authorGros, E. G. 
Authordc.contributor.authorSuarez, A. 
Authordc.contributor.authorRovirosa, Juana 
Authordc.contributor.authorSan Martín Barrientos, Aurelio 
Admission datedc.date.accessioned2018-12-20T14:06:41Z
Available datedc.date.available2018-12-20T14:06:41Z
Publication datedc.date.issued1988
Cita de ítemdc.identifier.citationTetrahedron, Volumen 44, Issue 5, 2018, Pages 1359-1362
Identifierdc.identifier.issn00404020
Identifierdc.identifier.other10.1016/S0040-4020(01)85914-7
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/153948
Abstractdc.description.abstractThe sponge Esperiopsis edwardii was examined for its steroids. It contains forty-three C27-C29 derivatives with four different types of nucleus: 3 β-hydroxy-Δ5-; 3β-hydroxy-5αH-; 3α-hydroxy-5α H- and 3-keto-Δ4-derivatives. The four groups present similar side-chain patterns and identical GC profiles. Those sterols having the 3α-hydroxy-5αH-structural configuration constitute a new group of natural products. © 1988.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceTetrahedron
Keywordsdc.subjectBiochemistry
Keywordsdc.subjectDrug Discovery
Keywordsdc.subjectOrganic Chemistry
Títulodc.titleNovel sterols from the sponge esperiopsis edwardii
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile