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Author | dc.contributor.author | Seldes, A. M. | |
Author | dc.contributor.author | Gros, E. G. | |
Author | dc.contributor.author | Suarez, A. | |
Author | dc.contributor.author | Rovirosa, Juana | |
Author | dc.contributor.author | San Martín Barrientos, Aurelio | |
Admission date | dc.date.accessioned | 2018-12-20T14:06:41Z | |
Available date | dc.date.available | 2018-12-20T14:06:41Z | |
Publication date | dc.date.issued | 1988 | |
Cita de ítem | dc.identifier.citation | Tetrahedron, Volumen 44, Issue 5, 2018, Pages 1359-1362 | |
Identifier | dc.identifier.issn | 00404020 | |
Identifier | dc.identifier.other | 10.1016/S0040-4020(01)85914-7 | |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/153948 | |
Abstract | dc.description.abstract | The 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. | |
Lenguage | dc.language.iso | en | |
Type of license | dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
Link to License | dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
Source | dc.source | Tetrahedron | |
Keywords | dc.subject | Biochemistry | |
Keywords | dc.subject | Drug Discovery | |
Keywords | dc.subject | Organic Chemistry | |
Título | dc.title | Novel sterols from the sponge esperiopsis edwardii | |
Document type | dc.type | Artículo de revista | |
Cataloguer | uchile.catalogador | SCOPUS | |
Indexation | uchile.index | Artículo de publicación SCOPUS | |
uchile.cosecha | uchile.cosecha | SI | |
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