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Article: Cimigenol-3-O-β-D-xylopranoside methanol solvate

TitleCimigenol-3-O-β-D-xylopranoside methanol solvate
Authors
Issue Date2006
Citation
Acta Crystallographica Section E: Structure Reports Online, 2006, v. 62, n. 11 How to Cite?
AbstractThe title compound, (23R,24S)-16b,23:16a,24-diepoxy-15a,25-dihydroxy-9,19- cyclolanostane-3-O-β-D-xylopyranoside methanol solvate, C 35H56O9·CH4O, is a cycloartane triterpene glycoside which was isolated from the rhizomes of Actaea asiatica. The molecule contains five six-membered rings, two five-membered rings and a three-membered ring. The crystal structure is stabilized by intra- and intermolecular O - H⋯O hydrogen bonds. © 2006 International Union of Crystallography All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/342694
ISSN
2011 Impact Factor: 0.347
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorFan, Yunshuang-
dc.contributor.authorJia, Wei-
dc.contributor.authorTakaishi, Yoshihisa-
dc.contributor.authorDuan, Hong Quan-
dc.date.accessioned2024-04-17T07:05:35Z-
dc.date.available2024-04-17T07:05:35Z-
dc.date.issued2006-
dc.identifier.citationActa Crystallographica Section E: Structure Reports Online, 2006, v. 62, n. 11-
dc.identifier.issn1600-5368-
dc.identifier.urihttp://hdl.handle.net/10722/342694-
dc.description.abstractThe title compound, (23R,24S)-16b,23:16a,24-diepoxy-15a,25-dihydroxy-9,19- cyclolanostane-3-O-β-D-xylopyranoside methanol solvate, C 35H56O9·CH4O, is a cycloartane triterpene glycoside which was isolated from the rhizomes of Actaea asiatica. The molecule contains five six-membered rings, two five-membered rings and a three-membered ring. The crystal structure is stabilized by intra- and intermolecular O - H⋯O hydrogen bonds. © 2006 International Union of Crystallography All rights reserved.-
dc.languageeng-
dc.relation.ispartofActa Crystallographica Section E: Structure Reports Online-
dc.titleCimigenol-3-O-β-D-xylopranoside methanol solvate-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1107/S1600536806040153-
dc.identifier.scopuseid_2-s2.0-33750884381-
dc.identifier.volume62-
dc.identifier.issue11-
dc.identifier.eissn1600-5368-
dc.identifier.isiWOS:000241691500205-

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