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dc.contributor.authorValkonen, Arto
dc.contributor.authorKoivukorpi, Juha
dc.contributor.authorLahtinen, Manu
dc.contributor.authorKolehmainen, Erkki
dc.date.accessioned2016-12-19T07:58:19Z
dc.date.available2016-12-19T07:58:19Z
dc.date.issued2009
dc.identifier.citationValkonen, A., Koivukorpi, J., Lahtinen, M., & Kolehmainen, E. (2009). 3a-hydroxy-N-(3-hydroxypropyl)-5b-cholan-24-amide. <i>Acta Crystallographica Section E</i>, <i>E65</i>, o650.
dc.identifier.otherCONVID_18648216
dc.identifier.otherTUTKAID_35007
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/52417
dc.description.abstractThe title compound, C27H47NO3, is a (3-hydroxypropyl)amide derivative of naturally occurring enantiopure lithocholic acid (3-hydroxy-5-cholan-24-oic acid). The molecule contains four fused rings: three six-membered rings in chair conformations and one five-membered ring in a half-chair form. The two terminal six-membered rings are cis-fused, while other rings are trans-fused. The structure contains an intramolecular O—H O hydrogen bond and a similar hydrogen-bond framework to the corresponding deoxycholic and chenodeoxycholic acid derivatives. Intermolecular O— H O and N—H O interactions are also present in the crystal. This compound seems to have at least two polymorphic forms from a comparison of the X-ray powder pattern simulated from the present structure of the title compound and that previously obtained for the powder sample.
dc.language.isoeng
dc.publisherIuCr
dc.relation.ispartofseriesActa Crystallographica Section E
dc.subject.otherrakennekemia
dc.subject.othersappihappojohdannainen
dc.subject.otherstructural chemistry
dc.subject.otherbile acid derivative
dc.title3a-hydroxy-N-(3-hydroxypropyl)-5b-cholan-24-amide
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201612135069
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2016-12-13T10:15:21Z
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.format.pagerangeo650
dc.relation.volumeE65
dc.type.versionpublishedVersion
dc.rights.copyright© the Authors, 2009. This is an open access article distributed under the Creative Commons Attribution (CC-BY) Licence.
dc.rights.accesslevelopenAccessfi
dc.rights.urlhttps://creativecommons.org/licenses/by/2.0/uk/legalcode
dc.relation.doi10.1107/S1600536809006862


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© the Authors, 2009. This is an open access article distributed under the Creative Commons Attribution (CC-BY) Licence.
Except where otherwise noted, this item's license is described as © the Authors, 2009. This is an open access article distributed under the Creative Commons Attribution (CC-BY) Licence.