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3?-Hydr-oxy-N-(3-hydroxy-prop-yl)-5?-cholan-24-amide.


ABSTRACT: The title compound, C(27)H(47)NO(3), is a (3-hydroxy-prop-yl)amide derivative of naturally occurring enanti-opure lithocholic acid (3?-hydr-oxy-5?-cholan-24-oic acid). The mol-ecule 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 intra-molecular O-H?O hydrogen bond and a similar hydrogen-bond framework to the corresponding deoxy-cholic and chenodeoxy-cholic acid derivatives. Inter-molecular O-H?O and N-H?O inter-actions 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.

SUBMITTER: Valkonen A 

PROVIDER: S-EPMC2968534 | biostudies-literature | 2009 Feb

REPOSITORIES: biostudies-literature

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3α-Hydr-oxy-N-(3-hydroxy-prop-yl)-5β-cholan-24-amide.

Valkonen Arto A   Koivukorpi Juha J   Lahtinen Manu M   Kolehmainen Erkki E  

Acta crystallographica. Section E, Structure reports online 20090228 Pt 3


The title compound, C(27)H(47)NO(3), is a (3-hydroxy-prop-yl)amide derivative of naturally occurring enanti-opure lithocholic acid (3α-hydr-oxy-5β-cholan-24-oic acid). The mol-ecule 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 intra-molecular O-H⋯O hydrogen bond and a similar hydrogen-bond framework to the c  ...[more]

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