The crystal structure of a Li+ salt of a glucosyl derivative of lithocholic acid (lithium 3a-(a-D-glucopyranosyl)- 5b-cholan-24-oate) has been solved. The crystal belongs to the orthorhombic system, P212121 spatial group, and includes acetone and water in the structure with a 1:1:2 stoichiometry. Monolayers, having a hydrophobic interior and hydrophilic edges, are recognized in the crystal structure. Li+ is coordinated to three hydroxyl groups of three different glucose residues, with two of them belonging to the same monolayer. A fourth molecule, located in this monolayer, is involved in the coordination of the cation through the carboxylate ion by an electrostatic interaction, thus completing a distorted tetrahedron. All Li+-oxygen distances values are very close to the sum of the ionic radius of Li+ and van der Waals radius of oxygen. Each steroid molecule is linked to other five steroid molecules through hydrogen bonds. Water and acetone are also involved in the hydrogen bond network. A hierarchical organization can be recognized in the crystal, the helical assembly along 21 screw axes being left handed.

Crystal structure of a lithium salt of a glucosyl derivative of lithocholic acid / Gubitosi, Marta; Meijide, Francisco; D'Annibale, Andrea; Vázquez Tato, José; Jover, Aida; Galantini, Luciano; Travaglini, Leana; DI GREGORIO, MARIA CHIARA; Pavel, Nicolae Viorel. - In: STEROIDS. - ISSN 0039-128X. - STAMPA. - 113:(2016), pp. 87-94. [10.1016/j.steroids.2016.07.001]

Crystal structure of a lithium salt of a glucosyl derivative of lithocholic acid

GUBITOSI, MARTA;D'ANNIBALE, Andrea;GALANTINI, Luciano;TRAVAGLINI, Leana;DI GREGORIO, MARIA CHIARA;PAVEL, Nicolae Viorel
2016

Abstract

The crystal structure of a Li+ salt of a glucosyl derivative of lithocholic acid (lithium 3a-(a-D-glucopyranosyl)- 5b-cholan-24-oate) has been solved. The crystal belongs to the orthorhombic system, P212121 spatial group, and includes acetone and water in the structure with a 1:1:2 stoichiometry. Monolayers, having a hydrophobic interior and hydrophilic edges, are recognized in the crystal structure. Li+ is coordinated to three hydroxyl groups of three different glucose residues, with two of them belonging to the same monolayer. A fourth molecule, located in this monolayer, is involved in the coordination of the cation through the carboxylate ion by an electrostatic interaction, thus completing a distorted tetrahedron. All Li+-oxygen distances values are very close to the sum of the ionic radius of Li+ and van der Waals radius of oxygen. Each steroid molecule is linked to other five steroid molecules through hydrogen bonds. Water and acetone are also involved in the hydrogen bond network. A hierarchical organization can be recognized in the crystal, the helical assembly along 21 screw axes being left handed.
2016
bile salt; crystal structure; glucosyl derivative; hierarchical organization; lithium salt; lithocholic acid; biochemistry; molecular biology; pharmacology; endocrinology; clinical biochemistry; organic chemistry
01 Pubblicazione su rivista::01a Articolo in rivista
Crystal structure of a lithium salt of a glucosyl derivative of lithocholic acid / Gubitosi, Marta; Meijide, Francisco; D'Annibale, Andrea; Vázquez Tato, José; Jover, Aida; Galantini, Luciano; Travaglini, Leana; DI GREGORIO, MARIA CHIARA; Pavel, Nicolae Viorel. - In: STEROIDS. - ISSN 0039-128X. - STAMPA. - 113:(2016), pp. 87-94. [10.1016/j.steroids.2016.07.001]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/900445
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