Acta Crystallographica Section E: Crystallographic Communications (May 2017)

Crystal structure and Hirshfeld surface analysis of 3-oxours-12-ene-27a,28-dioic acid (quafrinoic acid)

  • Jean Jules Bankeu Kezetas,
  • Stéphanie Dietagoum Madjouka,
  • Rajesh Kumar,
  • Muhammad Shaiq Ali,
  • Bruno Lenta Njakou,
  • Sammer Yousuf

DOI
https://doi.org/10.1107/S2056989017006077
Journal volume & issue
Vol. 73, no. 5
pp. 763 – 766

Abstract

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The title compound, C30H44O5, is a pentacyclic triterpene isolated from the Cameroonian medicinal plant Nauclea Pobeguinii and known as quafrinoic acid. The molecule is composed of five fused six-membered rings, four of which adopt a chair conformation and one a half-chair conformation. Intramolecular C—H...O hydrogen-bond interactions exist, which generate S6 and S8 rings. In the crystal, molecules are linked by pairs of O—H...O hydrogen bonds, linking R22(8) rings into chains running parallel to the a axis; these chains are further connected into layers parallel to the ab plane by C—H...O hydrogen bonds. The Hirshfeld surface analysis of the crystal structure indicates that the most important contributions for the crystal packing are from H...H (79.4%) and O...H (20.4%) interactions.

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