Revisiting the absolute chirality and polymorphism of (-)-Istanbulin A

Acta Crystallogr C Struct Chem. 2020 Sep 1;76(Pt 9):914-920. doi: 10.1107/S2053229620011493. Epub 2020 Aug 28.

Abstract

The terpenoid (-)-Istanbulin A is a natural product isolated from Senecio filaginoides DC, one of the 270 species of Senecio (Asteraceae) which occurs in Argentina. The structure and absolute configuration of this compound [9a-hydroxy-3,4a,5-trimethyl-4a,6,7,8a,9,9a-hexahydro-4H,5H-naphtho[2,3-b]-furan-2,8-dione or (4S,5R,8R,10S)-1-oxo-8β-hydroxy-10βH-eremophil-7(11)-en-12,8β-olide, C15H20O4] were determined by single-crystal X-ray diffraction studies. It proved to be a sesquiterpene lactone showing an eremophilanolide skeleton whose chirality is described as 4S,5R,8R,10S. Structural results were also in agreement with the one- and two-dimensional (1D and 2D) NMR and HR-ESI-MS data, and other complementary spectroscopic information. In addition, (-)-Istanbulin A is a polymorph of the previously reported form of (-)-Istanbulin A, form I; thus, the title compound is denoted form II or polymorph II. Structural data and a literature search allowed the chirality of Istanbulin A to be revisited. The antimicrobial and antifungal activities of (-)-Istanbulin A, form II, were evaluated in order to establish a reference for future comparisons and applications related to specific crystal forms of Istanbulins.

Keywords: Istanbulin; Senecio filaginoides; absolute configuration; antimicrobial activity; crystal structure; natural product; polymorphism; terpenoid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents / chemistry*
  • Crystallography, X-Ray
  • Furans / chemistry*
  • Hydrogen Bonding
  • Magnetic Resonance Spectroscopy
  • Sesquiterpenes / chemistry*
  • Stereoisomerism

Substances

  • Antifungal Agents
  • Furans
  • Sesquiterpenes
  • istanbulin A