Tunable recognition of the steroid α-face by adjacent π-electron density

Friscic, T., Lancaster, R. W., Fabian, Laszlo and Karamertzanis, P. G. (2010) Tunable recognition of the steroid α-face by adjacent π-electron density. Proceedings of the National Academy of Sciences of the United States of America (PNAS), 107 (30). pp. 13216-13221. ISSN 1091-6490

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We report a previously unknown recognition motif between the a-face of the steroid hydrocarbon backbone and p-electron-rich aromatic substrates. Our study is based on a systematic and comparative analysis of the solid-state complexation of four steroids with 24 aromatic molecules. By using the solid state as a medium for complexation, we circumvent solubility and solvent competition problems that are inherent to the liquid phase. Characterization is performed using powder and single crystal X-ray diffraction, infrared solid-state spectroscopy and is complemented by a comprehensive cocrystal structure prediction methodology that surpasses earlier computational approaches in terms of realism and complexity. Our combined experimental and theoretical approach reveals that the a?p stacking is of electrostatic origin and is highly dependent on the steroid backbone’s unsaturated and conjugated character. We demonstrate that the a?p stacking interaction can drive the assembly of molecules, in particular progesterone, into solid-state complexes without the need for additional strong interactions. It results in a marked difference in the solid-state complexation propensities of different steroids with aromatic molecules, suggesting a strong dependence of the steroid-binding af?nity and even physicochemical properties on the steroid’s A-ring structure. Hence, the hydrocarbon part of the steroid is a potentially important variable in structure-activity relationships for establishing the binding and signaling properties of steroids, and in the manufacture of pharmaceutical cocrystals.

Item Type: Article
Faculty \ School: Faculty of Science > School of Pharmacy
UEA Research Groups: Faculty of Science > Research Groups > Drug Delivery and Pharmaceutical Materials (former - to 2017)
Faculty of Science > Research Groups > Pharmaceutical Materials and Soft Matter
Depositing User: Rachel Smith
Date Deposited: 15 Mar 2011 16:14
Last Modified: 23 Oct 2022 01:26
URI: https://ueaeprints.uea.ac.uk/id/eprint/26256
DOI: 10.1073/pnas.0915142107

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