Published in

Bentham Science Publishers, Letters in Drug Design & Discovery, 8(7), p. 610-617

DOI: 10.2174/157018010792062731

Links

Tools

Export citation

Search in Google Scholar

Lithocholic Acid Derivative as a Model for Artificial Receptors: A Raman Study

This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

Two lithocholic acid (LCA) derivatives — mono- and diesters (newly synthetised) — are studied for their main conformational preferences, by Raman spectroscopy coupled to theoretical (DFT) methods. Raman bands characteristic of each compound were assigned, allowing an accurate and rapid identification of this kind of systems. The conformational preferences of the LCA diester were related with its ability to function as a model for artificial receptors, displaying a tailored structural profile.