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Updated: Oct 10, 2026

Structure-Guided Design and Development of Novel Cyclophilin A Inhibitors and Ganoderiol-F Derivatives: An In-Silico Approach
Published on: June 23, 2026
Isosterism among analogues of torasemide: conformational, electronic and lipophilic properties
J Wouters1, C Michaux, F Durant
1Laboratory of Molecular Structure and Department of Pharmacy, Facultés Universitaires Notre Dame de la Paix, Namur, Belgium.
Abstract:
The structures, electronic (charges, molecular electrostatic potential, molecular orbitals) and lipophilic properties of three isostere analogues of torasemide were determined and the influence of the replacement of the sulfonyl urea group on the conformation and electronic properties of the molecules is discussed. Lipophilicity of the compounds seems to be the most discriminating property along the series and affects their pharmacological activities.
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