| Literature DB >> 25147611 |
Erin M Skoda1, Joshua R Sacher1, Mustafa Z Kazancioglu1, Jaideep Saha1, Peter Wipf1.
Abstract
Low aqueous solubility is a common challenge in drug discovery and development and can lead to inconclusive biological assay results. Attaching small, polar groups that do not interfere with the bioactivity of the pharmacophore often improves solubility, but there is a dearth of viable neutral moieties available for this purpose. We have modified several poorly soluble drugs or drug candidates with the oxetanyl sulfoxide moiety of the DMSO analog MMS-350 and noted in most cases a moderate to large improvement of aqueous solubility. Furthermore, the membrane permeability of a test sample was enhanced compared to the parent compound.Entities:
Keywords: Aqueous solubility; JP4-039; MMS-350; oxetane; sulfoxide
Year: 2014 PMID: 25147611 PMCID: PMC4137373 DOI: 10.1021/ml5001504
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345