Oxadiazole isomers: all bioisosteres are not created equal
2012 (English)In: MedChemComm, ISSN 2040-2503, Vol. 3, no 5, 600-604 p.Article in journal (Refereed) Published
Two series of amino-substituted 1,2,4- and 1,3,4-oxadiazole matched compounds were evaluated and found to have significant differences in their various physical and pharmaceutical properties. Experimental and computational techniques suggested that variation in hydrogen bond acceptor and donor strength were responsible for these effects.
Place, publisher, year, edition, pages
2012. Vol. 3, no 5, 600-604 p.
article, drug half life, drug protein binding, drug solubility, drug stability, drug structure, drug synthesis, human, hydrogen bond, isomer, lipophilicity, mouse, nonhuman, plasma protein binding, priority journal, rat, structure analysis, substitution reaction
Biochemistry and Molecular Biology
IdentifiersURN: urn:nbn:se:kth:diva-98021DOI: 10.1039/c2md20054fISI: 000304387300010ScopusID: 2-s2.0-84860429692OAI: oai:DiVA.org:kth-98021DiVA: diva2:535006
QC 201206192012-06-192012-06-182012-06-19Bibliographically approved