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Development of submicromolar 17 beta-HSD10 inhibitors and their in vitro and in vivo evaluation

dc.contributor.authorBenek, Ondřej
dc.contributor.authorVašková, Michaela
dc.contributor.authorSedláček Miškeříková, Markéta
dc.contributor.authorSchmidt, Monika
dc.contributor.authorAndrýs, Rudolf
dc.contributor.authorRotterová, Aneta
dc.contributor.authorSkarka, Adam
dc.contributor.authorHatlapatkova, Jana
dc.contributor.authorKarasova, Jana Zdarova
dc.contributor.authorMedvecký, Matej
dc.contributor.authorHroch, Lukas
dc.contributor.authorVinklářová, Lucie
dc.contributor.authorFisar, Zdenek
dc.contributor.authorHroudova, Jana
dc.contributor.authorHandl, Jiri
dc.contributor.authorCapek, Jan
dc.contributor.authorRousar, Tomas
dc.contributor.authorKobrlova, Tereza
dc.contributor.authorDolezal, Rafael
dc.contributor.authorSoukup, Ondrej
dc.contributor.authorAitken, Laura
dc.contributor.authorGunn-Moore, Frank
dc.contributor.authorMusílek, Kamil
dc.date.accessioned2025-12-05T13:00:18Z
dc.date.available2025-12-05T13:00:18Z
dc.date.issued2023
dc.description.abstract17 beta-hydroxysteroid dehydrogenase type 10 (17 beta-HSD10) is a multifunctional mitochondrial enzyme and putative drug target for the treatment of various pathologies including Alzheimer's disease or some types of hormone-dependent cancer. In this study, a series of new benzothiazolylurea-based inhibitors were developed based on the structure-activity relationship (SAR) study of previously published compounds and predictions of their physicochemical properties. This led to the identification of several submicromolar inhibitors (IC50 similar to 0.3 mu M), the most potent compounds within the benzothiazolylurea class known to date. The positive interaction with 17 beta-HSD10 was further confirmed by differential scanning fluorimetry and the best molecules were found to be cell penetrable. In addition, the best compounds weren't found to have additional effects for mitochondrial off-targets and cytotoxic or neurotoxic effects. The two most potent inhibitors 9 and 11 were selected for in vivo pharmacokinetic study after intravenous and peroral administration. Although the pharmacokinetic results were not fully conclusive, it seemed that compound 9 was bioavailable after peroral administration and could penetrate into the brain (brain-plasma ratio 0.56).eng
dc.formatp. &quot;Article Number: 115593&quot;
dc.identifier.doi10.1016/j.ejmech.2023.115593
dc.identifier.issn0223-5234
dc.identifier.obd43880215
dc.identifier.urihttp://hdl.handle.net/20.500.12603/1857
dc.identifier.wos001030059600001
dc.language.isoeng
dc.peerreviewedyes
dc.publicationstatuspostprint
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
dc.relation.ispartofEuropean Journal of Medicinal Chemistry, volume 258, issue: říjeneng
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0223523423005597?via%3Dihub
dc.rights.accessOpen Access
dc.rights.licenseCC BY
dc.source.urlhttps://www.sciencedirect.com/science/article/pii/S0223523423005597?via%3Dihub
dc.subjectAmyloid-binding alcohol dehydrogenase (ABAD)eng
dc.subjectAlzheimers diseaseeng
dc.subject17 beta-hydroxysteroid dehydrogenase type 10 (17 beta-HSD10)eng
dc.subjectEnzyme inhibitioneng
dc.subjectPharmacokineticseng
dc.titleDevelopment of submicromolar 17 beta-HSD10 inhibitors and their in vitro and in vivo evaluationeng
dc.typearticle

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