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dc.contributor.authorLeino, Teppo O.
dc.contributor.authorSieger, Peter
dc.contributor.authorYli-Kauhaluoma, Jari
dc.contributor.authorWallén, Erik A.A.
dc.contributor.authorKley, Jörg T.
dc.date.accessioned2022-04-26T06:06:39Z
dc.date.available2022-04-26T06:06:39Z
dc.date.issued2022
dc.identifier.citationLeino, T. O., Sieger, P., Yli-Kauhaluoma, J., Wallén, E. A., & Kley, J. T. (2022). The azulene scaffold from a medicinal chemist's perspective : Physicochemical and in vitro parameters relevant for drug discovery. <i>European Journal of Medicinal Chemistry</i>, <i>237</i>, Article 114374. <a href="https://doi.org/10.1016/j.ejmech.2022.114374" target="_blank">https://doi.org/10.1016/j.ejmech.2022.114374</a>
dc.identifier.otherCONVID_118852176
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/80698
dc.description.abstractAzulene is a bicyclic scaffold rarely applied in medicinal chemistry. Here we report physicochemical and in vitro parameters relevant for drug discovery for a series of diversely substituted azulenes. We synthesized and characterized several scaffold hopping series of analogously substituted azulenes, indoles and naphthalenes. This enabled a comparison of azulene with the more common scaffolds indole and naphthalene. Our data indicates that undesirably low photostability of azulenes is restricted to certain substitution patterns. Generally, we conclude that azulene is an underused lipophilic bicycle and should be considered as a valuable complement to the collection of medicinal chemistry scaffolds.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesEuropean Journal of Medicinal Chemistry
dc.rightsCC BY 4.0
dc.subject.otherIndole
dc.subject.otherNaphthalene
dc.subject.otherPhotostability
dc.subject.otherScaffold hopping
dc.titleThe azulene scaffold from a medicinal chemist's perspective : Physicochemical and in vitro parameters relevant for drug discovery
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202204262374
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiaineOrganic Chemistryen
dc.contributor.oppiaineNanoscience Centeren
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn0223-5234
dc.relation.volume237
dc.type.versionpublishedVersion
dc.rights.copyright© 2022 the Authors
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber330800
dc.subject.ysoatsuleeni
dc.subject.ysolääkesuunnittelu
dc.subject.ysoaromaattiset yhdisteet
dc.subject.ysolääkekemia
dc.subject.ysobiologinen aktiivisuus
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p38581
jyx.subject.urihttp://www.yso.fi/onto/yso/p25180
jyx.subject.urihttp://www.yso.fi/onto/yso/p23502
jyx.subject.urihttp://www.yso.fi/onto/yso/p25557
jyx.subject.urihttp://www.yso.fi/onto/yso/p24582
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1016/j.ejmech.2022.114374
dc.relation.funderResearch Council of Finlanden
dc.relation.funderSuomen Akatemiafi
jyx.fundingprogramPostdoctoral Researcher, AoFen
jyx.fundingprogramTutkijatohtori, SAfi
jyx.fundinginformationT.O.L. acknowledges the Academy of Finland (grant no. 330800) and the Doctoral Programme in Drug Research of the University of Helsinki for financial support.
dc.type.okmA1


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