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Will 1,2-dihydro-1,2-azaborine-based drugs resist metabolism by cytochrome P450 compound I?

dc.contributor.authorSilva, Pedro J.
dc.date.accessioned2019-09-12T08:39:27Z
dc.date.available2019-09-12T08:39:27Z
dc.date.issued2016-07
dc.description.abstract1,2-dihydro-1,2-azaborine is a structural and electronic analogue of benzene which is able to occupy benzene-binding pockets in T4 lysozyme and has been proposed as suitable arene-mimicking group for biological and pharmaceutical applications. Its applicability in a biological context requires it to be able to resist modification by xenobiotic-degrading enzymes like the P450 cytochromes. Quantum chemical computations described in this work show that 1,2-dihydro-1,2-azaborine is much more prone to modification by these enzymes than benzene, unless steric crowding of the ring prevents it from reaching the active site, or otherwise only allows reaction at the less reactive C4-position. This novel heterocyclic compound is therefore expected to be of limited usefulness as an aryl bioisostere.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSilva, P.J. (2016). Will 1,2-dihydro-1,2-azaborine-based drugs resist metabolism by cytochrome P450 compound I? PeerJ. https://doi.org/10.7717/peerj.2299. ISSN 2167-8359.
dc.identifier.doi10.7717/peerj.2299pt_PT
dc.identifier.issn2167-8359
dc.identifier.urihttp://hdl.handle.net/10284/7823
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.relation.publisherversiondx.doi.org/10.7717/peerj.2299pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectQuantum computationspt_PT
dc.subjectDensity-functional theorypt_PT
dc.subjectReactivity
dc.subjectAzaborine
dc.subjectXenobiotics
dc.titleWill 1,2-dihydro-1,2-azaborine-based drugs resist metabolism by cytochrome P450 compound I?pt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.titlePeerJpt_PT
person.familyNameSilva
person.givenNamePedro
person.identifier.orcid0000-0001-9316-9275
person.identifier.scopus-author-id55310885700
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationf4a9230e-0a0e-45b6-b894-e71ded186ef2
relation.isAuthorOfPublication.latestForDiscoveryf4a9230e-0a0e-45b6-b894-e71ded186ef2

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