Investigation of structure-activity relationship on 17-spirolactone derivatives: the electronic-topological approach

dc.contributor.authorKandemirli, F
dc.contributor.authorTokay, N
dc.contributor.authorShvets, NM
dc.contributor.authorDimoglo, AS
dc.date.accessioned2025-10-29T11:21:06Z
dc.date.issued2002
dc.departmentFakülteler, Temel Bilimler Fakültesi, Kimya Bölümü
dc.description3rd International Symposium on Pharmaceutical Chemistry (ISPC-3) -- SEP 15-17, 2001 -- ISTANBUL, TURKEY
dc.description.abstractSixty steroid homologues belonging to a series of 17-spirolactone derivatives such as aldosterone antagonists were investigated by electronic-topological method (ETM). Activity features Ph1-Ph3 that also are called pharmacophores were revealed. The pharmacophore Ph1 consists of two oxygen atoms and four carbon atoms. The mineralocorticoid activity appeared to be affected by the distance between the two oxygen atoms. Features AP1-AP3 that are characteristic of inactive compounds (or anti-pharmacophores) were also revealed. Comparative analysis of molecules that include either pharmacophores or anti-pharmacophores was carried out. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
dc.description.sponsorshipDept Pharmaceut Chem,Fac Pharmacy,Hacettepe Univ
dc.identifier.doi10.1016/S0014-827X(02)01256-9
dc.identifier.endpage607
dc.identifier.issn0014-827X
dc.identifier.issue7
dc.identifier.pmid12164222
dc.identifier.startpage601
dc.identifier.urihttps://doi.org/10.1016/S0014-827X(02)01256-9
dc.identifier.urihttps://hdl.handle.net/20.500.14854/8875
dc.identifier.volume57
dc.identifier.wosWOS:000177620000018
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherElsevier Science Sa
dc.relation.ispartofFarmaco
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20251020
dc.subjectelectronic-topological method
dc.subjectmineralocorticoids
dc.subjectaldosterone
dc.titleInvestigation of structure-activity relationship on 17-spirolactone derivatives: the electronic-topological approach
dc.typeConference Object

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