Приказ основних података о документу

dc.creatorĐaković-Sekulić, Tatjana
dc.creatorLozanov-Crvenković, Zagorka
dc.creatorRančić, Milica
dc.creatorTrišović, Nemanja
dc.creatorUšćumlić, Gordana
dc.date.accessioned2021-03-10T12:36:30Z
dc.date.available2021-03-10T12:36:30Z
dc.date.issued2014
dc.identifier.issn1082-6076
dc.identifier.urihttp://TechnoRep.tmf.bg.ac.rs/handle/123456789/2856
dc.description.abstractQuantitative structure-retention relationship (QSRR) study of retention data of thirteen 5-arylidene-2,4-thiazolidinediones obtained by reversed phase HPTLC. The effect of substituents attached to aryliden ring on the properties of TZD molecule, whose retention is closely correlated to the inhibitory activity, was investigated. PCA was used to show similarities/dissimilarities among the compounds. Stepwise regression models were calculated for each mobile phase modifier used. The obtained models were characterized by good fit and predictive abilities. The descriptors included in the models are connected with both lipophilic and donor/acceptor interactions.en
dc.publisherTaylor & Francis Inc, Philadelphia
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172013/RS//
dc.rightsrestrictedAccess
dc.sourceJournal of Liquid Chromatography & Related Technologies
dc.subjectMLRen
dc.subjectQSAR/QSRRen
dc.subjectPCAen
dc.subjectmolecular descriptorsen
dc.subjectinhibitory activityen
dc.subject5-arylidene-2,4-thiazolidinedionesen
dc.titleSubstituent effects on chromatographic retention data of 5-arylidene-2,4-thiazolidinediones in qsar methodologyen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage2035
dc.citation.issue14
dc.citation.other37(14): 2021-2035
dc.citation.rankM23
dc.citation.spage2021
dc.citation.volume37
dc.identifier.doi10.1080/10826076.2013.825858
dc.identifier.scopus2-s2.0-84898062058
dc.identifier.wos000334067600008
dc.type.versionpublishedVersion


Документи

Thumbnail

Овај документ се појављује у следећим колекцијама

Приказ основних података о документу