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dc.contributor.authorZloh, Mire
dc.contributor.authorGibbons, S.
dc.date.accessioned2014-01-08T16:30:37Z
dc.date.available2014-01-08T16:30:37Z
dc.date.issued2004-02-01
dc.identifier.citationZloh , M & Gibbons , S 2004 , ' Molecular similarity of MDR inhibitors ' , International Journal of Molecular Sciences , vol. 5 , no. 2 , pp. 37-47 . https://doi.org/10.3390/i5020037
dc.identifier.issn1422-0067
dc.identifier.otherPURE: 1448039
dc.identifier.otherPURE UUID: fae15539-fdf4-47b0-b792-a9d0ff811fa6
dc.identifier.otherScopus: 2942609006
dc.identifier.urihttp://hdl.handle.net/2299/12485
dc.descriptionEveryone is free to re-use the published material if proper accreditation/citation of the original publication is given. http://creativecommons.org/licences/by/3.0/
dc.description.abstractThe molecular similarity of multidrug resistance (MDR) inhibitors was evaluated using the point centred atom charge approach in an attempt to find some common features of structurally unrelated inhibitors. A series of inhibitors of bacterial MDR were studied and there is a high similarity between these in terms of their shape, presence and orientation of aromatic ring moieties. A comparison of the lipophilic properties of these molecules has also been conducted suggesting that this factor is important in MDR inhibition.en
dc.format.extent11
dc.language.isoeng
dc.relation.ispartofInternational Journal of Molecular Sciences
dc.titleMolecular similarity of MDR inhibitorsen
dc.contributor.institutionDepartment of Pharmacy
dc.contributor.institutionMedicinal and Analytical Chemistry
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionHealth & Human Sciences Research Institute
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=2942609006&partnerID=8YFLogxK
rioxxterms.versionVoR
rioxxterms.versionofrecordhttps://doi.org/10.3390/i5020037
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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