Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/13037
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dc.contributor.authorPoša, Mihaljen_US
dc.date.accessioned2020-03-03T14:50:46Z-
dc.date.available2020-03-03T14:50:46Z-
dc.date.issued2012-08-09-
dc.identifier.issn13852728en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/13037-
dc.description.abstractThe article is an extensive review of the influence of the structure of bile acids on their hydrophobicity as expressed via the retention parameters of reverse phase chromatography and via the 1-octanol/water partition coefficients. The emphasis of the discussion is on the relationship beween the structure of the steroid skeleton of bile acids and their self-association. Finally, the lipohilicity of bile acids and its role in their interaction with biological systems is also discussed. © 2012 Bentham Science Publishers.en
dc.relation.ispartofCurrent Organic Chemistryen
dc.titleHydrophobicity and self-association of bile acids with a special emphasis on oxo derivatives of 5-β cholanic aciden_US
dc.typeOtheren_US
dc.identifier.doi10.2174/138527212802651304-
dc.identifier.scopus2-s2.0-84864555947-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84864555947-
dc.description.versionUnknownen_US
dc.relation.lastpage1904en
dc.relation.firstpage1876en
dc.relation.issue16en
dc.relation.volume16en
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptMedicinski fakultet, Katedra za farmaciju-
crisitem.author.orcid0000-0002-8044-2655-
crisitem.author.parentorgMedicinski fakultet-
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