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dc.creatorDobričić, Vladimir
dc.creatorVladimirov, Sote
dc.creatorČudina, Olivera
dc.date.accessioned2019-09-02T11:50:36Z
dc.date.available2019-09-02T11:50:36Z
dc.date.issued2016
dc.identifier.issn1450-9636
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/2537
dc.description.abstractCortienic acid was obtained by periodic acid oxidation of fluocinolone acetonide, whereas corresponding amide was synthesized from the cortienic acid and ethyl ester of b-alanine by dicyclohexylcarbodiimide - hydroxybenzotriazole coupling procedure. Lipophilicity of the amide was evaluated by using reversed-phase thin-layer chromatography systems, consisting of ethanol and water in various ratios, and was higher in comparison to fluocinolone acetonide and cortienic acid.en
dc.publisherUniverzitet u Kragujevcu - Prirodno-matematički fakultet, Kragujevac
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172041/RS//
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceKragujevac Journal of Science
dc.subjectcortienic aciden
dc.subjectamideen
dc.subjectlipophilicityen
dc.subjectRP-TLCen
dc.titleSynthesis and RP-TLC lipophilicity evaluation of a novel fluocinolon acetonide soft drug derivativeen
dc.typearticle
dc.rights.licenseBY
dcterms.abstractДобричић, Владимир; Владимиров, Соте; Чудина, Оливера;
dc.citation.issue38
dc.citation.spage107
dc.citation.epage114
dc.citation.other(38): 107-114
dc.citation.rankM51
dc.identifier.doi10.5937/KgJSci1638107D
dc.identifier.fulltexthttps://farfar.pharmacy.bg.ac.rs//bitstream/id/1211/2535.pdf
dc.type.versionpublishedVersion


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Приказ основних података о документу