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dc.creatorJoksović, Milan D.
dc.creatorBogdanović, Gordana
dc.creatorKojic, Vesna
dc.creatorSzecsenyi, Katalin Meszaros
dc.creatorLeovac, Vukadin M.
dc.creatorJakimov, Dimitar
dc.creatorTrifunović, Snežana S.
dc.creatorMarković, Violeta
dc.creatorJoksović, Ljubinka
dc.date.accessioned2018-11-22T00:16:41Z
dc.date.available2018-11-22T00:16:41Z
dc.date.issued2010
dc.identifier.issn0022-152X
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/1097
dc.description.abstractNew N-[(1,3-diphenylpyrazol-4-yl)methyl]alpha-amino acids (1a-i) have been synthesized and tested in vitro for their antiproliferative activity against human myelogenous leukemia K562, colon adenocarcinoma HT-29, cervix carcinoma HeLa, and normal fetal lung fibroblasts, MRC-5. Compounds derived from both phenylalanine enantiomer precursors appeared to be the most active against myelogenous leukemia K562 cell lines with a high cytotoxic potential.en
dc.publisherWiley-Blackwell, Malden
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142028/RS//
dc.relationProvincial Secretariat for Science and Technological Development of Vojvodina
dc.rightsrestrictedAccess
dc.sourceJournal of Heterocyclic Chemistry
dc.titleSynthesis, Cytotoxic Activity, and Thermal Studies of Novel N-[(1,3-Diphenylpyrazol-4-yl)methyl] alpha-Amino Acidsen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractЈоксовиц, Љубинка; Сзецсенyи, Каталин Месзарос; Трифуновић, Снежана; Марковиц, Виолета; Леовац, Вукадин М.; Јоксовиц, Милан Д.; Јакимов, Димитар; Којиц, Весна; Богдановиц, Гордана;
dc.citation.volume47
dc.citation.issue4
dc.citation.spage850
dc.citation.epage856
dc.identifier.wos000280450700010
dc.identifier.doi10.1002/jhet.400
dc.citation.other47(4): 850-856
dc.citation.rankM23
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-77954598700
dc.identifier.rcubKon_2097


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