1. University of Kragujevac Digital Archive
  2. University of Kragujevac
  3. Faculty of Science, Kragujevac
Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10201
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dc.rights.licenserestrictedAccess-
dc.contributor.authorJoksović, Milan-
dc.contributor.authorBogdanovic, Gordana-
dc.contributor.authorKojić, Vesna-
dc.contributor.authorMészáros Szécsényi, Katalin-
dc.contributor.authorLeovac V.-
dc.contributor.authorJakimov, Dimitar-
dc.contributor.authorTrifunović, Snežana-
dc.contributor.authorMarković, Violeta-
dc.contributor.authorJoksović, Ljubinka-
dc.date.accessioned2021-04-20T15:08:27Z-
dc.date.available2021-04-20T15:08:27Z-
dc.date.issued2010-
dc.identifier.issn0022-152X-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/10201-
dc.description.abstract(Chemical Equation Presented) New N-[(1,3-diphenylpyrazol-4-yl)methyl]a- 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. © 2010 HeteroCorporation.-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceJournal of Heterocyclic Chemistry-
dc.titleSynthesis, cytotoxic activity, and thermal studies of novel N-[(1,3-diphenylpyrazol-4-yl)methyl] α-amino acids-
dc.typearticle-
dc.identifier.doi10.1002/jhet.400-
dc.identifier.scopus2-s2.0-77954598700-
Appears in Collections:Faculty of Science, Kragujevac

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