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Cytotoxic Activities of Several Geranyl-Substituted Flavanones
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SYSNO ASEP 0349184 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Cytotoxic Activities of Several Geranyl-Substituted Flavanones Author(s) Šmejkal, K. (CZ)
Svačinová, Jana (UEB-Q)
Šlapetová, T. (CZ)
Schneiderová, K. (CZ)
Dall’Acqua, S. (IT)
Innocenti, G. (IT)
Závalová, V. (CZ)
Kollár, P. (SK)
Chudík, S. (CZ)
Marek, R. (CZ)
Julínek, O. (CZ)
Urbanová, M. (CZ)
Kartal, M. (HU)
Csöllei, M. (HU)
Doležal, Karel (UEB-Q) RID, ORCIDSource Title Journal of Natural Products. - : American Chemical Society - ISSN 0163-3864
Roč. 73, č. 4 (2010), s. 568-572Number of pages 5 s. Language eng - English Country US - United States Keywords flavanones ; geranyl ; cytotoxicity Subject RIV BO - Biophysics R&D Projects LC06030 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) GD522/08/H003 GA ČR - Czech Science Foundation (CSF) CEZ AV0Z50380511 - UEB-Q (2005-2011) UT WOS 000276950000011 DOI 10.1021/np900681y Annotation Nine geranylated flavanones isolatér from the fruits of Paulownia tomentosa and two from the roots of Morus alba were examinated for cytotoxicity to selected human cancor cell lines and normal human fibroblasts. Cytotoxicity was determined in vitro using a calcein AM cytotoxicity assay. Cytotoxicity for the THP-1 monocytic leukemia cell line was tested using erythrosin B cell staining. The geranylated compounds tested were compared with the known simple flavanone standards taxifolin (1), naringenin (2), and hesperetin (3), and with the standard anticancer druha olomoucine II, diaziquone and oxaliplatin and antineoplastic compound camptothecin, and showed different levels of cytotoxicity. The effect of structural changes on cytotoxic aktivity, including geranyl substitution of the flavanone skeleton and the oxidation pattern of ring B of the flavanones, are discussed. Workplace Institute of Experimental Botany Contact David Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469 Year of Publishing 2011
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