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Cytotoxic activities of amino acid-conjugate derivatives of abietane-type diterpenoids against human cancer cell lines.

Abstract
Nine amino acid conjugate derivatives, each 2-10 and 12-20, were prepared from abietic acid (1) and dehydroabietic acid (11), respectively, and they were evaluated for their cytotoxicities against four human cancer cell lines, i.e., leukemia (HL60), lung (A549), stomach (AZ521), and breast (SK-BR-3). All compounds showed cytotoxicities against HL60 with IC50 values in the range of 2.3-37.3 μM. In addition, most of the derivatives exhibited moderate cytotoxicities against the other cancer cell lines. Among the derivatives, methyl N-[18-oxoabieta-8,11,13-trien-18-yl]-L-tyrosinate (19) exhibited potent cytotoxic activities against four cancer cell lines with IC50 values of 2.3 (HL60), 7.1 (A549), 3.9 (AZ521), and 8.1 μM (SK-BR-3). Furthermore, all derivatives were shown to possess high selective cytotoxic activities for leukemia cells, since they exhibited only weak cytotoxicities against normal lymphocyte cell line RPMI1788.
AuthorsMotohiko Ukiya, Takuma Kawaguchi, Kenta Ishii, Eri Ogihara, Yosuke Tachi, Masahiro Kurita, Yoichiro Ezaki, Makoto Fukatsu, Yasunori Kushi, Toshihiro Akihisa
JournalChemistry & biodiversity (Chem Biodivers) Vol. 10 Issue 7 Pg. 1260-8 (Jul 2013) ISSN: 1612-1880 [Electronic] Switzerland
PMID23847070 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich.
Chemical References
  • Abietanes
  • Amino Acids
  • Antineoplastic Agents
Topics
  • Abietanes (chemistry, toxicity)
  • Amino Acids (chemistry)
  • Antineoplastic Agents (chemical synthesis, chemistry, toxicity)
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Drug Screening Assays, Antitumor
  • HL-60 Cells
  • Humans

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