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Cytotoxic effects of pyridino[2,3-f]indole-4,9-diones on human tumor cell lines.

Abstract
The cytotoxicities of pyridino[2,3-f]indole-4,9-dione derivatives were examined against human lung tumor cell lines (A 549), human ovarian tumor cell lines (SK-OV-3), human melanoma tumor cell lines (SK-MEL-2), human CNS tumor cell lines (XF 498) and human colon tumor cell lines (HCT 15) in vitro using a Sulforhodamine B assay. 3-Ethoxycarbonyl-1-(2-methoxyethyl)-2-methyl-1H-pyridino[2,3-f]ind ole-4,9-dione (5) showed excellent cytotoxicity against XF 498 and HCT 15. The ED50 values of 5 were 0.006 microg/ml against XF 498 and 0.073 microg/ml against HCT 15, while those of doxorubicin were 0.012 and 0.264 microg/ml, respectively. 1-Benzyl-3-ethoxycarbonyl-2-methyl-1H-pyridino[2,3-f]indole-4,9-di one (7) (ED50 value 0.065 microg/ml) was also significantly more cytotoxic against HCT 15 compared with doxorubicin.
AuthorsM E Suh, H K Park, H W Yoo, C O Lee
JournalBiological & pharmaceutical bulletin (Biol Pharm Bull) Vol. 23 Issue 3 Pg. 354-5 (Mar 2000) ISSN: 0918-6158 [Print] Japan
PMID10726894 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Indoles
  • Pyridines
Topics
  • Antineoplastic Agents (pharmacology)
  • Cell Division (drug effects)
  • Drug Screening Assays, Antitumor
  • Humans
  • Indoles (pharmacology)
  • Pyridines (pharmacology)
  • Tumor Cells, Cultured

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