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Effect of benfluron metabolites on ATP level in tumor cells.

Abstract
Changes in ATP levels of both Ehrlich ascites carcinoma and P388 leukemia cells were evaluated after 2 h of incubation in the presence of different concentrations of benfluron (BF), 7-dihydrobenfluron (DBF) and N-oxide of benfluron (NOBF). Up to the concentration of 37.5 mumol/l, none of the substances significantly depressed the ATP levels. A more expressive decrease in ATP levels was noted only at concentrations of 75 mumol/l and higher. BF proved the most effective, less effective was DBF, while NOBF was practically without any effect. Of the remaining cytostatic drugs, Mitoxantrone, CCNU and Me-CCNU, in particular, proved efficient in depressing ATP level. The latter becomes depressed already after 15 min of incubation in the presence of the highest concentrations of benfluron and 7-dihydrobenfluron.
AuthorsM Miko, J Krepelka, M Mĕlka, D Vajdová
JournalNeoplasma (Neoplasma) Vol. 36 Issue 4 Pg. 411-7 ( 1989) ISSN: 0028-2685 [Print] Slovakia
PMID2770928 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Antineoplastic Agents
  • Fluorenes
  • VUFB 13468
  • 7-dihydrobenfluron
  • Adenosine Triphosphate
  • benfluron N-oxide
Topics
  • Adenosine Triphosphate (metabolism)
  • Animals
  • Antineoplastic Agents (pharmacology)
  • Carcinoma, Ehrlich Tumor (metabolism)
  • Fluorenes (pharmacology)
  • Kinetics
  • Leukemia P388 (metabolism)
  • Leukemia, Experimental (metabolism)
  • Mice

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