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Dynemicins, new antibiotics with the 1,5-diyn-3-ene and anthraquinone subunit. II. Antitumor activity of dynemicin A and its triacetyl derivative.

Abstract
Dynemicin A showed extremely potent in vitro cytotoxicity against a variety of murine and human tumor cells. In the experimental animal tumor models implanted ip with P388, L1210 leukemias and B16 melanoma cells, dynemicin A administered ip significantly prolonged life-span of tumor-bearing mice with the wide range of activity. This antibiotic administered iv was also active against iv implanted P388 and L1210 leukemias. In the macromolecule biosynthesis of B16 melanoma cells, dynemicin A inhibited DNA synthesis specifically. The triacetyl derivative exhibited similar in vitro and in vivo antitumor activities to those of the parent antibiotic.
AuthorsH Kamei, Y Nishiyama, A Takahashi, Y Obi, T Oki
JournalThe Journal of antibiotics (J Antibiot (Tokyo)) Vol. 44 Issue 12 Pg. 1306-11 (Dec 1991) ISSN: 0021-8820 [Print] England
PMID1778783 (Publication Type: Journal Article)
Chemical References
  • Anthraquinones
  • Antibiotics, Antineoplastic
  • Enediynes
  • Nucleic Acids
  • dynemicin A
Topics
  • Animals
  • Anthraquinones (pharmacology, toxicity)
  • Antibiotics, Antineoplastic (pharmacology, toxicity)
  • DNA Damage
  • Enediynes
  • Humans
  • Lethal Dose 50
  • Male
  • Mice
  • Neoplasms, Experimental (drug therapy)
  • Nucleic Acids (biosynthesis)
  • Protein Biosynthesis
  • Tumor Cells, Cultured (drug effects)

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