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Melanocins A, B and C, new melanin synthesis inhibitors produced by Eupenicillium shearii. I. Taxonomy, fermentation, isolation and biological properties.

Abstract
New melanin synthesis inhibitors, melanocins A, B and C, were isolated from the fermentation broth and mycelium extract of Eupenicillium shearii F80695. Melanocin A, an isocyanide compound, inhibited mushroom tyrosinase and melanin biosynthesis of B16 melanoma cells with IC50 value of 9.0 nM and MIC value of 0.9 microM, respectively. Melanocin A also inhibited growth of Streptomyces bikiniensis. While, the structurally very related but non-isocyanide compounds melanocins B and C did not show inhibitory activity in these assays. Melanocins A, B and C showed potent antioxidant activity with scavenging activity of DPPH radical and superoxide anion radical.
AuthorsJong-Pyung Kim, Byoung-Kwon Kim, Bong-Sik Yun, In-Ja Ryoo, Choong Hwan Lee, In-Kyoung Lee, Won-Gon Kim, Sangku Lee, Yu-Ryang Pyun, Ick-Dong Yoo
JournalThe Journal of antibiotics (J Antibiot (Tokyo)) Vol. 56 Issue 12 Pg. 993-9 (Dec 2003) ISSN: 0021-8820 [Print] England
PMID15015725 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Bacterial Agents
  • Butanones
  • Cyanides
  • Enzyme Inhibitors
  • Formamides
  • Free Radical Scavengers
  • Melanins
  • melanocin A
  • melanocin B
  • melanocin C
  • Monophenol Monooxygenase
Topics
  • Agaricales (enzymology)
  • Anti-Bacterial Agents (isolation & purification, pharmacology)
  • Ascomycota (classification, metabolism)
  • Butanones (isolation & purification, pharmacology)
  • Cyanides (isolation & purification, pharmacology)
  • Enzyme Inhibitors (isolation & purification, pharmacology)
  • Formamides (isolation & purification, pharmacology)
  • Free Radical Scavengers (isolation & purification, pharmacology)
  • Melanins (antagonists & inhibitors, biosynthesis)
  • Monophenol Monooxygenase (antagonists & inhibitors)
  • Streptomyces (drug effects, growth & development)

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