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A bioactive seco-rosane diterpenoid from Vellozia candida.

Abstract
Bioassay-directed fractionation of the bioactive alcoholic extracts of Vellozia candida yielded a new 6,7-seco-rosane diterpenoid, candidalactone (1), which showed moderate toxicity toward DNA repair-deficient mutants of Saccharomyces cerevisiae. Another new but inactive rosane diterpenoid, candidenodiol (3), was also obtained.
AuthorsL M Valente, A A Gunatilaka, D G Kingston, M L Patitucci, A C Pinto
JournalJournal of natural products (J Nat Prod) Vol. 60 Issue 5 Pg. 478-81 (May 1997) ISSN: 0163-3864 [Print] United States
PMID9170291 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antimutagenic Agents
  • Coumarins
  • Diterpenes
  • candidalactone
Topics
  • Antimutagenic Agents (isolation & purification, pharmacology)
  • Coumarins (isolation & purification, pharmacology)
  • DNA Repair
  • Diterpenes (isolation & purification, pharmacology)
  • Magnetic Resonance Spectroscopy
  • Plants, Medicinal (chemistry)
  • Saccharomyces cerevisiae (drug effects, genetics)
  • Spectrophotometry, Infrared
  • Spectrophotometry, Ultraviolet

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