Journal of the Brazilian Chemical Society (Jan 2003)

Synthesis and biological activity of three new 5a-hydroxy spirostanic brassinosteroid analogues

  • Rodríguez Caridad R.,
  • Villalobos Yohan I.,
  • Becerra Esther A.,
  • Manchado Francisco C.,
  • Herrera Deysma C.,
  • Zullo Marco A. T.

Journal volume & issue
Vol. 14, no. 3
pp. 466 – 469

Abstract

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Three new spirostanic brassinosteroid analogues have been synthesized for the first time from diosgenin: (25R)-2alpha,3alpha-epoxy-5alpha-hydroxyspirostan-6-one (3), (25R)-2beta,3alpha,5alpha-trihydroxyspirostan-6-one (5) and (25R)-2beta-methoxy-3alpha,5alpha-dihydroxyspirostan-6-one (6). In the radish hypocotyl elongation and cotyledon expansion bioassay compound 3 showed plant growth promoting activity whereas 6 was shown to be phytotoxic.

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