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

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Abstract

Three new spirostanic brassinosteroid analogues have been synthesized for the first time from diosgenin: (25R)-2α,3α-epoxy-5α-hydroxyspirostan-6-one (3), (25R)-2β,3α,5α-trihydroxyspirostan-6-one (5) and (25R)-2β-methoxy-3α,5α-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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APA

Rodríguez, C. R., Villalobos, Y. I., Becerra, E. A., Manchado, F. C., Herrera, D. C., & Zullo, M. A. T. (2003). Synthesis and biological activity of three new 5α-hydroxy spirostanic brassinosteroid analogues. Journal of the Brazilian Chemical Society, 14(3), 466–469. https://doi.org/10.1590/S0103-50532003000300022

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