Synthesis of novel aryl brassinosteroids through alkene cross-metathesis and preliminary biological study

Steroids. 2017 Nov:127:46-55. doi: 10.1016/j.steroids.2017.08.010. Epub 2017 Aug 31.

Abstract

A series of phenyl analogues of brassinosteroids was prepared via alkene cross-metathesis using commercially available styrenes and 24-nor-5α-chola-2,22-dien-6-one. All derivatives were successfully docked into the active site of BRI1 using AutoDock Vina. Plant growth promoting activity was measured using the pea inhibition biotest and Arabidopsis root sensitivity assay and then was compared with naturally occuring brassinosteroids. Differences in the production of plant hormone ethylene were also observed in etiolated pea seedlings after treatment with the new and also five known brassinosteroid phenyl analogues. Antiproliferative activity was also studied using normal human fibroblast and human cancer cell lines.

Keywords: BRI1 receptor kinase; Brassinosteroids; Cross-metathesis; Molecular docking; Organic synthesis; Plant bioassays.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Arabidopsis / drug effects
  • Arabidopsis / enzymology
  • Arabidopsis / growth & development
  • Arabidopsis Proteins / chemistry
  • Arabidopsis Proteins / metabolism
  • Brassinosteroids / chemical synthesis*
  • Brassinosteroids / chemistry
  • Brassinosteroids / metabolism
  • Brassinosteroids / pharmacology*
  • Catalytic Domain
  • Chemistry Techniques, Synthetic
  • Molecular Docking Simulation
  • Pisum sativum / drug effects
  • Pisum sativum / growth & development
  • Protein Kinases / chemistry
  • Protein Kinases / metabolism

Substances

  • Alkenes
  • Arabidopsis Proteins
  • Brassinosteroids
  • Protein Kinases
  • BRI1 protein, Arabidopsis