Microwave assisted synthesis and biomedical potency of salicyloyloxy and 2-methoxybenzoyloxy androstane and stigmastane derivatives

Steroids. 2015 Feb:94:31-40. doi: 10.1016/j.steroids.2014.12.008. Epub 2014 Dec 23.

Abstract

A convenient microwave assisted solvent free synthesis as well as conventional synthesis of salicyloyloxy and 2-methoxybenzoyloxy androstane and stigmastane derivatives 7-19 from appropriate steroidal precursors 1-6 and methyl salicylate is reported. The microwave assisted synthesis in most cases was more successful regarding reaction time and product yields. It was more environmentally friendly too, compared to the conventional method. The antioxidant activity and cytotoxicity of the synthesized derivatives were evaluated in a series of in vitro tests, as well as their inhibition potency exerted on hydroxysteroid dehydrogenase enzymes (Δ(5)-3βHSD, 17βHSD2 and 17βHSD3). All of the tested compounds were effective in OH radical neutralization, particularly compounds 9, 11 and 14, which exhibited about 100-fold stronger activity than commercial antioxidants BHT and BHA. In DPPH radical scavenging new compounds were effective, but less than reference compounds. 2-Methoxybenzoyl ester 10 exhibited strong cytotoxicity against MDA-MB-231 cells. Most compounds inhibited growth of PC-3 cells, where salicyloyloxy stigmastane derivative 15 showed the best inhibition potency. Compounds 9, 10 and 11 were the best inhibitors of 17βHSD2 enzyme. X-ray structure analysis and molecular mechanics calculations (MMC) were performed for the best cytotoxic agents, compounds 10 and 15. A comparison of crystal and MMC structures of compounds 10 and 15 revealed that their molecules conformations are stable even after releasing of the influence of crystalline field and that the influence of crystal packing on molecular conformation is not predominant.

Keywords: 17β-Hydroxysteroid dehydrogenase type 2 and type 3 (17βHSD2 and 3) inhibition; Antioxidant activity; Cytotoxicity; Steroidal salicylic acid derivatives; X-ray structural analysis; Δ(5)-3β-Hydroxysteroid dehydrogenase (Δ(5)-3βHSD) inhibition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Androstanes / chemical synthesis*
  • Androstanes / pharmacology
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Crystallography, X-Ray
  • Drug Screening Assays, Antitumor
  • Free Radical Scavengers / chemical synthesis*
  • Free Radical Scavengers / pharmacology
  • Humans
  • Hydroxybenzoate Ethers / chemical synthesis*
  • Hydroxybenzoate Ethers / pharmacology
  • Hydroxysteroid Dehydrogenases / antagonists & inhibitors
  • Inhibitory Concentration 50
  • Microwaves
  • Molecular Conformation
  • Salicylates / chemical synthesis*
  • Salicylates / pharmacology

Substances

  • Androstanes
  • Free Radical Scavengers
  • Hydroxybenzoate Ethers
  • Salicylates
  • Hydroxysteroid Dehydrogenases