Synthesis and antiproliferative activity of pterostilbene and 3′-methoxy pterostilbene Mannich base derivatives against Hela cells

Mol Divers. 2015 Nov;19(4):737-43. doi: 10.1007/s11030-015-9615-1. Epub 2015 Jul 11.

Abstract

Fourteen novel pterostilbene (1) and [Formula: see text]-methoxy pterostilbene (2) Mannich base derivatives (3-16) were synthesized via the microwave-assisted Mannich reaction of 1 or 2 with various secondary amines and formaldehyde. The regioselectivity of the reaction occurred preferentially at [Formula: see text] position of the B-ring of stilbene. The biological testing results showed that all the target compounds exhibit antiproliferative activity against Hela cells from [Formula: see text]-[Formula: see text]. Compounds 1-3, 7, 11-13, and 16 displayed higher (lower [Formula: see text] values) activity than the positive control cisplatin [Formula: see text].

Keywords: -Methoxy pterostilbene; Antiproliferative activity; Hela cells; Mannich base derivatives; Pterostilbene; Synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Cell Proliferation / drug effects
  • HeLa Cells
  • Humans
  • Mannich Bases
  • Molecular Structure
  • Stilbenes / chemical synthesis*
  • Stilbenes / pharmacology*

Substances

  • Antineoplastic Agents
  • Mannich Bases
  • Stilbenes
  • pterostilbene