Synthesis and biological evaluation against Mycobacterium tuberculosis and Leishmania amazonensis of a series of diaminated terpenoids

Biomed Pharmacother. 2016 Dec:84:1739-1747. doi: 10.1016/j.biopha.2016.10.112. Epub 2016 Nov 18.

Abstract

We report the synthesis of a series of diaminated terpenoids containing, as side-chain of the diamine core, the "head-to-tail" prenyl derivatives, with amino amino spacers of variable length. In vitro biological activity of these compounds was evaluated against Mycobacterium tuberculosis and Leishmania amazonensis, and the structure-activity relationships are discussed. Different biological results were observed depending on the terpenic side-chain length. The best results were obtained for trans,trans-farnesol derivatives. Moreover, these results demonstrated that the stereochemistry of the double bond could play an important role in determining antitubercular and antileishmanial activities of these compounds.

Keywords: Diamine; Leishmaniasis; Terpenoid; Tuberculosis.

MeSH terms

  • Antiprotozoal Agents / chemical synthesis*
  • Antiprotozoal Agents / pharmacology*
  • Antitubercular Agents / chemical synthesis*
  • Antitubercular Agents / pharmacology*
  • Diamines / chemical synthesis*
  • Diamines / pharmacology*
  • Drug Design
  • Leishmania mexicana / drug effects*
  • Leishmania mexicana / growth & development
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Mycobacterium tuberculosis / drug effects*
  • Mycobacterium tuberculosis / growth & development
  • Parasitic Sensitivity Tests
  • Structure-Activity Relationship
  • Terpenes / chemical synthesis*
  • Terpenes / pharmacology*

Substances

  • Antiprotozoal Agents
  • Antitubercular Agents
  • Diamines
  • Terpenes