Synthesis and Leishmanicidal Activity of Novel Urea, Thiourea, and Selenourea Derivatives of Diselenides

Antimicrob Agents Chemother. 2019 Apr 25;63(5):e02200-18. doi: 10.1128/AAC.02200-18. Print 2019 May.

Abstract

A novel series of thirty-one N-substituted urea, thiourea, and selenourea derivatives containing diphenyldiselenide entities were synthesized, fully characterized by spectroscopic and analytical methods, and screened for their in vitro leishmanicidal activities. The cytotoxic activity of these derivatives was tested against Leishmania infantum axenic amastigotes, and selectivity was assessed in human THP-1 cells. Thirteen of the synthesized compounds showed a significant antileishmanial activity, with 50% effective concentration (EC50) values lower than that for the reference drug miltefosine (EC50, 2.84 μM). In addition, the derivatives 9, 11, 42, and 47, with EC50 between 1.1 and 1.95 μM, also displayed excellent selectivity (selectivity index ranged from 12.4 to 22.7) and were tested against infected macrophages. Compound 11, a derivative with a cyclohexyl chain, exhibited the highest activity against intracellular amastigotes, with EC50 values similar to those observed for the standard drug edelfosine. Structure-activity relationship analyses revealed that N-aliphatic substitution in urea and selenourea is recommended for the leishmanicidal activity of these analogs. Preliminary studies of the mechanism of action for the hit compounds was carried out by measuring their ability to inhibit trypanothione reductase. Even though the obtained results suggest that this enzyme is not the target for most of these derivatives, their activity comparable to that of the standards and lack of toxicity in THP-1 cells highlight the potential of these compounds to be optimized for leishmaniasis treatment.

Keywords: selenium; selenourea; thiourea; trypanothione reductase; urea.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiprotozoal Agents / chemical synthesis*
  • Antiprotozoal Agents / chemistry
  • Antiprotozoal Agents / therapeutic use*
  • Humans
  • Leishmania infantum / drug effects*
  • Leishmania infantum / pathogenicity
  • Macrophages / parasitology
  • NADH, NADPH Oxidoreductases / metabolism
  • Organoselenium Compounds / chemistry*
  • Parasitic Sensitivity Tests
  • Structure-Activity Relationship
  • Thiourea / chemistry*
  • Urea / analogs & derivatives*
  • Urea / chemistry*

Substances

  • Antiprotozoal Agents
  • Organoselenium Compounds
  • selenourea
  • Urea
  • NADH, NADPH Oxidoreductases
  • trypanothione reductase
  • Thiourea