Rational design of 5'-thiourea-substituted alpha-thymidine analogues as thymidine monophosphate kinase inhibitors capable of inhibiting mycobacterial growth

J Med Chem. 2007 Nov 1;50(22):5281-92. doi: 10.1021/jm0706158. Epub 2007 Oct 2.

Abstract

Recently, thymidine monophosphate kinase (TMPK) emerged as an attractive target for developing inhibitors of Mycobacterium tuberculosis growth. The elucidation of the X-ray structure of TMPK of M. tuberculosis (TMPKmt), as well as the structure of an earlier serendipitously discovered dimeric thymidine inhibitor, laid the foundation for the design of potent and selective TMPKmt inhibitors reported here. Several hits identified within a series of 3'-C-branched thiourea-substituted beta-thymidine derivatives inspired us to construct a set of 5'-thiourea-substituted alpha-thymidine derivatives characterized by a similar relative orientation of the thymine and arylthiourea moieties. alpha-Thymidine derivative 15, featuring a (3-trifluoromethyl-4-chlorophenyl)thiourea moiety, has a Ki of 0.6 microM and a selectivity index of 600 versus human TMPK. Moreover, it represents the first TMPK inhibitor showing good inhibitory activity on growing M. bovis (MIC99 = 20 microg/mL) and M. tuberculosis (MIC50 = 6.25 microg/mL) strains.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / chemical synthesis*
  • Anti-Bacterial Agents / pharmacology
  • Chlorocebus aethiops
  • Crystallography, X-Ray
  • Dimerization
  • Humans
  • Models, Molecular
  • Mycobacterium / drug effects*
  • Mycobacterium / enzymology
  • Mycobacterium / growth & development
  • Mycobacterium bovis / drug effects
  • Mycobacterium bovis / enzymology
  • Mycobacterium bovis / growth & development
  • Mycobacterium tuberculosis / drug effects
  • Mycobacterium tuberculosis / enzymology
  • Mycobacterium tuberculosis / growth & development
  • Nucleoside-Phosphate Kinase / antagonists & inhibitors*
  • Nucleoside-Phosphate Kinase / chemistry
  • Nucleosides / chemical synthesis*
  • Nucleosides / pharmacology
  • Stereoisomerism
  • Structure-Activity Relationship
  • Thiourea / analogs & derivatives*
  • Thiourea / chemical synthesis*
  • Thiourea / pharmacology
  • Thymidine / analogs & derivatives*
  • Thymidine / chemical synthesis*
  • Thymidine / pharmacology
  • Vero Cells

Substances

  • Anti-Bacterial Agents
  • Nucleosides
  • Nucleoside-Phosphate Kinase
  • dTMP kinase
  • Thiourea
  • Thymidine