Highly active antimycobacterial derivatives of benzoxazine

Bioorg Med Chem. 2010 Dec 1;18(23):8178-87. doi: 10.1016/j.bmc.2010.10.017. Epub 2010 Oct 19.

Abstract

New 3-(4-alkylphenyl)-4-thioxo-2H-1,3-benzoxazine-2(3H)-ones and 3-(4-alkylphenyl)-2H-1,3-benzoxazine-2,4(3H)-dithiones were synthesized. The compounds were tested for in vitro antimycobacterial activity against Mycobacterium tuberculosis, Mycobacterium avium and two strains of Mycobacterium kansasii. The antimycobacterial activity increased with the replacement of the carbonyl group by the thiocarbonyl group in the starting 3-(4-alkylphenyl)-2H-1,3-benzoxazine-2,4(3H)-diones. The most active derivatives were more active than isonicotinhydrazide (INH). Free-Wilson analysis was also carried out and the activity contribution was examined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antitubercular Agents / chemical synthesis
  • Antitubercular Agents / chemistry*
  • Antitubercular Agents / pharmacology
  • Benzoxazines / chemical synthesis
  • Benzoxazines / chemistry*
  • Benzoxazines / pharmacology
  • Isoniazid / pharmacology
  • Microbial Sensitivity Tests
  • Mycobacterium avium / drug effects*
  • Mycobacterium kansasii / drug effects*
  • Mycobacterium tuberculosis / drug effects*
  • Structure-Activity Relationship

Substances

  • Antitubercular Agents
  • Benzoxazines
  • Isoniazid