1996 Folia Pharm. Univ. Carol. 20 Pag. 63—66




Relationships between the Chemical Structure of Substances
and their Antimycobacterial Activity to Atypical Strains.

VIII. 2-Alkylthio-4-Pyridinecarbonitriles

Věra Klimešová1 (klimeso@faf.cuni.cz), Karel Waisser1, Vladimír Buchta2, Želmíra Odlerová3

1Department of Inorganic and Organic Chemistry, Faculty of Pharmacy, Charles University, Hradec Králové, Czech Republic
2Department of Biological and Medical Sciences, Faculty of Pharmacy, Charles University, Hradec Králové, Czech Republic
3Institute of Preventive and Clinical Medicine, Bratislava, Slovak Republic



Summary

2-Mercapto-4-pyridinecarbonitrile and a group of eleven 2-alkylthio-4-pyridinecarbonitriles were tested for their antimycobacterial activity against M. tuberculosis, M. kansasii, M. avium and M. fortuitum. The activity against M. fortuitum is very small. The activity of 2-mercapto-4-pyridinecarbonitrile and 2-hexylthio-4-pyridinecarbonitrile against atypical strains was higher than the activity of isoniazide and ethionamide.