1996 Folia Pharm. Univ. Carol. 20 Pag. 31—34




Relations Quantitatives Entre Structure Chimique et Hépatotoxicité des Dithiooxalamides

Karel Waisser1 (waisser@faf.cuni.cz), Nestor Houngbedji1, Jaroslav Dršata1, Wilfried Thiel2, Roland Mayer3

1Faculté de Pharmacie, Université Charles, Hradec Králové, République Tchéque
2Arzneimittelwerk Dresden, Radebeul, Allemagne
3Université Technique Dresden, Allemagne



English Summary

Quantitative Chemical Structure—Hepatotoxicity Relationship of Dithiooxalamides

In a group of antituberculously effective derivatives of dithiooxalamide studied with a prospect of the develepment of novel antituberculous agents, hepatotoxity was found to correlate with the values of RM from chromatography an thin layers of octadecylsilanized silica gel. Hepatotoxicity was evaluated by the activity of alaninamino transferase in blood serum.