Antifungal properties of a novel 1,2,4-triazine derivative I 319.

Abstract

The antifungal activity of the sodium salts, of 3-thiolo-5-phenyl-1,2,4-triazine (I 319) was determined in vitro and in vivo. The minimal inhibitory concentration (MIC) of I 319 for 33 pathogenic and saprophytic fungal strains ranged from 3.1 to 25 microgram/ml. In vivo, experiments were performed on a model of subacute candidiasis in Balb/c mice infected intraperitoneally with Candida albicans. The antifungal activity was estimated on the basis of the extension of the mice life span and on the number of living yeast cells present in the kidneys, liver and spleen of treated and control mice. A single i.p. dose of I 319 (25 mg/kg) prolonged the survival time of treated animals up to 200%. Five subsequent doses of the compound diminished the number of C. albicans cells in the tissues of these mice. The DL50 of I 319 for mice (i.p.) was about 250 mg/kg.

• Authors: J Wieczorek, M Mordarski, A Rykowski, P Nantka-Namirski
• Journal: Archivum immunologiae et therapiae experimentalis (Arch Immunol Ther Exp (Warsz)) Vol. 28 Issue 5 Pg. 727-33 ( 1980) ISSN: 0004-069X [Print] Switzerland
• PMID: 7212980 (Publication Type: Comparative Study, Journal Article)

Chemical References

• Antifungal Agents
• Triazines
• I 319

Topics

• Animals
• Antifungal Agents
• Candidiasis (drug therapy, mortality)
• Chemical Phenomena
• Chemistry
• Dose-Response Relationship, Drug
• Drug Evaluation, Preclinical
• In Vitro Techniques
• Male
• Mice
• Time Factors
• Triazines (administration & dosage, pharmacology, therapeutic use)