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Synthesis, in vitro/in vivo antifungal evaluation and structure-activity relationship study of 3(2H)-pyridazinones.

Authors :
Károlyházy L
Freile M
Anwair MN
Beke G
Giannini F
Castelli MV
Sortino M
Ribas JC
Zacchino S
Mátyus P
Enriz RD
Source :
Arzneimittel-Forschung [Arzneimittelforschung] 2003; Vol. 53 (10), pp. 738-43.
Publication Year :
2003

Abstract

The synthesis, in vitro/in vivo antifungal evaluation and a structure-activity relationship (SAR) study of 3(2H)-pyridazinones was carried out. The results reported here may be helpful in the structural identification and understanding of the minimum structural requirements for these molecules acting as antifungal agents. In addition, the most active structure in this series was tested for its capacity of inhibiting Saccharomyces cerevisiae beta 1,3-glucan synthase and chitin synthase, enzymes that catalyze the synthesis of the major polymers of the fungal cell wall.

Details

Language :
English
ISSN :
0004-4172
Volume :
53
Issue :
10
Database :
MEDLINE
Journal :
Arzneimittel-Forschung
Publication Type :
Academic Journal
Accession number :
14650367
Full Text :
https://doi.org/10.1055/s-0031-1299820