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Bioorg Med Chem Lett ; 37: 127845, 2021 04 01.
Article in English | MEDLINE | ID: mdl-33571649

ABSTRACT

Thirty-five pyridone derivatives were synthesized, with derivatization conducted on polycyclic pyridone scaffolds, including cis- or trans-oxydecalin and other cyclic structures, by domino-Knoevenagel-electrocyclic reactions. The anti-fungal activities of the synthesized compounds were tested against Candida albicans. Ten compounds inhibited hyphal formation without inhibiting growth. Pyridones with anti-hyphal formation activity (4c, 6d, 12a and 12c) were tested for their ability to inhibit biofilm formation. Compound 6d showed both anti-hyphal and biofilm inhibition activity.


Subject(s)
Antifungal Agents/pharmacology , Candida albicans/drug effects , Heterocyclic Compounds/pharmacology , Pyridones/pharmacology , Antifungal Agents/chemical synthesis , Antifungal Agents/chemistry , Biofilms/drug effects , Dose-Response Relationship, Drug , Heterocyclic Compounds/chemical synthesis , Heterocyclic Compounds/chemistry , Microbial Sensitivity Tests , Molecular Structure , Pyridones/chemical synthesis , Pyridones/chemistry , Structure-Activity Relationship
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