Antifungal effects of new heterocyclic compounds, 6H-pyrimido[2,1-a]isoindole derivatives
Language English Country United States Media print
Document type Journal Article
PubMed
9569626
DOI
10.1007/bf02815539
Knihovny.cz E-resources
- MeSH
- Antifungal Agents pharmacology MeSH
- Heterocyclic Compounds, 4 or More Rings pharmacology MeSH
- Heterocyclic Compounds, 3-Ring pharmacology MeSH
- Indoles pharmacology MeSH
- Microbial Sensitivity Tests MeSH
- Pyrimidines pharmacology MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antifungal Agents MeSH
- Heterocyclic Compounds, 4 or More Rings MeSH
- Heterocyclic Compounds, 3-Ring MeSH
- Indoles MeSH
- Pyrimidines MeSH
Minimal inhibitory concentrations for 10 new condensed isoindole derivatives were established by the agar diffusion method. Benzo[b]-6H-pyrimido[2,1-a]isoindole-4-one exhibited a broad antifungal effect; the observed MIC (mg/L) were 7 (K. lactis), 8 (C. pseudotropicalis), 17 (W. fluorescens), 22 (E. magnusii), 31 (P. membranaefaciens), 32 (S. alluvius) and 32 (S. cerevisiae). The compound also inhibited the growth of B. subtilis (MIC 9 mg/L). No effect on the growth of E. coli was found.
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