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Eur J Med Chem ; 41(11): 1333-8, 2006 Nov.
Article in English | MEDLINE | ID: mdl-16889875

ABSTRACT

The synthesis and antimicrobial activity of isochromane-type analogs of the pyranonaphthoquinone antibiotics are reported. Isochromane derivatives with (17a, b) and without (22a, b) a C-4 hydroxyl moiety and their corresponding quinones (19a and 23), were prepared. Both quinones exhibited antimicrobial activity against Staphylococcus aureus, Bacillus atrophaeus and Streptococcus agalactiae, while the related isochromanes were inactive. The results suggest that the quinone moiety is important for biological activity while the C-4 hydroxyl may not be essential.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/pharmacology , Benzoquinones/chemical synthesis , Benzoquinones/pharmacology , Chromans/chemical synthesis , Anti-Bacterial Agents/chemistry , Benzoquinones/chemistry , Chromans/chemistry , Chromans/pharmacology , Magnetic Resonance Spectroscopy , Mass Spectrometry , Microbial Sensitivity Tests , Spectrophotometry, Infrared
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