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Cytotoxic xanthone-anthraquinone heterodimers from an unidentified fungus of the order Hypocreales (MSX 17022).


ABSTRACT: Two new xanthone-anthraquinone heterodimers, acremoxanthone C (5) and acremoxanthone D (2), have been isolated from an extract of an unidentified fungus of the order Hypocreales (MSX 17022) by bioactivity-directed fractionation as part of a search for anticancer leads from filamentous fungi. Two known related compounds, acremonidin A (4) and acremonidin C (3) were also isolated, as was a known benzophenone, moniliphenone (1). The structures of these isolates were determined via extensive use of spectroscopic and spectrometric tools in conjunction with comparisons to the literature. All compounds (1-5) were evaluated against a suite of biological assays, including those for cytotoxicity, inhibition of the 20S proteasome, mitochondrial transmembrane potential and nuclear factor-?B.

SUBMITTER: Ayers S 

PROVIDER: S-EPMC3267898 | biostudies-literature | 2012 Jan

REPOSITORIES: biostudies-literature

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Cytotoxic xanthone-anthraquinone heterodimers from an unidentified fungus of the order Hypocreales (MSX 17022).

Ayers Sloan S   Graf Tyler N TN   Adcock Audrey F AF   Kroll David J DJ   Shen Qi Q   Swanson Steven M SM   Matthew Susan S   Carcache de Blanco Esperanza J EJ   Wani Mansukh C MC   Darveaux Blaise A BA   Pearce Cedric J CJ   Oberlies Nicholas H NH  

The Journal of antibiotics 20111109 1


Two new xanthone-anthraquinone heterodimers, acremoxanthone C (5) and acremoxanthone D (2), have been isolated from an extract of an unidentified fungus of the order Hypocreales (MSX 17022) by bioactivity-directed fractionation as part of a search for anticancer leads from filamentous fungi. Two known related compounds, acremonidin A (4) and acremonidin C (3) were also isolated, as was a known benzophenone, moniliphenone (1). The structures of these isolates were determined via extensive use of  ...[more]

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