Natural Product Research · 2018 · 39 citations · 27 references
Life SciencesMedicinal ChemistryMicrobiologyBioorganic ChemistryMycologyOrganic ChemistryAromatic PlantsFungal Secondary MetabolitesMetabolite IdentificationStructure-activity Relationship AnalysisAntibacterial Spectrum Of ActivityBioactive Fungal MetabolitesEndophytic Fungal MetabolitesFungal Bioactive CompoundsPlant-associated Fungal MetabolitesStructure Elucidation Of Fungal Metabolites
A new xanthoquinodin B9 (1), together with two known xanthoquinodins, xanthoquinodin A1 (2) and xanthoquinodin A3 (3), three epipolythiodioxopiperazines, chetomin (4), chaetocochin C (5) and dethio-tetra(methylthio)chetomin (6), and four other compounds, chrysophanol (7), emodin (8), alatinone (9), and ergosterol (10) were isolated from the endophytic fungus Chaetomium globosum 7s-1, isolated from Rhapis cochinchinensis (Lour.) Mart. All isolated structures were established based on their spectroscopic data analyses. Compounds 1–6 showed antibacterial activity against Gram positive bacteria with MICs ranging from 0.02 pM to 10.81 µM. Compounds 1–6 also exhibited cytotoxicity against KB, MCF-7 and NCI-H187 cancer cell lines (IC50 0.04–18.40 µM). However, they were cytotoxic towards a normal cell line (Vero cell) with IC50 values ranging from 0.04 to 3.86 µM.
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Chaetocochins A−C, Epipolythiodioxopiperazines from <i>Chaetomium cochliode</i>s
Guo‐You Li, Bogang Li, Tao Yang et al. · Journal of Natural Products · 2006 · 75 citations
Life Sciences, Botany, Chemistry +7