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• W2044294738 endingPage "2023" @default.
• W2044294738 startingPage "2019" @default.
• W2044294738 abstract "A new farnesyl hydroquinone, ganomycin I (1), was isolated along with ganomycin B (2) from the chloroform extract of the fruiting bodies of the Vietnamese mushroom Ganoderma colossum. These compounds inhibited HIV-1 protease with IC50 values of 7.5 and 1.0 μg/mL, respectively. Kinetic studies using Zhang−Poorman and Lineweaver plots revealed that compound 2 competitively inhibited the active site of the enzyme, whereas the tetracyclic triterpene schisanlactone A, previously isolated from the same fungus, was a dimerization inhibitor, with an IC50 value of 5.0 μg/mL. The previous findings were also confirmed by the virtual docking of both compounds with HIV-1 protease crystal structure." @default.
• W2044294738 created "2016-06-24" @default.
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• W2044294738 date "2009-10-08" @default.
• W2044294738 modified "2023-09-23" @default.
• W2044294738 title "Inhibition of the Dimerization and Active Site of HIV-1 Protease by Secondary Metabolites from the Vietnamese Mushroom <i>Ganoderma colossum</i>" @default.
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• W2044294738 doi "https://doi.org/10.1021/np900279u" @default.
• W2044294738 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19813754" @default.
• W2044294738 hasPublicationYear "2009" @default.
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