4.7 Article

Tolypocladamides A-G: Cytotoxic Peptaibols from Tolypocladium inflatum

期刊

JOURNAL OF NATURAL PRODUCTS
卷 85, 期 6, 页码 1603-1616

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AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.2c00240

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资金

  1. Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research [1ZIABC 011470-10, 1ZIABC010329-22]
  2. National Cancer Institute, National Institutes of Health [HHSN261200800001E]
  3. National Institute of General Medical Sciences of the National Institutes of Health [R01GM092219]

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Seven new peptaibols were isolated from the fungus Tolypocladium inflatum, which showed inhibitory effects on the interaction between Raf and oncogenic Ras. The structures and activities of the peptaibols were determined using various analytical methods. However, these peptaibols exhibited low selectivity in different cell lines.
Seven new peptaibols named tolypocladamides A-G have been isolated from an extract of the fungus Tolypocladium inflatum, which inhibits the interaction between Raf and oncogenic Ras in a cell-based high-throughput screening assay. Each peptaibol contains 11 amino acid residues, an octanoyl or decanoyl fatty acid chain at the N-terminus, and a leucinol moiety at the C-terminus. The peptaibol sequences were elucidated on the basis of 2D NMR and mass spectral fragmentation analyses. Amino acid configurations were determined by advanced Marfey's analyses. Tolypocladamides A-G caused significant inhibition of Ras/Raf interactions with IC50 values ranging from 0.5 to 5.0 mu M in a nanobioluminescence resonance energy transfer (NanoBRET) assay; however, no interactions were observed in a surface plasmon resonance assay for binding of the compounds to wild type or G12D mutant Ras constructs or to the Ras binding domain of Raf. NCI 60 cell line testing was also conducted, and little panel selectivity was observed.

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