4.7 Article

Trichormamides A and B with Antiproliferative Activity from the Cultured Freshwater Cyanobacterium Trichormus sp UIC 10339

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JOURNAL OF NATURAL PRODUCTS
卷 77, 期 8, 页码 1871-1880

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AMER CHEMICAL SOC
DOI: 10.1021/np5003548

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  1. NCI/NIH [PO1 CA125066]
  2. NIH [GM068944]

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Two new cyclic lipopeptides, trichormamides A (1) and B (2), were isolated from the cultured freshwater cyanobacterium Trichormus sp. UIC 10339. The strain was obtained from a sample collected in Raven Lake in Northern Wisconsin. The planar structures of trichormamides A (1) and B (2) were determined using a combination of spectroscopic analyses including HRESIMS and 1D and 2D NMR experiments. The absolute configurations of the amino acid residues were assigned by the advanced Marfey's method after acid hydrolysis. Trichormamide A (1) is a cyclic undecapeptide containing two D-amino acid residues (D-Tyr and D-Leu) and one beta-amino acid residue (beta-aminodecanoic acid). Trichormamide B (2) is a cyclic dodecapeptide characterized by the presence of four nonstandard alpha-amino acid residues (homoserine, N-methylisoleucine, and two 3-hydroxyleucines) and one beta-amino acid residue (beta-aminodecanoic acid). Trichormamide B (2) was cytotoxic against MDA-MB-435 and HT-29 cancer cell lines with IC50 values of 0.8 and 1.5 mu M, respectively.

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