期刊
JOURNAL OF NATURAL PRODUCTS
卷 80, 期 6, 页码 1948-1952出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.7b00256
关键词
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资金
- JSPS KAKENHI Grant [16K13091]
- Grants-in-Aid for Scientific Research [16K13091] Funding Source: KAKEN
Kohamamides A, B, and C (13), new cyclic depsipeptides that belong to the kulolide superfamily, were isolated from an Okeania sp. marine cyanobacterium. Their structures were elucidated by spectroscopic analyses and degradation reactions. Kohamamide B (2) exhibited moderate cytotoxicity against HL60 cells. Although many natural products in the kulolide superfamily have been isolated from cyanobacteria collected in various parts of the world, kohamamides 13 are the first members to be isolated from the East Asian marine environment. In addition, unlike other members of this superfamily, kohamamides 13 contain a Leu residue adjacent to the Pro residue, rather than another lipophilic amino acid.
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