Affiliation:
1. Department of Biochemical Engineering, Graduate School of Science and Technology, Yamagata University, Yonezawa, Japan
Abstract
Abstract
The cytotoxic evaluation of natural and synthetic callipeltins is described. Cyclic depsipeptide callipeltin B and linear peptides callipeltins E and M synthesized by us showed no cytotoxic activity. In contrast, natural callipeltin B purified from Callipelta sp. showed CC50 = 130 μM against Hela cells. We found that purified callipeltin B included the contamination of callipeltins C and H at a ratio of approximately 15%. These results suggested that the cytotoxicity of natural callipeltin B was derived from callipeltins C and H.
Publisher
Oxford University Press (OUP)
Subject
Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology
Reference19 articles.
1. Callipeltin A, an anti-HIV cyclic depsipeptide from the New Caledonian lithistida sponge Callipelta sp;Zampella;J. Am. Chem. Soc,1996
2. Homophymine A, an Anti-HIV cyclodepsipeptide from the sponge Homophymia sp;Zampella;J. Org. Chem,2008
3. Homophymines B-E and A1-E1, a family of bioactive cyclodepsipeptides from the sponge Homophymia sp;Zampella;Org. Biomol. Chem,2009
4. Papuamides A−D, HIV-inhibitory and cytotoxic depsipeptides from the sponges Theonella mirabilis and Theonella swinhoei collected in Papua New Guinea;Ford;J. Am. Chem. Soc,1999
5. Papuamides E and F, cytotoxic depsipeptides from the marine sponge Melophlus sp;Prasad;Tetrahedron,2011
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