Reniochalistatins A-E, Cyclic Peptides from the Marine Sponge Reniochalina stalagmitis

被引:51
|
作者
Zhan, Kai-Xuan [1 ,3 ]
Jiao, Wei-Hua [2 ]
Yang, Fan [2 ]
Li, Jing [2 ]
Wang, Shu-Ping [2 ]
Li, Yu-Shan [1 ]
Han, Bing-Nan [2 ]
Lin, Hou-Wen [1 ,2 ,3 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Shenyang 110016, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, State Key Lab Oncogenes & Related Genes, Marine Drugs Res Ctr,Dept Pharm,Ren Ji Hosp, Shanghai 200127, Peoples R China
[3] Second Mil Med Univ, Changzheng Hosp, Dept Pharm, Shanghai 200003, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2014年 / 77卷 / 12期
基金
国家高技术研究发展计划(863计划);
关键词
TANDEM MASS-SPECTROMETRY; COLLISION-INDUCED DISSOCIATION; ANTINEOPLASTIC AGENTS; STYLISSA-CARIBICA; NATURAL-PRODUCTS; STYLOTELLA-AURANTIUM; PROTONATED PEPTIDES; PHAKELLIA SP; PROLINE; GROWTH;
D O I
10.1021/np5006778
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Five new cyclic peptides (including four heptapeptides and one octapeptide), reniochalistatins A-E (1-5), were isolated and characterized from the marine sponge Reniochalina stalagmitis collected off Yongxing Island in the South China Sea. Their structures were assigned on the basis of HRESIMS, 1D and 2D NMR spectroscopic data, and MALDI-TOF/TOF data for sequence analysis. The absolute configurations of all of the amino acid residues were determined using chiral-phase HPLC and Marfey's analysis. The cyclic octapeptide reniochalistatin E showed biological activity in various cytotoxicity assays employing different tumor cell lines (RPMI-8226, MGC-803, HL-60, HepG2, and HeLa). © 2014 The American Chemical Society and American Society of Pharmacognosy.
引用
收藏
页码:2678 / 2684
页数:7
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