Discovery of cycloheptapeptides phakefusins A-E from the marine sponge Phakellia fusca based on molecular networking

被引:0
|
作者
Wu, Ying [1 ]
Xu, Zhao-Ze [1 ]
Kong, Can [1 ]
Zhang, Shuai-Shuai [1 ]
Lin, Xin-Li [1 ]
Zhang, Si [1 ]
Liu, Li-Yun [1 ]
Sun, Fan [1 ]
Lin, Hou-Wen [1 ]
Wang, Shu-Ping [1 ]
机构
[1] Shanghai Jiao Tong Univ, Ren Ji Hosp, Marine Drug Integrated Innovat Ctr, Sch Med, Shanghai 200127, Peoples R China
基金
中国国家自然科学基金;
关键词
Phakellia fusca; Cyclopeptides; Structure elucidation; Molecular network; Cytotoxicity; Antioxidant activity; CONSTITUENT AMINO-ACIDS; ABSOLUTE-CONFIGURATION; MASS-SPECTROMETRY; MARFEYS METHOD; SEPARATION; LC/MS;
D O I
10.1016/j.phytochem.2024.114248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Guided by a probe-based molecular networking strategy, five undescribed cycloheptapeptides, phakefusins A-E (1-5), were isolated from the marine sponge Phakellia fusca. Compounds 1 and 2 contain the nonproteinogenic amino acid residues of dioxindolyalanine (Dioia) and beta-3-oxindolylalanine (Oia), respectively. Compound 3 possesses a unique methionine sulfoxide, whereas compound 5 includes a glutamic acid ethyl ester unit. Their structures were elucidated through NMR spectroscopy, HR-MS/MS analysis, and the advanced Marfey's method. By synthesizing the (S, S/R)-Oia standard through tryptophan oxidation, we determined the configuration of this amino acid in compound 2 using the advanced Marfey's method. These cycloheptapeptides were evaluated for their antitumor, antibacterial, and antioxidant activities. Compound 1 showed moderate cytotoxicity against MCF-7 and PC9 cells, with IC50 values of 6.8 and 9.6 mu M, respectively, while compounds 2-5 demonstrated potential antioxidant effects by upregulating HO-1, NQO1, and SOD2 levels, as well as inducing Nrf2 activation.
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页数:10
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