Pancreatic Lipase Inhibitory Cyclohexapeptides from the Marine Sponge-Derived Fungus Aspergillus sp. 151304

被引:21
|
作者
Tang, Wei-Zhuo [1 ,2 ]
Liu, Jing-Tang [2 ]
Hu, Qing [3 ]
He, Rong-Jing [3 ]
Guan, Xiao-Qing [3 ]
Ge, Guang-Bo [3 ]
Han, Hua [4 ]
Yang, Fan [2 ]
Lin, Hou-Wen [2 ]
机构
[1] Changsha Univ, Coll Biol & Environm Engn, Changsha 410022, Hunan, Peoples R China
[2] Shanghai Jiao Tong Univ, Renji Hosp, State Key Lab Oncogenes & Related Genes, Res Ctr Marine Drugs,Sch Med,Dept Pharm, Shanghai 200127, Peoples R China
[3] Shanghai Univ Tradit Chinese Med, Inst Interdisciplinary Integrat Med Res, Shanghai 201203, Peoples R China
[4] Tongji Univ, Sch Med, Shanghai 200092, Peoples R China
来源
JOURNAL OF NATURAL PRODUCTS | 2020年 / 83卷 / 07期
基金
中国国家自然科学基金;
关键词
CYCLIC-PEPTIDES; A-E; CYCLOPEPTIDES;
D O I
10.1021/acs.jnatprod.0c00549
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Three new cyclohexapeptides, petrosamides A-C (1-3), were isolated from the sponge-derived fungus Aspergillus sp. 151304. Their structures were elucidated by detailed 1D and 2D spectroscopic analyses, and the absolute configurations of the amino acid residues were determined by the advanced Marfey's method. These peptides displayed significant and dose-dependent pancreatic lipase (PL) inhibitory activities, with IC50 values of 7.6 +/- 1.5, 1.8 +/- 0.3, and 0.5 +/- 0.1 mu M, respectively. Further inhibition kinetics analyses showed that compound 3 inhibited PL in a noncompetitive manner, while molecular dynamics simulation revealed that it could bind to PL at the entrance of the catalytic pocket.
引用
收藏
页码:2287 / 2293
页数:7
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