Natural soluble epoxide hydrolase inhibitors from Alisma orientale and their potential mechanism with soluble epoxide hydrolase

被引:19
|
作者
Zhao, Wen-Yu [1 ]
Zhang, Xin-Yue [1 ]
Zhou, Mei-Rong [1 ]
Tian, Xiang-Ge [1 ]
Lv, Xia [1 ]
Zhang, Hou-Li [1 ]
Deng, Sa [1 ]
Zhang, Bao-Jing [1 ]
Sun, Cheng-Peng [1 ]
Ma, Xiao-Chi [1 ,2 ]
机构
[1] Dalian Med Univ, Coll Pharm, Coll Inst Integrat Med, Dalian Key Lab Metab Target Characterizat & Tradi, Dalian, Peoples R China
[2] Xuzhou Med Univ, Jiangsu Key Lab New Drug Res & Clin Pharm, Xuzhou, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Soluble epoxide hydrolase; Inhibition kinetics; Molecular dynamics simulations; DERIVATIVES; DISCOVERY; TARGET;
D O I
10.1016/j.ijbiomac.2021.04.187
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
Inhibition of soluble epoxide hydrolase (sEH) is considered to be an effective treatment for inflammation-related diseases, and small molecules origin from natural products show promising activity against sEH. Two undescribed protostanes, 3 beta-hydroxy-25-anhydro-alisol F (1) and 3 beta-hydroxy-alisol G (2) were isolated from Alisma orientate and identified as new sEH inhibitors with IC50 values of 10.06 and 30.45 mu M, respectively. Potential lead compound 1 was determined as an uncompetitive inhibitor against sEH, which had a Kj value of 5.13 mu M. In-depth molecular docking and molecular dynamics simulations revealed that amino acid residue Ser374 plays an important role in the inhibition of 1, which also provides an idea for the development of sEH inhibitors based on protostane-type triterpenoids. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:811 / 817
页数:7
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