New butenolide derivatives from the marine sponge-derived fungus Aspergillus terreus

被引:51
|
作者
Sun, Yating [1 ,2 ]
Liu, Jingtang [1 ]
Li, Lei [1 ]
Gong, Chi [2 ]
Wang, Shuping [1 ]
Yang, Fan [1 ]
Hua, Huiming [2 ]
Lin, Houwen [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp,Res Ctr Marine Drugs, Dept Pharm,State Key Lab Oncogenes & Related Gene, Shanghai 200127, Peoples R China
[2] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang 110016, Liaoning, Peoples R China
关键词
Aspergillus terreus; Butenolide derivatives; alpha-Glucosidase inhibitors; Antioxidant activity; ALPHA-GLUCOSIDASE INHIBITORS; ENDOPHYTIC FUNGUS; BUTYROLACTONES; ASPERNOLIDES;
D O I
10.1016/j.bmcl.2017.12.049
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Two new butenolide derivatives (+/-)-asperteretal D ((+/-)-1) and asperteretal E (2) containing rare 2-benzyl-3-phenyl substituted lactone core, together with nine known analogues (3-11) were obtained from a fungus Aspergillus terreus derived from the marine sponge Phakellia fusca. All the structures were elucidated on the basis of extensive NMR spectroscopic data. The chiral chromatography analyses allowed the separation of the (+/-)-asperteretal D, of which the absolute configurations were determined by comparing the experimental to calculated electronic circular dichroic (ECD) spectra. Compounds (+/-)-1, 2-5, and 7 exhibited potent inhibitory activities against alpha-glucosidase with IC50 values ranging from 8.65 to 20.3 mu M (positive control acarbose with an IC50 value of 320 mu M). In addition, derivatives 5-8 also showed moderate antioxidant activities. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:315 / 318
页数:4
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