Hydroxycoumarin Derivatives: Novel and Potent α-Glucosidase Inhibitors

被引:90
作者
Shen, Qiong [1 ,2 ,3 ]
Shao, Jialiang [2 ]
Peng, Quan [2 ]
Zhang, Wanjin [3 ]
Ma, Lin [2 ]
Chan, Albert S. C. [3 ]
Gu, Lianquan [3 ]
机构
[1] Univ Nottingham, Sch Pharm, Nottingham NG7 2RD, England
[2] Sun Yat Sen Univ, Sch Chem & Chem Engn, Guangzhou 510275, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510275, Guangdong, Peoples R China
关键词
BUTYLDEOXYNOJIRIMYCIN-MEDIATED INHIBITION; ACETYLCHOLINESTERASE INHIBITORS; CHEMOPREVENTIVE AGENTS; BETA-GALACTOSIDASE; GERMINATING-SEEDS; VIGNA-SINENSIS; COUMARINS; ACID; 4-HYDROXYCOUMARINS; GLYCOSYLATION;
D O I
10.1021/jm100757r
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A novel class of hydroxycoumarin derivatives were found to be potent alpha-glucosidase inhibitors. Their syntheses were reported and the structure-activity relationship was established. Kinetic enzymatic assays indicated that compound 10 was a slow-binding and noncompetitive inhibitor with a K-i value of 589 nM, while compound 11 was a competitive inhibitor with a K-i value of 4.810 mu M. Among all hydroxycoumarin derivatives studied, compounds 10 and 11 exhibited the highest activities, were specific inhibitors of alpha-glucosidase, and could be exploited as the lead compounds for the development of potent alpha-glucosidase inhibitors. Compounds 10 and 11 were also selected for further discussion for the mechanism of enzymatic inhibition.
引用
收藏
页码:8252 / 8259
页数:8
相关论文
共 41 条
[1]  
Bernfeld P., 1955, Methods in enzymology, V1
[2]   BETA-GALACTOSIDASE ACTIVITY IN THE GERMINATING-SEEDS OF VIGNA-SINENSIS [J].
BISWAS, TK .
PHYTOCHEMISTRY, 1985, 24 (12) :2831-2833
[3]   CATIONIC FORM OF BETA-GALACTOSIDASE IN THE GERMINATING-SEEDS OF VIGNA-SINENSIS (LINN) SAVI [J].
BISWAS, TK .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 251 (01) :379-384
[4]   MECHANISM-BASED INHIBITION OF YEAST ALPHA-GLUCOSIDASE AND HUMAN PANCREATIC ALPHA-AMYLASE BY A NEW CLASS OF INHIBITORS - 2-DEOXY-2,2-DIFLUORO-ALPHA-GLYCOSIDES [J].
BRAUN, C ;
BRAYER, GD ;
WITHERS, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (45) :26778-26781
[5]   Kinetics of inhibition of β-glucosidase from Ampullarium crossean by bromoacetic acid [J].
Chen, QX ;
Zhang, Z ;
Zhou, XW ;
Zhuang, ZL .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (07) :717-723
[6]   Trapped in the act of catalysis [J].
Davies, GJ ;
Wilson, KS .
NATURE STRUCTURAL BIOLOGY, 1999, 6 (05) :406-408
[7]   Seeking sweet relief for diabetes [J].
Dove, A .
NATURE BIOTECHNOLOGY, 2002, 20 (10) :977-981
[8]   An efficient large scale synthesis of coumarins by a dealkylative boron-mediated ring closure of 3-(orthomethoxyaryl)propenoic esters. [J].
Dubuffet, T ;
Loutz, A ;
Lavielle, G .
SYNTHETIC COMMUNICATIONS, 1999, 29 (06) :929-936
[9]   Targeting glycosylation as a therapeutic approach [J].
Dwek, RA ;
Butters, TD ;
Platt, FM ;
Zitzmann, N .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (01) :65-75
[10]   N-butyldeoxynojirimycin-mediated inhibition of human immunodeficiency virus entry correlates with changes in antibody recognition of the V1/V2 region of gp120 [J].
Fischer, PB ;
Karlsson, GB ;
Butters, TD ;
Dwek, RA ;
Platt, FM .
JOURNAL OF VIROLOGY, 1996, 70 (10) :7143-7152