Design, synthesis and evaluation of novel azasugar-based MMP/ADAM inhibitors

被引:14
作者
Moriyama, H
Tsukida, T
Inoue, Y
Kondo, H
Yoshino, K
Nishimura, SI
机构
[1] Japan Bioind Assoc, Hokkaido Collaborat Ctr, Sapporo, Hokkaido 0010021, Japan
[2] Nippon Organon KK, R&D Labs, Miyakojima Ku, Osaka 5340016, Japan
[3] Hokkaido Univ, Grad Sch Sci, Div Biol Sci, Kita Ku, Sapporo, Hokkaido 0010021, Japan
关键词
D O I
10.1016/S0960-894X(03)00531-6
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In order to verify whether azasugar would be a useful scaffold for inhibitory activity against metalloproteinases, we synthesized some azasugar-based compounds. As a result, it is clarified that azasugar moiety could function as successful inhibitor of matrix metalloproteinase-1, -3 and -9 and TACE. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2741 / 2744
页数:4
相关论文
共 21 条
[1]   Recent advances in matrix metalloproteinase inhibitor research [J].
Beckett, RP ;
Davidson, AH ;
Drummond, AH ;
Huxley, P ;
Whittaker, M .
DRUG DISCOVERY TODAY, 1996, 1 (01) :16-26
[2]   Matrix metalloproteinase inhibitors 1998 [J].
Beckett, RP ;
Whittaker, M .
EXPERT OPINION ON THERAPEUTIC PATENTS, 1998, 8 (03) :259-282
[3]  
Bemelmans MHA, 1996, CRIT REV IMMUNOL, V16, P1
[4]   ADAMs: focus on the protease domain [J].
Black, RA ;
White, JM .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (05) :654-659
[5]   Matrix metalloproteinase expression during experimental autoimmune encephalomyelitis and effects of a combined matrix metalloproteinase and tumour necrosis factor-alpha inhibitor [J].
Clements, JM ;
Cossins, JA ;
Wells, GMA ;
Corkill, DJ ;
Helfrich, K ;
Wood, LM ;
Pigott, R ;
Stabler, G ;
Ward, GA ;
Gearing, AJH ;
Miller, KM .
JOURNAL OF NEUROIMMUNOLOGY, 1997, 74 (1-2) :85-94
[6]  
Grandel R, 1996, LIEBIGS ANN, P1143
[7]   A short synthesis of azasugars via aldol reaction of chelated amino acid ester enolates [J].
Grandel, R ;
Kazmaier, U .
TETRAHEDRON LETTERS, 1997, 38 (46) :8009-8012
[8]   DEOXYNOJIRIMYCIN - SYNTHESIS AND BIOLOGICAL-ACTIVITY [J].
HUGHES, AB ;
RUDGE, AJ .
NATURAL PRODUCT REPORTS, 1994, 11 (02) :135-162
[9]  
Michaelides MR, 1999, CURR PHARM DESIGN, V5, P787
[10]   THE USE OF DIETHYL AZODICARBOXYLATE AND TRIPHENYLPHOSPHINE IN SYNTHESIS AND TRANSFORMATION OF NATURAL-PRODUCTS [J].
MITSUNOBU, O .
SYNTHESIS-STUTTGART, 1981, (01) :1-28