Heteroaryl substituted bis-trifluoromethyl carbinols as malonyl-CoA decarboxylase inhibitors

被引:18
作者
Cheng, Jie-Fei
Mak, Chi Ching
Huang, Yujin
Penuliar, Richard
Nishimoto, Masahiro
Zhang, Lin
Chen, Mi
Wallace, David
Arrhenius, Thomas
Chu, Donald
Yang, Guang
Barbosa, Miguel
Barr, Rick
Dyck, Jason R. B.
Lopaschuk, Gary D.
Nadzan, Alex M.
机构
[1] Chugai Pharma LLC, Dept Chem & Discovery Biol, San Diego, CA 92121 USA
[2] Univ Alberta, Metab Modulator Res Ltd, Res Transit Facil 2020, Edmonton, AB, Canada
关键词
malonyl-CoA; acetyl-CoA; malonyl-CoA decarboxylase; MCD; fatty acid oxidation; glucose oxidation;
D O I
10.1016/j.bmcl.2006.03.100
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of heteroaryl-substituted bis-trifluoromethyl carbinols were prepared and evaluated as malonyl-CoA decarboxylase (MCD) inhibitors. Some thiazole-based derivatives showed potent in vitro MCD inhibitory activities and significantly increased glucose oxidation rates in isolated working rat hearts. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3484 / 3488
页数:5
相关论文
共 52 条
[1]   Malonyl-CoA and the regulation of fatty acid oxidation in soleus muscle [J].
Alam, N ;
Saggerson, ED .
BIOCHEMICAL JOURNAL, 1998, 334 :233-241
[2]  
BARR R, 1997, MEASUREMENT CARDIOVA, P19
[3]   New reactions in the crotonase superfamily:: Structure of methylmalonyl CoA decarboxylase from Escherichia coli [J].
Benning, MM ;
Haller, T ;
Gerlt, JA ;
Holden, HM .
BIOCHEMISTRY, 2000, 39 (16) :4630-4639
[4]   2-(N,N-DISUBSTITUTED AMINO)THIAZOLES WITH ELECTRON-WITHDRAWING GROUPS AT POSITION 5 - PREPARATION AND INVESTIGATION OF STRUCTURAL FEATURES [J].
BIRKINSHAW, TN ;
GILLON, DW ;
HARKIN, SA ;
MEAKINS, GD ;
TIREL, MD .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1984, (02) :147-153
[5]   Synthesis and structure-activity relationship of small-molecule malonyl coenzyme A decarboxylase inhibitors [J].
Cheng, JF ;
Chen, M ;
Wallace, D ;
Tith, S ;
Haramura, M ;
Liu, B ;
Mak, CC ;
Arrhenius, T ;
Reily, S ;
Brown, S ;
Thorn, V ;
Harmon, C ;
Barr, R ;
Dyck, JRB ;
Lopaschuk, GD ;
Nadzan, AM .
JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (05) :1517-1525
[6]   Design and synthesis of heterocyclic malonyl-CoA decarboxylase inhibitors [J].
Cheng, JF ;
Chen, M ;
Liu, B ;
Hou, Z ;
Arrhenius, T ;
Nadzan, AM .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (03) :695-700
[7]   Malonyl-CoA content and fatty acid oxidation in rat muscle and liver in vivo [J].
Chien, D ;
Dean, D ;
Saha, AK ;
Flatt, JP ;
Ruderman, NB .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 279 (02) :E259-E265
[8]  
DYCK JR, 1998, AM J PHYSIOL, V27, pH2122
[9]   Malonyl coenzyme a decarboxylase inhibition protects the ischemic heart by inhibiting fatty acid oxidation and stimulating glucose oxidation [J].
Dyck, JRB ;
Cheng, JF ;
Stanley, WC ;
Barr, R ;
Chandler, MP ;
Brown, S ;
Wallace, D ;
Arrhenius, T ;
Harmon, C ;
Yang, G ;
Nadzan, AM ;
Lopaschuk, GD .
CIRCULATION RESEARCH, 2004, 94 (09) :E78-E84
[10]   The molecular basis of malonyl-CoA decarboxylase deficiency [J].
FitzPatrick, DR ;
Hill, A ;
Tolmie, JL ;
Thorburn, DR ;
Christodoulou, L .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (02) :318-326