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PMID: 16983687 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Review

Acetyl-coenzyme A carboxylases: versatile targets for drug discovery.

Journal of cellular biochemistry ·Vol. 99 ·No. 6 ·2006-12-15 ·Pages 1476-88

Tong L, Harwood HJ

Abstract

Acetyl-coenzyme A carboxylases (ACCs) have crucial roles in fatty acid metabolism in humans and most other living organisms. They are attractive targets for drug discovery against a variety of human diseases, including diabetes, obesity, cancer, and microbial infections. In addition, ACCs from grasses are the targets of herbicides that have been in commercial use for more than 20 years. Significant progresses in both basic research and in drug discovery have been made over the past few years in the studies on these enzymes. At the basic research level, the crystal structures of the biotin carboxylase (BC) and the carboxyltransferase (CT) components of ACC have been determined, and the molecular basis for ACC inhibition by small molecules are beginning to be understood. At the drug discovery level, a large number of nanomolar inhibitors of mammalian ACCs have been reported and the extent of their therapeutic potential is being aggressively explored. This review summarizes these new progresses and also offers some prospects in terms of the future directions for the studies on these important enzymes.

MeSH Terms
Acetyl-CoA Carboxylase/antagonists & inhibitors,chemistry Animals Drug Design Enzyme Inhibitors/chemistry,pharmacology Humans Models, Molecular Protein Conformation
Chemicals
Enzyme Inhibitors Acetyl-CoA Carboxylase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tong Liang
Department of Biological Sciences, Columbia University, New York, NY 10027, USA. [email protected]
Harwood H James
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Article Info
Journal
Journal of cellular biochemistry
Abbr.
J Cell Biochem
ISSN
0730-2312
Published
2006-12-15
Pages
1476-88
Language
English
Region
United States
NLM ID
8205768
PMCID
PMC3837461
Subset
IM
Grants
NIDDK NIH HHS · R01 DK067238 · United States
NIDDK NIH HHS · R01 DK067238-05A2 · United States
NIDDK NIH HHS · DK 67238 · United States
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