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PMID: 18052088 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

On the intractability of estrogen-related receptor alpha as a target for activation by small molecules.

Journal of medicinal chemistry ·Vol. 50 ·No. 26 ·2007-12-27 ·Pages 6722-4

Hyatt SM, Lockamy EL, Stein RA, McDonnell DP, Miller AB, Orband-Miller LA, Willson TM, Zuercher WJ

Abstract

The estrogen-related receptor alpha (ERRalpha) is a potential target for activation in the treatment of metabolic disease. To date, no small-molecule agonists of ERRalpha have been identified despite several high-throughput screening campaigns. We describe the synthesis and profiling of a small array of compounds designed on the basis of a previously reported agonist-bound crystal structure of the closely related receptor ERRgamma. The results suggest that ERRalpha may be intractable as a direct target for pharmacologic activation.

MeSH Terms
Binding Sites Crystallography, X-Ray Drug Inverse Agonism Fluorescence Resonance Energy Transfer HeLa Cells Humans Hydrazones/chemical synthesis,chemistry,pharmacology Receptors, Estrogen/agonists,antagonists & inhibitors,chemistry
Chemicals
ERRalpha estrogen-related receptor Hydrazones Receptors, Estrogen
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Hyatt Stephen M
Molecular Discovery Research Branch, GlaxoSmithKline, Research Triangle Park, NC 27709, USA.
Lockamy Elizabeth L
Stein Rebecca A
McDonnell Donald P
Miller Aaron B
Orband-Miller Lisa A
Willson Timothy M
Zuercher William J
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Article Info
Journal
Journal of medicinal chemistry
Abbr.
J Med Chem
ISSN
0022-2623
Published
2007-12-27
Epub
2007-00-04
Pages
6722-4
Language
English
Region
United States
NLM ID
9716531
PMCID
PMC2556064
Subset
IM
Grants
NIDDK NIH HHS · R01 DK074652 · United States
NIDDK NIH HHS · R01 DK074652-01A2 · United States
NIDDK NIH HHS · DK074652 · United States
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