Abstract
A new class of MCHR1 antagonists was discovered via a high-throughput screen. Optimization of the lead structure resulted in the identification of indole 10e. This compound possesses good pharmacokinetic properties across preclinical species and is efficacious in reducing food consumption in an MCH cannulated rat model and a cynomolgus monkey food consumption model.
Copyright © 2011 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Anti-Obesity Agents / chemical synthesis
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Anti-Obesity Agents / chemistry*
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Anti-Obesity Agents / pharmacokinetics
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Anti-Obesity Agents / pharmacology
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Dogs
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Drug Discovery*
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Eating / drug effects
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HEK293 Cells
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Humans
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Indoles / chemical synthesis
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Indoles / chemistry*
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Indoles / pharmacology
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Inhibitory Concentration 50
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Macaca mulatta
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Molecular Structure
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Rats
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Receptors, Pituitary Hormone / antagonists & inhibitors*
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Structure-Activity Relationship
Substances
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Anti-Obesity Agents
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Indoles
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Receptors, Pituitary Hormone
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melanin-concentrating hormone receptor
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indole