Abstract
A series of potent amide linked PPARgamma/delta dual agonists (1a) has been discovered through rational design. In the ZDF rat model of type 2 diabetes, compound (R)-3-[4-(3-{1-[(5-chloro-1,3-dimethyl-1H-indole-2-carbonyl)-amino]-ethyl}-5-fluoro-phenoxy)-2-ethyl-phenyl]-propionic acid (42) from this series has demonstrated glucose lowering efficacy comparable to the marketed PPARgamma agonist rosiglitazone with less weight gain.
MeSH terms
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Amides / chemistry*
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Animals
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Combinatorial Chemistry Techniques
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Diabetes Mellitus, Type 2 / drug therapy
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Disease Models, Animal
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Drug Design*
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Indoles / chemical synthesis*
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Indoles / chemistry
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Indoles / pharmacology
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Molecular Structure
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PPAR delta / agonists*
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PPAR gamma / agonists*
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Rats
Substances
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(R)-3-(4-(3-(1-((5-chloro-1,3-dimethyl-1H-indole-2-carbonyl)amino)ethyl)-5-fluoro-phenoxy)-2-ethylphenyl)propionic acid
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Amides
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Indoles
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PPAR delta
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PPAR gamma