Abstract
A novel series of 5-aryl thiazolidine-2,4-diones based dual PPARalpha/gamma agonists was identified. A number of highly potent and orally bioavailable analogues were synthesized. Efficacy study results of some of these analogues in the db/db mice model of type 2 diabetes showed them superior to rosiglitazone in correcting hyperglycemia and hypertriglyceridemia.
MeSH terms
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Administration, Oral
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Animals
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Diabetes Mellitus, Type 2 / drug therapy
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Disease Models, Animal
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Hyperglycemia / drug therapy
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Hypertriglyceridemia / drug therapy
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Hypoglycemic Agents / chemical synthesis*
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Hypoglycemic Agents / pharmacology
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Mice
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Receptors, Cytoplasmic and Nuclear / agonists*
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Receptors, Cytoplasmic and Nuclear / metabolism
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Rosiglitazone
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Structure-Activity Relationship
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Thiazolidinediones / chemical synthesis*
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Thiazolidinediones / pharmacology
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Transcription Factors / agonists*
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Transcription Factors / metabolism
Substances
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Hypoglycemic Agents
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Receptors, Cytoplasmic and Nuclear
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Thiazolidinediones
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Transcription Factors
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Rosiglitazone