Mesh : Animals Diabetes Mellitus, Type 2 / drug therapy Diacylglycerol O-Acyltransferase / antagonists & inhibitors metabolism Dipeptidyl Peptidase 4 / metabolism Dose-Response Relationship, Drug Humans Hypoglycemic Agents / chemical synthesis chemistry pharmacology JNK Mitogen-Activated Protein Kinases / antagonists & inhibitors metabolism Molecular Structure Peroxisome Proliferator-Activated Receptors / metabolism Protein Tyrosine Phosphatases / antagonists & inhibitors metabolism Receptors, Adrenergic, beta-3 / metabolism Receptors, Histamine H3 / metabolism Structure-Activity Relationship Thiadiazoles / chemical synthesis chemistry pharmacology

来  源:   DOI:10.2174/1389557513666140103102447

Abstract:
This review provides a brief summary of thiadiazole ring containing compounds as antidiabetic agents. It covers the most active thiadiazole derivatives selected from reported literature of thiadiazole system as antidiabetic drug substance in the form of synthesis and structural activity relationship study reports. Some of the promising thiadiazole compounds interacting with targets such as sodium-glucose linked transporter, peroxisome proliferator-activated receptor, protein tyrosine phosphatase, c-Jun N-terminal kinase, dipeptidyl peptidase-4 and cannabinoid-1 receptor have been collected with their biological potency. The information provided in this review acts as important overview for medicinal chemist to develop a new chemical entity possessing antidiabetic activity.
摘要:
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