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Bioorg Med Chem Lett ; 22(18): 5857-62, 2012 Sep 15.
Article in English | MEDLINE | ID: mdl-22917520

ABSTRACT

Series of benzyl-phenoxybenzyl amino-phenyl acid derivatives (8a-q) are reported as non-steroidal GR antagonist. Compound 8g showed excellent h-GR binding and potent antagonistic activity (in vitro). The lead compound 8g exhibited significant oral antidiabetic and antihyperlipidemic effects (in vivo), along with liver selectivity. These preliminary results confirm discovery of potent and liver selective passive GR antagonist for the treatment of T2DM.


Subject(s)
Benzyl Compounds/pharmacology , Diabetes Mellitus, Type 2/drug therapy , Drug Discovery , Hypoglycemic Agents/pharmacology , Liver/chemistry , Receptors, Glucocorticoid/antagonists & inhibitors , Administration, Oral , Animals , Benzyl Compounds/administration & dosage , Benzyl Compounds/chemistry , Blood Glucose/drug effects , Dose-Response Relationship, Drug , Focal Adhesion Protein-Tyrosine Kinases/antagonists & inhibitors , Gene Products, tat/antagonists & inhibitors , Humans , Hypoglycemic Agents/administration & dosage , Hypoglycemic Agents/chemistry , Liver/drug effects , Liver/metabolism , Male , Mice , Mice, Obese , Models, Molecular , Molecular Structure , Rats , Rats, Sprague-Dawley , Structure-Activity Relationship
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