化学
肠促胰岛素
小分子
药理学
糖尿病
生物化学
内分泌学
2型糖尿病
医学
作者
Santosh Kumar,Rakesh Ishwar Patil,Sazid Ali,Rakesh Kumar,Mohd Imran Khan,Amit Panwar,Srinivasa Reddy Mallampati,Muneeb Ahsan,Sunil S. Iyer,Arun Kumar
标识
DOI:10.1021/acs.jmedchem.5c00540
摘要
GPR119 modulation is reported to have a promising role for preventing or managing various metabolic disorders, including type 2 diabetes, insulin resistance, loss of beta cell function, hyperlipidemia, obesity, fatty liver, MASH, and cirrhosis. We have developed a potent GPR119 agonist, MKP10241, which has elevated cyclic adenosine monophosphate (cAMP) levels in the GPR119 expressing cell line and reduced blood glucose levels and HbA1c in acute models and a chronic diabetic mouse model. Chronic treatment of MKP10241 in DIO-mice exhibited marked reduction in body weight and feed intake at tested doses, which was associated with decreased blood glucose level, lipid parameters, and body fats. Further evaluation of MKP10241 in the STAM mouse model of MASH/MASLD showed significant MASH resolution. MKP10241 was evaluated in preclinical toxicity and genotoxicity studies in rats and dogs and found safe. Considering the preclinical safety and efficacy profile, MKP10241 has been advanced for safety, tolerability, and pharmacokinetic evaluation in healthy volunteers in a Phase-I clinical trial.
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