Original articleDesign, synthesis and biological evaluation of a novel class of potent TGR5 agonists based on a 4-phenyl pyridine scaffold
-
Add time:09/06/2019 Source:sciencedirect.com
TGR5, a GPCR, is involved in energy and glucose homeostasis, and as such, is a target for the treatment of diabetes, obesity and other metabolic syndromes. A new class of TGR5 agonists based on a 4-phenyl pyridine scaffold was designed, synthesized and evaluated in vitro and in vivo. Extensive structure–activity relationship studies are reported herein. The most potent compounds 15a, 18b and 18c showed comparable activity with the lead compound 2. 15a had the best potency in vitro but displayed an unfavorable pharmacokinetic profile and was found to be ineffective during an oral glucose tolerance test in imprinting control region mice at a dose of 50 mg/kg.
We also recommend Trading Suppliers and Manufacturers of 2-amino-1-(2-(trifluoromethyl)phenyl)ethanone hydrochloride (cas 111595-55-2). Pls Click Website Link as below: cas 111595-55-2 suppliers
Prev:Original articleTrifluoromethyl-promoted homocamptothecins: Synthesis and biological activity
Next:Evaluation of antidepressant activity of 1-(7-methoxy-2-methyl-1,2,3,4-tetrahydro-isoquinolin-4-YL)-cyclohexanol, a β-substituted phenylethylamine in mice) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Original articleTrifluoromethyl-promoted homocamptothecins: Synthesis and biological activity09/05/2019
- Original articleSynthesis of novel 1,2-benzothiazine 1,1-dioxide-3-ethanone oxime N-aryl acetamide ether derivatives as potent anti-inflammatory agents and inhibitors of monocyte-to-macrophage transformation09/04/2019
- Synthesis of novel trifluoromethyl-substituted spiro-[chromeno[4,3-d]pyrimidine-5,1′-cycloalkanes], and evaluation of their analgesic effects in a mouse pain model09/03/2019
- Synthesis and antinociceptive activity of new 2-substituted 4-(trifluoromethyl)-5,6-dihydrobenzo[h]quinazolines09/02/2019
-
Health and Chemical more >
-
Related Products


