2-Substituted piperazine-derived imidazole carboxamides as potent and selective CCK1R agonists for the treatment of obesity.
Berger, Richard
2-Substituted piperazine-derived imidazole carboxamides as potent and selective CCK1R agonists for the treatment of obesity. [electronic resource] - Bioorganic & medicinal chemistry letters Sep 2008 - 4833-7 p. digital
Publication Type: Comparative Study; Journal Article
1464-3405
10.1016/j.bmcl.2008.07.083 doi
Animals
Anti-Obesity Agents--chemical synthesis
Benzodiazepines--chemical synthesis
Chemokines, CC
Humans
Indoles--chemical synthesis
Methylamines--chemical synthesis
Mice
Obesity--drug therapy
Piperazine
Piperazines--chemistry
Receptor, Cholecystokinin A--agonists
Receptors, Cholecystokinin--agonists
Thiazoles--chemical synthesis
2-Substituted piperazine-derived imidazole carboxamides as potent and selective CCK1R agonists for the treatment of obesity. [electronic resource] - Bioorganic & medicinal chemistry letters Sep 2008 - 4833-7 p. digital
Publication Type: Comparative Study; Journal Article
1464-3405
10.1016/j.bmcl.2008.07.083 doi
Animals
Anti-Obesity Agents--chemical synthesis
Benzodiazepines--chemical synthesis
Chemokines, CC
Humans
Indoles--chemical synthesis
Methylamines--chemical synthesis
Mice
Obesity--drug therapy
Piperazine
Piperazines--chemistry
Receptor, Cholecystokinin A--agonists
Receptors, Cholecystokinin--agonists
Thiazoles--chemical synthesis