The imidazopyridines are a class of drugs defined by their chemical structure. In general, they are GABAA receptor agonists, however recently proton pump inhibitors, aromatase inhibitors, NSAIDs and other classes of drugs in this class have been developed as well. Despite usually being similar to them in effect, they are not chemically related to benzodiazepines. As such, GABAA-agonizing imidazopyridines, pyrazolopyrimidines, and cyclopyrrones are sometimes grouped together and referred to as "nonbenzodiazepines." Imidazopyridines include:
Anxiolytics, sedatives and hypnotics (GABAA receptor positive allosteric modulators):
- Alpidem (original brand name Ananxyl)—anxiolytic that was withdrawn from the market worldwide in 1995 due to hepatotoxicity.
- DS-1—a GABAA receptor positive allosteric modulator selective for the α4β3δ subtype, which is not targeted by other GABAergics such as benzodiazepines or other nonbenzodiazepines.
- Necopidem—an anxiolytic. It has not found clinical use.
- Saripidem—a sedative and anxiolytic. It is not used clinically.
- TP-003—a subtype-selective partial agonist at GABAA receptors, binding to GABAA receptor complexes bearing either α2, α3 or α5 subunits, but only showing significant efficacy at α3.
- Zolpidem (original brand name Ambien)—a widely used hypnotic. Generic versions are widely available.
- Mosapramine (brand name クレミン, Cremin)—an atypical antipsychotic used in Japan.
- CJ-033466—an experimental gastroprokinetic acting as a selective 5-HT4 serotonin receptor partial agonist.
- Zolimidine—a gastroprotective agent.
- Linaprazan—a potassium-competitive acid blocker which demonstrated similar efficacy as esomeprazole in healing and controlling symptoms of GERD patients with erosive esophagitis.
- SCH28080—the prototypical potassium-competitive acid blocker which has not found clinical use because of liver toxicity in animal trials and elevated liver enzyme activity in the serum of human volunteers.
- Telcagepant—a calcitonin gene-related peptide receptor antagonist which was in clinical trials as a remedy for migraine. Its development was terminated.
Drugs acting on the cardiovascular system:
Drugs for treatment of bone diseases:
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