Chemistry:Ropanicant

From HandWiki

Ropanicant (SUVN-911) is an investigational new drug under development by Suven Life Sciences Ltd for the treatment of major depressive disorder (MDD) and other neurological conditions. It acts as an antagonist of the α4β2 nicotinic acetylcholine receptor (nAChR), a target involved in mood regulation and cognitive function. Ropanicant has been shown to increase levels of serotonin and brain-derived neurotrophic factor (BDNF) in the cortex, which may contribute to its antidepressant effects.[1] By modulating neurotransmitter levels—particularly serotonin—it is intended to produce rapid antidepressant effects while minimizing the side effects commonly associated with traditional antidepressants.

Clinical trials

The compound has completed Phase 1 and Phase 2 clinical trials for moderate to severe major depressive disorder.[2][1] Preliminary studies have explored its potential for a faster onset of action compared to conventional antidepressants.[3] In addition to its investigation in depression, ongoing research is examining its possible use in treating neurodegenerative disorders such as Alzheimer’s disease.[4]

See also

References

  1. 1.0 1.1 "Ropanicant (SUVN-911), an α4β2 nicotinic acetylcholine receptor antagonist intended for the treatment of depressive disorders: pharmacological, behavioral, and neurochemical characterization". Psychopharmacology 239 (7): 2215–2232. July 2022. doi:10.1007/s00213-022-06108-6. PMID 35298691. 
  2. "Safety, Tolerability, and Pharmacokinetics of Ropanicant (SUVN-911), a Novel Alpha4 Beta2 Nicotinic Acetylcholine Receptor (α4β2 nAChR) Antagonist, in Healthy Adult and Elderly Subjects". Clinical Drug Investigation 42 (9): 747–762. September 2022. doi:10.1007/s40261-022-01189-9. PMID 35963959. 
  3. "Discovery and Development of 3-(6-Chloropyridine-3-yloxymethyl)-2-azabicyclo[3.1.0]hexane Hydrochloride (SUVN-911): A Novel, Potent, Selective, and Orally Active Neuronal Nicotinic Acetylcholine α4β2 Receptor Antagonist for the Treatment of Depression". Journal of Medicinal Chemistry 63 (6): 2833–2853. March 2020. doi:10.1021/acs.jmedchem.9b00790. PMID 32026697. 
  4. "Synthesis of SUVN-911.". Synfacts 16 (626): 0626. June 2020. doi:10.1055/s-0040-1707534.