The Wayback Machine - https://web.archive.org/web/20120605121725/http://en.wikipedia.org/wiki/Vesamicol

Vesamicol

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Vesamicol
Systematic (IUPAC) name
2-(4-phenyl-1-piperidyl)cyclohexan-1-ol
Clinical data
Pregnancy cat.  ?
Legal status  ?
Identifiers
CAS number 22232-64-0
ATC code  ?
PubChem CID 5662
ChemSpider 5460
ChEMBL CHEMBL20730
Chemical data
Formula C17H25NO
Mol. mass 259.39 g/mol
SMILES eMolecules & PubChem

Vesamicol is an experimental drug, acting presynaptically by inhibiting acetylcholine (ACh) uptake and reducing its release.[1]

[edit] Mechanism of action

Vesamicol can be broadly categorized as a cholinergic physiological antagonist, because it reduces the apparent activity of cholinergic neurons, but does not act at the post-synaptic ACh receptor. Vesamicol causes a non-competitive and reversible block of the intracellular transporter responsible for carrying newly synthesised ACh into storage vesicles in the pre-synaptic nerve terminal. This transport process is driven by a proton gradient between cell organelles and the cytoplasm. Blocking of acetylcholine loading leads to empty vesicles fusing with neuron membranes, decreasing Ach release.

[edit] References

  1. ^ Salin-Pascual RJ, Jimenez-Anguiano A (October 1995). "Vesamicol, an acetylcholine uptake blocker in presynaptic vesicles, suppresses rapid eye movement (REM) sleep in the rat". Psychopharmacology 121 (4): 485–7. DOI:10.1007/BF02246498. PMID 8619013. 
Personal tools
Namespaces

Variants
Actions
Navigation
Interaction
Toolbox
Print/export
Morty Proxy This is a proxified and sanitized view of the page, visit original site.