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Ipidacrine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Ipidacrine
Clinical data
Trade namesNeiromidin
Other namesAmiridine; NIK-247
ATC code
Legal status
Legal status
Identifiers
  • 2,3,5,6,7,8-Hexahydro-1H-cyclopenta[b]quinolin-9-amine
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.201.385Edit this at Wikidata
Chemical and physical data
FormulaC12H16N2
Molar mass188.274 g·mol−1
3D model (JSmol)
  • C1CCc2c(c(c3c(n2)CCC3)N)C1
  • InChI=1S/C12H16N2/c13-12-8-4-1-2-6-10(8)14-11-7-3-5-9(11)12/h1-7H2,(H2,13,14)
  • Key:YLUSMKAJIQOXPV-UHFFFAOYSA-N

Ipidacrine (Neiromidin) is a drug first synthesized by the National Research Center for Biologically Active Compounds in theRussian Federation. This compound is a modification of the older drugtacrine (Cognex).[1]

Ipidacrine is a reversibleacetylcholinesterase inhibitor used in memory disorders of different origins.[2][3][4]

Ipidacrine directly stimulates impulse transmission in thecentral nervous system and neuromuscular synapses by blocking membranepotassium channels. Ipidacrine enhances not onlycholine, but alsoadrenaline,serotonin,histamine, andoxytocin effects on smooth muscle.[5]

See also

[edit]

References

[edit]
  1. ^Kojima J, Onodera K, Ozeki M, Nakayarna K (1998)."Ipidacrine (NIK-247): A Review of Multiple Mechanisms as an Antidementia Agent".CNS Drug Reviews.4 (3):247–259.doi:10.1111/j.1527-3458.1998.tb00067.x.
  2. ^Damulin IV, Stepkina DA, Lokshina AB (2011). "[Neuromidin in mixed vascular and Alzheimer's dementia]".Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova.111 (2):40–3.PMID 21350422.
  3. ^Pustokhanova LV, Morozova EM (2011). "[Cognitive disorders in the early rehabilitation period of ischemic stroke and possibilities of their treatment with neuromidin]".Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova.111 (4 Pt 2):23–7.PMID 23120773.
  4. ^Onodera K, Kojima J, Wachi M (April 1998). "Ipidacrine (NIK-247), a novel antidementia, rapidly enters the brain and improves scopolamine-induced amnesia in rats during the Morris water maze task".Nihon Shinkei Seishin Yakurigaku Zasshi = Japanese Journal of Psychopharmacology.18 (2):33–7.PMID 9656230.
  5. ^"Neiromidin Product Information". Archived fromthe original on 2013-06-13. Retrieved2013-05-30.
Psychoanaleptics: Anti-dementia agents (ATC codeN06D and others)
AChE inhibitor medications
Other medications
ExperimentalBACE inhibitors
Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
Enhancers
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