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latrepirdine

Structure via PubChem · Public domain (PubChem)

EntityQ408580· pop 8· linked from 1,859 articles

latrepirdine

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Latrepirdine (INN, also known as dimebolin and sold as Dimebon) is an antihistamine drug which has been used clinically in Russia since 1983.

In the Vinony graph

Within Vinony's link graph, latrepirdine is referenced by 1,859 other articles, and connects out to propranolol, adrenergic receptor and N-methylserotonin.

Vinony files it under Chemical pages without DrugBank identifier, Drugs in the Soviet Union and Drugs not assigned an ATC code.

Its subject is documented across 7 Wikipedia language editions.

Chemical data

Formula
C21H25N3
Molecular weight
319.4 g/mol
IUPAC name
2,8-dimethyl-5-[2-(6-methyl-3-pyridinyl)ethyl]-3,4-dihydro-1H-pyrido[4,3-b]indole
SMILES
CC1=CC2=C(C=C1)N(C3=C2CN(CC3)C)CCC4=CN=C(C=C4)C
InChIKey
JNODQFNWMXFMEV-UHFFFAOYSA-N
XLogP
3.5
Polar surface area
21.1 Ų
H-bond donors
0
H-bond acceptors
2
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 3
Molecule type
Small molecule
Indications
Alzheimer disease, Huntington disease, liver failure

via ChEMBL · EBI

Wikidata facts

Has part
carbon
Mass
319.205
Show 4 more facts
chemical formula
C₂₁H₂₅N₃
canonical SMILES
CC1=CC2=C(C=C1)N(C3=C2CN(CC3)C)CCC4=CN=C(C=C4)C
Commons category
Latrepirdine
subject has role
nootropic
Sources (2)

via Wikidata · CC0

~4 min read

Encyclopedic overview

7 sections
Contents
  • Uses
  • Clinical trials
  • Alzheimer's disease
  • Huntington's disease
  • Pharmacology
  • See also
  • References

Latrepirdine (INN, also known as dimebolin and sold as Dimebon) is an antihistamine drug which has been used clinically in Russia since 1983.

Research was conducted in both Russia and western nations into potential applications as a neuroprotective drug to treat Alzheimer's disease and, possibly, as a nootropic, as well. After a major phase III clinical trial for Alzheimer's disease (AD) treatment failed to show any benefit, three other AD trials continued. Major industry-based development in this indication essentially stopped after another Phase III trial suffered the same fate in 2012. Latrepirdine failed in the phase III trial for Huntington's disease.

Excerpted from Wikipedia’s “latrepirdine” article, available under the CC BY-SA 4.0 licence.

Available in 7 languages

via Wikidata sitelinks · CC0

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