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gabapentin

File:GabapentinStructure.svg · Wikimedia Commons · See Wikimedia Commons

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gabapentin

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Also known as CI 945, Go 3450, GOE 2450, GOE 3450, Neurontin®, 1-(Aminomethyl)cyclohexaneacetic acid, Gabapetin, Aclonium

Gabapentin, sold under the brand name Neurontin among others, is an anticonvulsant medication used to treat neuropathic pain (postherpetic neuralgia) and partial seizures of epilepsy. Gabapentin is a central nervous system (CNS) depressant and derivative of the inhibitory neurotransmitter, GABA. It is used for the treatment of neuropathic pain caused by diabetic neuropathy, postherpetic neuralgia, and central pain. It is moderately effective: about 30–40% of those given gabapentin for diabetic neuropathy or postherpetic neuralgia have a meaningful benefit.

OverviewAI-generated

Gabapentin is a chemical compound with the formula C₉H₁₇NO₂. Its IUPAC name is 2-[1-(azaniumylmethyl)cyclohexyl]acetate. The substance has a mass of 171.126 and a weight of 171.24. It possesses a defined daily dose of 1.8.

Chemical properties include an xlogp of -0.5 and a topological polar surface area of 67.8. The molecule contains one hydrogen bond donor and two hydrogen bond acceptors, with a charge of 0.

The compound is referenced by 1,354 other encyclopedia articles. A search for gabapentin in PubMed yields a count of 9602.

Synthesized by Vinony from 18 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.

Key facts

Drug.onset
2-3 hours
Drug.image
GabapentinStructure.svg
Drug.image_class
skin-invert-image
Drug.tradename
Neurontin, others
Drug.MedlinePlus
a694007
Drug.DailyMedID
Gabapentin
Drug.pregnancy_AU
B1
Drug.dependency_liability
Physical: HighPsychological: Moderate
Drug.addiction_liability
Low
Drug.routes_of_administration
By mouth
Drug.ATC_prefix
N02
Drug.ATC_suffix
BF01
Drug.legal_AU
S4
Drug.legal_BR
C1
Drug.legal_CA
Rx-only
Drug.legal_UK
Class C
Drug.legal_US
Schedule V controlled substance (Select States)
Drug.bioavailability
27–60% (inversely proportional to dose; a high-fat meal also increases bioavailability)

via Wikipedia infobox

Chemical data

Formula
C9H17NO2
Molecular weight
171.24 g/mol
IUPAC name
2-[1-(azaniumylmethyl)cyclohexyl]acetate
SMILES
C1CCC(CC1)(CC(=O)[O-])C[NH3+]
InChIKey
UGJMXCAKCUNAIE-UHFFFAOYSA-N
XLogP
-0.5
Polar surface area
67.8 Ų
H-bond donors
1
H-bond acceptors
2
Formal charge
0

via PubChem

Research

9,602 papers

via PubMed

~31 min read

Encyclopedic overview

35 sections
Contents
  • Medical uses
  • Seizures
  • Neuropathic pain
  • Anxiety
  • Sleep
  • Drug dependence
  • Other
  • Contraindications
  • Side effects
  • Suicide
  • Respiratory depression
  • Withdrawal and dependence
  • Psychiatric and behavioral adverse effects
  • Overdose
  • Pharmacology
  • Animal models
  • Pharmacodynamics
  • Pharmacokinetics
  • Chemistry
  • Synthesis
  • History
  • Society and culture
  • Legal status
  • United Kingdom
  • United States
  • Off-label promotion
  • ''Franklin v. Parke-Davis'' case
  • Gabasync
  • Usage trends
  • Brand names
  • Related drugs
  • Recreational use
  • Veterinary use
  • References
  • External links

Gabapentin, sold under the brand name Neurontin among others, is an anticonvulsant medication used to treat neuropathic pain (postherpetic neuralgia) and partial seizures of epilepsy. Gabapentin is a central nervous system (CNS) depressant and derivative of the inhibitory neurotransmitter, GABA. It is used for the treatment of neuropathic pain caused by diabetic neuropathy, postherpetic neuralgia, and central pain. It is moderately effective: about 30–40% of those given gabapentin for diabetic neuropathy or postherpetic neuralgia have a meaningful benefit.

Gabapentin acts by decreasing activity of the α2δ-1 protein, coded by the CACNA2D1 gene, first known as an auxiliary subunit of voltage-gated calcium channels. By binding to α2δ-1, gabapentin reduces the release of excitatory neurotransmitters (primarily glutamate) and as a result, reduces excess excitation of neuronal networks in the spinal cord and brain. Sleepiness and dizziness are the most common side effects. Serious side effects include respiratory depression and allergic reactions. On December 16, 2008, the FDA issued gabapentin a class warning for an increased risk of suicide. Approximately two years after this pronouncement, a pharmacoepidemiologic study was conducted that showed there was no outstanding difference in suicide attempt rates between pre- and post- gabapentin prescription groups.

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

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