Skip to content
tiagabine

Structure via PubChem · Public domain (PubChem)

EntityQ907219· pop 20· linked from 617 articles

Also known as ABBOTT-70569, ABT-569, Gabitril®, tiagabine hydrochloride, Tiagabina, Tiagabinum

Tiagabine, sold under the brand name Gabitril, is an anticonvulsant medication which is used in the treatment of epilepsy. It is also used off-label in the treatment of insomnia and anxiety disorders. However, off-label use is discouraged as the drug has been associated with new-onset seizures in people without epilepsy. Tiagabine is taken orally.

Chemical data

Formula
C20H25NO2S2
Molecular weight
375.6 g/mol
IUPAC name
(3R)-1-[4,4-bis(3-methylthiophen-2-yl)but-3-enyl]piperidin-1-ium-3-carboxylate
SMILES
CC1=C(SC=C1)C(=CCC[NH+]2CCC[C@H](C2)C(=O)[O-])C3=C(C=CS3)C
InChIKey
PBJUNZJWGZTSKL-MRXNPFEDSA-N
XLogP
3.3
Polar surface area
101 Ų
H-bond donors
1
H-bond acceptors
4
Formal charge
0

via PubChem

Research

1,071 papers

via PubMed

~14 min read

Encyclopedic overview

27 sections
Contents
  • Medical uses
  • Epilepsy
  • Other uses
  • Insomnia
  • Anxiety disorders
  • Neuropathic pain
  • Available forms
  • Contraindications
  • Side effects
  • Overdose
  • Interactions
  • Pharmacology
  • Pharmacodynamics
  • Pharmacokinetics
  • Absorption
  • Distribution
  • Metabolism
  • Elimination
  • Chemistry
  • History
  • Society and culture
  • Availability
  • Legal status
  • Research
  • See also
  • References
  • External links

Tiagabine, sold under the brand name Gabitril, is an anticonvulsant medication which is used in the treatment of epilepsy. It is also used off-label in the treatment of insomnia and anxiety disorders. However, off-label use is discouraged as the drug has been associated with new-onset seizures in people without epilepsy. Tiagabine is taken orally.

Side effects of tiagabine include dizziness, asthenia, non-specific nervousness, muscle tremors, diarrhea, depression, and emotional lability. The drug acts as a selective GABA transporter 1 (GAT-1) blocker or GABA reuptake inhibitor, and hence acts as an indirect GABA receptor agonist, increasing GABAergic signaling in the brain. It may increase activation of both GABAA and GABAB receptors. The effects of tiagabine on sleep resemble those of GABAA receptor agonists like gaboxadol and muscimol, primarily enhancing slow wave sleep, and differ from those of GABAA receptor positive allosteric modulators like benzodiazepines and Z drugs. The drug's elimination half-life is 4.5 to 9hours, but can be shorter in people taking enzyme-inducing anticonvulsants.

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

Gallery (3)