Tetrabenazine

CHEMBL117785 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
317.4 g/mol
LogP
2.9
Phase
4

Tetrabenazine is a monoamine-depleting agent that reversibly inhibits vesicular monoamine transporter 2 (VMAT2), blocking the packaging of dopamine, serotonin, and norepinephrine into synaptic vesicles and depleting presynaptic monoamine stores. It is approved for the treatment of chorea associated with Huntington's disease, and is also used for hemiballismus, tardive dyskinesia, and other hyperkinetic movement disorders. Central dopamine depletion reduces involuntary movements but can cause depression, sedation, and parkinsonism as adverse effects.

Molekularmasse

317,4000 g/mol

LogP

2,90

TPSA

38,80 Ų

Lipinski-Regel der Fünf

Bestanden

Therapeutische Bereiche

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D-Struktur

SVG PNG

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SMILES

COc1cc2c(cc1OC)C1CC(=O)C(CC(C)C)CN1CC2

InChI

InChI=1S/C19H27NO3/c1-12(2)7-14-11-20-6-5-13-8-18(22-3)19(23-4)9-15(13)16(20)10-17(14)21/h8-9,12,14,16H,5-7,10-11H2,1-4H3

Molecular Formula

C19H27NO3

HBD / HBA

- / 4

Rotierbare Bindungen

4

Schwere Atome

23

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Häufig gestellte Fragen

Tetrabenazine is a monoamine-depleting agent that reversibly inhibits vesicular monoamine transporter 2 (VMAT2), blocking the packaging of dopamine, serotonin, and norepinephrine into synaptic vesicles and depleting presynaptic monoamine stores. It is approved for the treatment of chorea associated with Huntington's disease, and is also used for hemiballismus, tardive dyskinesia, and other hyperkinetic movement disorders. Central dopamine depletion reduces involuntary movements but can cause depression, sedation, and parkinsonism as adverse effects.

Yes, Tetrabenazine is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL117785. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6018. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Medizinischer Haftungsausschluss

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.