Tacrine Hydrochloride

CHEMBL1677 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
234.7 g/mol
LogP
Phase
4

Tacrine hydrochloride is the hydrochloride salt form of tacrine, a first-generation acetylcholinesterase inhibitor used for Alzheimer's disease that has been largely replaced due to significant hepatotoxicity. See tacrine for complete pharmacological details.

Molekularmasse

234,7200 g/mol

TPSA

38,90 Ų

Therapeutische Bereiche

Wirkmechanismus

Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.

2D-Struktur

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SMILES

Cl.Nc1c2c(nc3ccccc13)CCCC2

InChI

InChI=1S/C13H14N2.ClH/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13;/h1,3,5,7H,2,4,6,8H2,(H2,14,15);1H

Molecular Formula

C13H15ClN2

HBD / HBA

2 / 2

Rotierbare Bindungen

0

Schwere Atome

16

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

Tacrine hydrochloride is the hydrochloride salt form of tacrine, a first-generation acetylcholinesterase inhibitor used for Alzheimer's disease that has been largely replaced due to significant hepatotoxicity. See tacrine for complete pharmacological details.

Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.

Yes, Tacrine Hydrochloride 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). CHEMBL1677. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 2723754. 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.