Tacrine Hydrochloride

CHEMBL1677 Phase 4 已批准 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.

分子量

234.7200 g/mol

TPSA

38.90 Ų

治疗领域

作用机制

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)

机制

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

二维结构

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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

可旋转键数

0

重原子数

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.

常见问题

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.

医疗免责声明

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.