Tacrine Hydrochloride
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)
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
Cite this structure
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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
- 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.
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