Benzgalantamine Gluconate
The gluconate salt form of benzgalantamine, a galantamine prodrug that provides sustained release of the active acetylcholinesterase inhibitor.
分子量
587.6000 g/mol
TPSA
186.00 Ų
作用機序
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.
2D構造
Cite this structure
Embed this structure
SMILES
COc1ccc2c3c1O[C@H]1C[C@@H](OC(=O)c4ccccc4)C=C[C@@]31CCN(C)C2.O=C(O)C(O)C(O)C(O)C(O)CO
InChI
InChI=1S/C24H25NO4.C6H12O7/c1-25-13-12-24-11-10-18(28-23(26)16-6-4-3-5-7-16)14-20(24)29-22-19(27-2)9-8-17(15-25)21(22)24;7-1-2(8)3(9)4(10)5(11)6(12)13/h3-11,18,20H,12-15H2,1-2H3;2-5,7-11H,1H2,(H,12,13)/t18-,20-,24-;/m0./s1
Molecular Formula
C30H37NO11
HBD / HBA
6 / 12
回転可能結合数
9
重原子数
42
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.
よくある質問
The gluconate salt form of benzgalantamine, a galantamine prodrug that provides sustained release of the active acetylcholinesterase inhibitor.
Inhibits acetylcholinesterase, the enzyme that hydrolyzes acetylcholine in the synaptic cleft. This increases acetylcholine availability at cholinergic synapses, enhancing cholinergic neurotransmission.
Yes, Benzgalantamine Gluconate 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). CHEMBL6068431. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 155491118. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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