Benztropine Mesylate
The mesylate salt form of benztropine, an anticholinergic drug used to relieve Parkinson's symptoms and drug-induced movement disorders. It helps reduce tremor, muscle stiffness, and involuntary movements by blocking certain nerve signals. Common side effects include dry mouth, blurred vision, and constipation.
Молекулярная масса
403,5000 g/mol
TPSA
75,20 Ų
Терапевтические области
Механизм действия
Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.
2D Структура
Cite this structure
Embed this structure
SMILES
CN1[C@@H]2CC[C@H]1C[C@@H](OC(c1ccccc1)c1ccccc1)C2.CS(=O)(=O)O
InChI
InChI=1S/C21H25NO.CH4O3S/c1-22-18-12-13-19(22)15-20(14-18)23-21(16-8-4-2-5-9-16)17-10-6-3-7-11-17;1-5(2,3)4/h2-11,18-21H,12-15H2,1H3;1H3,(H,2,3,4)/t18-,19+,20+;
Molecular Formula
C22H29NO4S
HBD / HBA
1 / 5
Вращаемые Связи
4
Тяжёлые Атомы
28
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.
Часто задаваемые вопросы
The mesylate salt form of benztropine, an anticholinergic drug used to relieve Parkinson's symptoms and drug-induced movement disorders. It helps reduce tremor, muscle stiffness, and involuntary movements by blocking certain nerve signals. Common side effects include dry mouth, blurred vision, and constipation.
Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.
Yes, Benztropine Mesylate 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). CHEMBL1200383. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 238053. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
Медицинский отказ от ответственности
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.
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