Bethanechol Chloride
The chloride salt form of bethanechol, used to treat non-obstructive urinary retention and neurogenic bladder by stimulating muscle contractions. It acts on muscarinic receptors to promote bladder emptying and may also be used for certain gastrointestinal motility issues. Side effects can include abdominal cramps, sweating, and low blood pressure.
Khối lượng phân tử
196,6700 g/mol
TPSA
52,30 Ų
Lĩnh vực điều trị
Cơ chế tác dụng
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.
Cấu trúc 2D
Cite this structure
Embed this structure
SMILES
CC(C[N+](C)(C)C)OC(N)=O.[Cl-]
InChI
InChI=1S/C7H16N2O2.ClH/c1-6(11-7(8)10)5-9(2,3)4;/h6H,5H2,1-4H3,(H-,8,10);1H
Molecular Formula
C7H17ClN2O2
HBD / HBA
1 / 3
Liên kết có thể quay
4
Nguyên tử nặng
12
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.
Câu hỏi thường gặp
The chloride salt form of bethanechol, used to treat non-obstructive urinary retention and neurogenic bladder by stimulating muscle contractions. It acts on muscarinic receptors to promote bladder emptying and may also be used for certain gastrointestinal motility issues. Side effects can include abdominal cramps, sweating, and low blood pressure.
Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.
Yes, Bethanechol Chloride 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). CHEMBL1768. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 11548. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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