Pirenzepine
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| Systematic (IUPAC) name | |
|---|---|
| 11-[(4-methylpiperazin-1-yl)acetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one | |
| Clinical data | |
| AHFS/Drugs.com | monograph |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 28797-61-7 |
| ATC code | A02BX03 |
| PubChem | CID 4848 |
| IUPHAR ligand | 328 |
| DrugBank | APRD00515 |
| ChemSpider | 4682 |
| UNII | 3G0285N20N |
| KEGG | D08389 |
| ChEBI | CHEBI:8247 |
| ChEMBL | CHEMBL9967 |
| Chemical data | |
| Formula | C19H21N5O2 |
| Mol. mass | 351.403 g/mol |
| SMILES | eMolecules & PubChem |
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Pirenzepine (Gastrozepin) is used in the treatment of peptic ulcers, as it reduces gastric acid secretion and reduces muscle spasm. It is in a class of drugs known as muscarinic receptor antagonists - acetylcholine being the neurotransmitter of the parasympathetic nervous system which initiates the rest-and-digest state (as opposed to fight-or-flight), the result being an increase in gastric motility and digestion. It has no effects on the brain and spinal cord as it cannot diffuse through the blood-brain barrier.
Pirenzepine has been investigated for use in myopia control.[1]
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