Pirenzepine
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Systematic (IUPAC) name | |
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11-[(4-methylpiperazin-1-yl)acetyl]-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one
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Clinical data | |
AHFS/Drugs.com | monograph |
Identifiers | |
CAS Number | 28797-61-7 Y |
ATC code | A02BX03 (WHO) |
PubChem | CID: 4848 |
IUPHAR/BPS | 328 |
DrugBank | DB00670 Y |
ChemSpider | 4682 Y |
UNII | 3G0285N20N Y |
KEGG | D08389 Y |
ChEBI | CHEBI:8247 Y |
ChEMBL | CHEMBL9967 Y |
Chemical data | |
Formula | C19H21N5O2 |
Molecular mass | 351.403 g/mol |
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Pirenzepine (Gastrozepin), an M1 selective antagonist, 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.[1] 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.[2][3]
See also
References
H2 antagonists ("-tidine") | |
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Prostaglandins (E)/analogues ("-prost-") | |
Proton-pump inhibitors ("-prazole") | |
Potassium-competitive acid blockers ("-prazan") | |
Others | |
Combinations | |
Simple piperazines (no additional rings) |
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Phenylpiperazines |
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Benzylpiperazines | |
Diphenylalkylpiperazines (benzhydrylalkylpiperazines) |
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Pyrimidinylpiperazines | |
Pyridinylpiperazines | |
Benzo(iso)thiazolylpiperazines | |
Tricyclics (piperazine attached via side chain) |
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Others/Uncategorized |
Classes | |
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Antidepressants (TCAs and TeCAs) |
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Antihistamines |
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Antipsychotics |
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Anticonvulsants | |
Others |
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