1189944-02-2
1189944-02-2
Chemical Structure
Pirenzepine-d8
Synonym(s): LS 519-d8 free base; Pirenzepin-d8; Gastrozepin-d8
- CAS No.: 1189944-02-2
- Formula:C19H13D8N5O2
- Molecular Weight:359.45
IUPAC Name: 11-(2-(4-methylpiperazin-1-yl-2,2,3,3,5,5,6,6-d8)acetyl)-5,11-dihydro-6H-benzo[e]pyrido[3,2-b][1,4]diazepin-6-one
InChIKey: RMHMFHUVIITRHF-PMCMNDOISA-N
SMILES: O=C1NC2=CC=CN=C2N(C(CN3C([2H])([2H])C([2H])([2H])N(C)C([2H])([2H])C3([2H])[2H])=O)C4=CC=CC=C14
Biological Activity: Pirenzepine-d8 is the deuterium labeled Pirenzepine dihydrochloride. Pirenzepine dihydrochloride (LS519) is a selective M1 muscarinic receptor antagonist.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Pirenzepine-d8 | Pirenzepine-d8 is the deuterium labeled Pirenzepine dihydrochloride. Pirenzepine dihydrochloride (LS519) is a selective M1 muscarinic receptor antagonist. | |||||||||||||||||||||
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Pirenzepine dihydrochloride (Standard) | ≥98% | Pirenzepine (dihydrochloride) (Standard) is the analytical standard of Pirenzepine (dihydrochloride). This product is intended for research and analytical applications. Pirenzepine (LS 519) dihydrochloride is a selective M1 mAChR (muscarinic acetylcholine receptor) antagonist. Pirenzepine dihydrochloride reduces gastric acid secretion and reduces muscle spasm, can be used in peptic ulcers research. Pirenzepine dihydrochloride shows anti-proliferative activity to cancer cells. | ||||||||||||||||||||
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Pirenzepine-d8 dihydrochloride | Pirenzepine-d8 (LS 519-d8; Pirenzepin-d8) dihydrochloride is a deuterium labeled Pirenzepine (dihydrochloride) (HY-17037). Pirenzepine (LS 519) dihydrochloride is a selective M1 mAChR (muscarinic acetylcholine receptor) antagonist. Pirenzepine dihydrochloride reduces gastric acid secretion and reduces muscle spasm, can be used in peptic ulcers research. Pirenzepine dihydrochloride shows anti-proliferative activity to cancer cells. | |||||||||||||||||||||
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Pirenzepine dihydrochloride | 99.84% | Pirenzepine (LS 519) dihydrochloride is a selective M1 mAChR (muscarinic acetylcholine receptor) antagonist, with poor penetration of the blood-brain barrier. Pirenzepine dihydrochloride reduces gastric acid secretion and reduces muscle spasm, can be used in peptic ulcers research. Pirenzepine dihydrochloride shows anti-proliferative activity to cancer cells. | ||||||||||||||||||||
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