N-desmethyl pirenzepine-D8

Product Name N-desmethyl pirenzepine-D8
Alternate Names Pirenzepine Stable Isotopes, Stable Isotopes of Pirenzepine
CAT No. CS-O-15704
CAS No. 1189860-05-6
Category Stable Isotopes
Stock Enquire
Mol. Wt. 345.43 g/mol
Mol. For. C₁₈H₁₁D₈N₅O₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Pirenzepine
Purity >98
Therapeutic Anti ulcer
Smileys C1CN(CCN1)CC(=O)N2C3=CC=CC=C3C(=O)NC4=C2N=CC=C4
Canonical Smiles C1CN(CCN1)CC(=O)N2C3=CC=CC=C3C(=O)NC4=C2N=CC=C4
InchIKey FSKGDOFJFMYNIG-JNJBWJDISA-N
Inchl InChI=1S/C18H19N5O2/c24-16(12-22-10-8-19-9-11-22)23-15-6-2-1-4-13(15)18(25)21-14-5-3-7-20-17(14)23/h1-7,19H,8-12H2,(H,21,25)/i8D2,9D2,10D2,11D2
IUPAC 11-[2-(2,2,3,3,5,5,6,6-octadeuteriopiperazin-1-yl)acetyl]-5H-pyrido[2,3-b][1,4]benzodiazepin-6-one
Controlled No
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N-desmethyl pirenzepine-D8 is a deuterated form of N-desmethyl pirenzepine, which is a muscarinic receptor antagonist used in medical research. Muscarinic receptors are a type of acetylcholine receptor found in the central and peripheral nervous systems, and they play a role in various physiological processes such as regulation of heart rate, smooth muscle contraction, and neurotransmitter release. The use of N-desmethyl pirenzepine-D8 in research allows for the determination of the pharmacokinetics and metabolism of the non-deuterated compound, as well as the identification of potential drug interactions and mechanisms of action. Chemically, N-desmethyl pirenzepine-D8 is a deuterated derivative of N-desmethyl pirenzepine, with eight deuterium atoms replacing eight hydrogen atoms. This substitution results in a slight increase in molecular weight and a shift in the mass spectrum, making it useful for mass spectrometry-based analysis. The compound is typically administered intravenously or orally in animal studies, and its effects are evaluated through various assays such as binding studies, behavioral tests, and electrophysiology. Overall, N-desmethyl pirenzepine-D8 is a valuable tool for researchers studying muscarinic receptors and their associated physiological processes. Its deuterated form allows for more precise analysis and understanding of the pharmacokinetics and metabolism of the non-deuterated compound, as well as potential drug interactions and mechanisms of action.

Related Compounds

Pirenzepine D8 Dihydrochloride |

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