Dofetilide D4

Product Name Dofetilide D4
Alternate Names Dofetilide Stable Isotopes, Stable Isotopes of Dofetilide
CAT No. CS-O-03497
CAS No. 1189700-56-8
Category Stable Isotopes
Stock IN-Stock
Mol. Wt. 445.59 g/mol
Mol. For. C₁₉H₂₃D₄N₃O₅S₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Dofetilide
Purity 95%
Smileys CN(CCC1=CC=C(C=C1)NS(=O)(=O)C)CCOC2=CC=C(C=C2)NS(=O)(=O)C
Canonical Smiles CN(CCC1=CC=C(C=C1)NS(=O)(=O)C)CCOC2=CC=C(C=C2)NS(=O)(=O)C
InchIKey IXTMWRCNAAVVAI-QZPARXMSSA-N
Inchl InChI=1S/C19H27N3O5S2/c1-22(13-12-16-4-6-17(7-5-16)20-28(2,23)24)14-15-27-19-10-8-18(9-11-19)21-29(3,25)26/h4-11,20-21H,12-15H2,1-3H3/i14D2,15D2
IUPAC N-[4-[2-[methyl-[1,1,2,2-tetradeuterio-2-[4-(methanesulfonamido)phenoxy]ethyl]amino]ethyl]phenyl]methanesulfonamide
Controlled No
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Dofetilide D4 is a deuterated version of the antiarrhythmic drug Dofetilide, which is commonly used to treat atrial fibrillation and atrial flutter. The deuterated version of the drug is used in research studies to help identify and track the drug's metabolic pathway and to study its pharmacokinetics. Dofetilide D4 works by blocking the potassium ion channels in the heart muscle cells, which slows down the electrical activity in the heart and helps to restore normal heart rhythm. The drug is administered orally and is rapidly absorbed by the body, with peak plasma concentrations reached within two to three hours of ingestion. The drug is metabolized primarily by the liver and eliminated from the body via the kidneys. The deuterated version of Dofetilide, Dofetilide D4, is useful in studies where the metabolic pathway of the drug needs to be tracked. Deuterium is a stable isotope of hydrogen, and its incorporation into the drug molecule allows researchers to identify specific breakdown products of the drug in the body. This information can be used to better understand the drug's pharmacokinetics and to optimize dosing regimens. In conclusion, Dofetilide D4 is a useful tool for researchers studying the pharmacokinetics and metabolic pathways of the antiarrhythmic drug Dofetilide. Its incorporation of deuterium allows for more precise tracking of the drug's breakdown products, which can be used to optimize dosing regimens and improve treatment outcomes for patients with atrial fibrillation and atrial flutter.

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