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Levetiracetam-[2,3,3,4,4,4-butyramide-d6]

General Information
Catalog: BLP-009012
CAS: 1133229-29-4
Molecular Formula: C8H8D6N2O2
Molecular Weight: 176.25
Chemical Structure
Levetiracetam-[2,3,3,4,4,4-butyramide-d6]
Description Levetiracetam-[d3] is an isotope labelled analog of Levetiracetam. Levetiracetam is a medication used to treat epilepsy.
Synonyms (αS)-α-(Ethyl-1,1,2,2,2-d5)-2-oxo-1-pyrrolidineacetamide-α-d; (-)-Levetiracetam-d6
IUPAC Name 2,3,3,4,4,4-hexadeuterio-2-(2-oxopyrrolidin-1-yl)butanamide
Related CAS 102767-28-2 (unlabelled)
Canonical SMILES CCC(C(=O)N)N1CCCC1=O
InChI InChI=1S/C8H14N2O2/c1-2-6(8(9)12)10-5-3-4-7(10)11/h6H,2-5H2,1H3,(H2,9,12)/i1D3,2D2,6D
InChI Key HPHUVLMMVZITSG-CUYPRXAISA-N
Melting Point 116-117°C
Purity 98% by CP; 98% atom D
Solubility Soluble in Acetone, Chloroform, Methanol
Appearance White to Pale Yellow Solid
Storage Store at -20°C, Under inert atmosphere

Levetiracetam-[2,3,3,4,4,4-butyramide-d6], a deuterated variant of the anticonvulsant Levetiracetam, finds primary utility in research settings. Explore its diverse applications:

Pharmacokinetic Studies: Delving into pharmacokinetics, Levetiracetam-[2,3,3,4,4,4-butyramide-d6] serves as a pivotal tool in unraveling the drug's absorption, distribution, metabolism, and excretion profiles. The deuterium labeling facilitates precise monitoring through mass spectrometry, furnishing crucial data to refine dosing strategies and enhance therapeutic outcomes.

Mechanistic Research: Researchers employ Levetiracetam-[2,3,3,4,4,4-butyramide-d6] to probe the intricate mechanisms underpinning its anticonvulsant properties. This compound aids in pinpointing the molecular targets and pathways essential for seizure management. Such profound insights pave the way for the development of advanced anticonvulsant agents with heightened safety margins.

Therapeutic Monitoring: Embracing therapeutic drug monitoring, Levetiracetam-[2,3,3,4,4,4-butyramide-d6] ensures patients attain optimal plasma concentrations for effective seizure management. Leveraging its unique labeling, precise measurement, and differentiation from endogenous metabolites are facilitated. This personalized approach fine-tunes treatment regimens, minimizing adverse effects, and maximizing therapeutic benefits.

Drug Interaction Studies: The deuterated rendition of Levetiracetam assumes a crucial role in probing potential drug interactions. By scrutinizing how concomitant medications modulate the pharmacokinetics of Levetiracetam-[2,3,3,4,4,4-butyramide-d6], researchers predict interactions that may impact drug efficacy or elevate toxicity risks. This valuable intelligence guides the formulation of safer medication combinations for individuals grappling with epilepsy.

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