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rac O-Desmethyl Naproxen-[d3]

General Information
Catalog: BLP-013087
CAS: 1122399-99-8
Molecular Formula: C13H9D3O3
Molecular Weight: 219.25
Chemical Structure
rac O-Desmethyl Naproxen-[d3]
Description rac O-Desmethyl Naproxen-[d3] is the labelled analogue of rac O-Desmethyl Naproxen, which is a metabolite of Naproxen, a non-steroidal anti-inflammatory agent.
Synonyms rac O-Desmethyl Naproxen D3; 6-Hydroxy-α-(methyl-d3)-2-naphthaleneacetic Acid; 2-(6-Hydroxy-2-naphthyl)propionic Acid-d3; 6-O-Desmethylnaproxen-d3; Demethylnaproxen-d3; (±)-O-Desmethyl Naproxen-d3 (α-methyl-d3)
IUPAC Name 3,3,3-trideuterio-2-(6-hydroxynaphthalen-2-yl)propanoic acid
Related CAS 60756-73-2 (unlabelled)
Isomeric SMILES [2H]C([2H])([2H])C(C1=CC2=C(C=C1)C=C(C=C2)O)C(=O)O
Canonical SMILES CC(C1=CC2=C(C=C1)C=C(C=C2)O)C(=O)O
InChI InChI=1S/C13H12O3/c1-8(13(15)16)9-2-3-11-7-12(14)5-4-10(11)6-9/h2-8,14H,1H3,(H,15,16)/i1D3
InChI Key XWJUDDGELKXYNO-FIBGUPNXSA-N
Melting Point >172°C (dec.)
Purity 95% by HPLC; 98% atom D
Solubility Soluble in DMSO, Methanol
Appearance Dark Red Solid
Storage Store at -20°C

rac O-Desmethyl Naproxen-[d3], a stable isotope-labeled compound utilized primarily in biomedical research, has diverse applications. Here are the key applications:

Pharmacokinetics Studies: Delving into the realm of pharmacokinetics, rac O-Desmethyl Naproxen-[d3] emerges as a pivotal tool for exploring the dynamics of Naproxen and its metabolites within the human body. By tracing the labeled compound in various biological samples, researchers unlock insights into absorption, distribution, metabolism, and excretion (ADME) pathways. This understanding sheds light on the intricate behavior of drugs and aids in the optimization of dosing protocols.

Metabolomics: In the intricate landscape of metabolomics research, rac O-Desmethyl Naproxen-[d3] assumes a crucial role as an internal standard, enabling the precise quantification of Naproxen metabolites with impeccable accuracy. Its utilization guarantees reproducible measurements in complex biological matrices like blood, urine, and tissue samples. This precision is pivotal in unveiling metabolic alterations linked to diseases or therapeutic interventions, paving the way for a deeper understanding of physiological changes.

Drug Interaction Studies: Featuring prominently in drug-drug interaction investigations, rac O-Desmethyl Naproxen-[d3] facilitates the exploration of how Naproxen and its metabolites interact with other pharmaceutical agents. Harnessing the power of the labeled compound, scientists can pinpoint and quantify these interactions with exceptional sensitivity. This knowledge is paramount in mitigating adverse reactions and enhancing the therapeutic efficacy of drug regimens, underscoring the importance of comprehensive drug interaction assessments.

Analytical Method Development: Serving as a cornerstone in the realm of analytical method development, rac O-Desmethyl Naproxen-[d3] plays a pivotal role in crafting and validating techniques for the detection and quantification of Naproxen and its metabolites. Its integration into methodologies like liquid chromatography-mass spectrometry (LC-MS) elevates accuracy and sensitivity, setting the stage for robust and reliable analytical approaches. These validated methods are indispensable for ensuring regulatory compliance and upholding stringent quality control standards in pharmaceutical research and development.

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