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Metamizole-d3 (sodium salt)

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    Metamizole-d<sub>3</sub> (sodium salt)
  • Metamizole-d<sub>3</sub> (sodium salt)
Cat No: 26496
Biochemicals - Ion Channel Modulation
Cayman

Metamizole-d3 is intended for use as an internal standard for the quantification of metamizole (Item No. 15771) by GC- or LC-MS. Metamizole is a nonopioid prodrug that is rapidly hydrolyzed to the analgesic and antipyretic metabolites 4-methylaminoant...

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: 1 mg

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • ((1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)(methyl-d3)amino)methanesulfonate, monosodium salt
Correlated keywords:
  • COX CB 1 2 REPV GCMS LCMS Deuterated Deuterium non-opioid TRPV 1 Metamizol Dipirona anti-pyretic TNF? IL6 Lipopolysaccharide
Product Overview:
Metamizole-d3 is intended for use as an internal standard for the quantification of metamizole (Item No. 15771) by GC- or LC-MS. Metamizole is a nonopioid prodrug that is rapidly hydrolyzed to the analgesic and antipyretic metabolites 4-methylaminoantipyrine (MAA) and 4-aminoantipyrine (AA).{25749} It inhibits COX-1 and COX-2 activity (IC50 = ~150 µg/ml for both in cell-free assays), as well as reduces increases in intracellular calcium levels induced by the TRPA1 agonist AITC in isolated rat and mouse dorsal root ganglia and IMR-90 human fibroblasts (IC50s = 30-91 µM in patch-clamp assays).{46639,46640} Metamizole (6, 12, and 25 µg/ml) inhibits ADP- and epinephrine-induced platelet aggregation in human platelet-rich plasma (hPRP).{46641} It prevents fever induced by LPS, TNF-α, and IL-6, but not arachidonic acid (Item Nos. 90010
90010.1
10006607) or prostaglandin E2 (PGE2; Item No. 14010), in rats when administered at a dose of 120 mg/kg.{46642} Metamizole (250 and 500 mg/kg) increases the paw withdrawal threshold in the paw pressure test, indicating analgesic activity, in rat models of carrageenan-induced acute pain and postoperative incision pain.{46643}
Size 1 mg
Shipping dry ice
Molecular Formula C13H13D3N3O4S • Na
SMILES [O-]S(CN(C([2H])([2H])[2H])C1=C(C)N(C)N(C2=CC=CC=C2)C1=O)(=O)=O.[Na+]
Molecular Weight 336,4
Formulation A solid
Purity ≥99% deuterated forms (d1-d3)
Custom Code 3822.19
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

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