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Methocarbamol-d5

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    Methocarbamol-d<sub>5</sub>
  • Methocarbamol-d<sub>5</sub>
Cat No: 33464
Biochemicals - Isotopically Labeled Standards
Cayman

Methocarbamol-d5 is intended for use as an internal standard for the quantification of methocarbamol (Item No. 23870) by GC- or LC-MS. Methocarbamol is an orally bioavailable skeletal muscle relaxant.{38705} In vivo, methocarbamol inhibits the ability...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 3-(2-methoxyphenoxy)-1,2-propane-1,1,2,3,3-d5-diol, 1-carbamate
Correlated keywords:
  • deuterated deuterium GCMS LCMS AHR85 NSC 170960 NSC17960
Product Overview:
Methocarbamol-d5 is intended for use as an internal standard for the quantification of methocarbamol (Item No. 23870) by GC- or LC-MS. Methocarbamol is an orally bioavailable skeletal muscle relaxant.{38705} In vivo, methocarbamol inhibits the ability of mice to remain on a vertical ladder for 1 minute (ED50 = 15 mg/kg) and decreases forelimb grip strength by 35.9% when administered at a dose of 500 mg/kg.{38705,38707} It abolishes femoral nerve-stimulated polysynaptic reflex contractions of the cat tibialis anterior muscle and prolongs the mean refractory period of directly or indirectly stimulated skeletal muscle when administered at a dose of 200 mg/kg.{38708} Methocarbamol also selectively inhibits human carbonic anhydrase (CA) isoform I over CAII (IC50s = 70 and ~80,000 μM, respectively).{38706} Formulations containing methocarbamol have been used to treat skeletal muscle spasms.
Size 500 µg
Shipping dry ice
CAS Number 1189699-70-4
Molecular Formula C11H10D5NO5
SMILES NC(OC([2H])([2H])C(O)([2H])C([2H])([2H])OC1=C(C=CC=C1)OC)=O
Molecular Weight 246,3
Formulation A solid
Purity ≥99% deuterated forms (d1-d5)
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.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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ISO Guide 34:2009

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