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Felbamate-d4

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    Felbamate-d<sub>4</sub>
  • Felbamate-d<sub>4</sub>
Cat No: 28489
Biochemicals - Ion Channel Modulation
Cayman

Felbamate-d4 is intended for use as an internal standard for the quantification of felbamate (Item No. 18000) by GC- or LC-MS. Felbamate is an inhibitor of NMDA receptors and a modulator of GABAA receptors that also has broad-spectrum inhibitory activ...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 2-phenyl-1,3-propane-1,1,3,3-d4-diol dicarbamate
Correlated keywords:
  • deuterated deuterium GABA ?1 ?2 ?2S ?3 ?2 Xenopus ?2L ?4 ?6 ADD-03055 ADD03055
Product Overview:
Felbamate-d4 is intended for use as an internal standard for the quantification of felbamate (Item No. 18000) by GC- or LC-MS. Felbamate is an inhibitor of NMDA receptors and a modulator of GABAA receptors that also has broad-spectrum inhibitory activity against excitatory amino acid receptors.{45398,45399,45400} It binds to NMDA channels with dissociation constants of approximately 200, 110, and 55 µM in the resting, activated, and desensitized states, respectively, and inhibits NMDA currents in a use-dependent manner.{45398} Felbamate is a positive modulator of α1β2γ2S, α1β3γ2S, α2β2γ2S, and α2β3γ2S subunit-containing GABAA receptors expressed in X. laevis oocytes, with negative modulation of GABAA receptors containing the subunits α1β1, α1β3γ2L, α4β1γ2S, α4β3γ2S, and α6β1γ2S.{45399} It inhibits seizures induced by maximal electroshock, pentylenetetrazole (Item No. 18682), and picrotoxin (Item No. 20771) in mice (ED50s = 16.3, 5.51, and 5.23 mg/kg, respectively). Formulations containing felbamate have been used in the treatment of severe refractory seizures.
Size 500 µg
Shipping dry ice
CAS Number 106817-52-1
Molecular Formula C11H10D4N2O4
SMILES NC(OC([2H])([2H])C(C([2H])([2H])OC(N)=O)C1=CC=CC=C1)=O
Molecular Weight 242,3
Formulation A solid
Purity ≥99% deuterated forms (d1-d4)
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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