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Referencia número: HY-111177R

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Pheneturide (Standard)

Name: Pheneturide (Standard)
Brand: MedChemExpress
SKU: HY-111177R
Price: 100.00 USD
Availability: InStock
Rating: 5 (1 reviews)

(Synonyms: Ethylphenacemide (Standard); M 551 (Standard))

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Pheneturide (Ethylphenacemide; M 551) (Standard) is the analytical standard of Pheneturide (HY-111177). This product is intended for research and analytical applications. Pheneturide (Ethylphenacemide; M 551) is an orally active anticonvulsant. Pheneturide is a decarboxylation product of 5-ethyl-5-phenylbarbituric acid, with antiepileptic and central inhibitory effects. Pheneturide has protective effects against both MES tonic convulsions and Metrazol clonic convulsions. Pheneturide prolongs sedative-induced sleep, increases spontaneous locomotor activity, and inhibits fighting behavior. Pheneturide can be used in epilepsy-related research.

Para uso exclusivo en investigación. No vendemos a pacientes.

Pureza : 99.84%
No. CAS: 90-49-3
Fòrmula: C₁₁H₁₄N₂O₂
Peso molecular:206.24

Almacenamiento:

Please store the product under the recommended conditions in the Certificate of Analysis.

Pheneturide (Standard) Chemical Structure

No. CAS: 90-49-3

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Information

Aplicación

The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.

Chemical Information

No. CAS 90-49-3
Appearance Solid
Peso molecular 206.24
Fòrmula C₁₁H₁₄N₂O₂
Color White to off-white
SMILES

O=C(NC(N)=O)C(CC)C1=CC=CC=C1
Synonyms

Ethylphenacemide (Standard); M 551 (Standard)
Envío

Room temperature in continental US; may vary elsewhere.
Almacenamiento

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureza y Documentación

Select Batch:

Pureza: 99.98%

Assay: 99.98%

ee.: 99.98%

SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
COA (2659 KB)
Instrucciones de manejo (2659 KB)

Referencias

[1]. 中村圭二, et al. THE ANTICONVULSANT ACTIVITY OF ETHYL α-PHENYLBUTYROYL ALLOPHANATE (P-5257). The Japanese Journal of Pharmacology. 1963;13(3):259-73.

[2]. Swinyard EA. Acetylurea derivatives. InAntiepileptic Drugs 1985 (pp. 601-610). Berlin, et al.

[3]. Morton DJ. Effect of anticonvulsant drugs in vivo on rat pineal N‐acetyltransferase (EC 2.3. 1.5) and hydroxyindole‐O‐methyltransferase (EC 2.1. 1.4). Journal of pineal research. 1986 Apr;3(2):181-6.

[4]. Mandel HG, et al. Interference of barbiturates with pyrimidine incorporation—II: Structural specificity of the inhibition of orotate uptake inBacillus cereus. Biochemical Pharmacology. 1970 Jun 1;19(6):1867-77.

[5]. Masuda Y, et al. Differential antagonisms of anticonvulsants to various components of maximal seizures induced by electroshock or pentylenetetrazol in mice. Journal of pharmacobio-dynamics. 1980 Oct;3(10):526-31.

Calculators

Calculadora de molaridad

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculadora de dilución

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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Pheneturide (Standard)

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Pheneturide (Standard)

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Chemical Information

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Referencias

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Pheneturide (Standard) Related Classifications

HY-111177R Related Classifications

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