Weight | 246.266 g/mol |
---|---|
Formula | C13H14N2O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
Mephobarbital (115-38-8)
Mebaral · Methylphenobarbital · Methylphenobarbitone
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- Sigma-Aldrich - Mephobarbital49.00 - 448.35 USD
- Fisher Scientific - Search for Mephobarbital
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- Stereoselective mephobarbital hydroxylation cosegregates with mephenytoin hydroxylation (Clinical Pharmacology & Therapeutics, 1985)
- THE INFLUENCE OF AGE AND GENDER ON THE STEREOSELECTIVE METABOLISM AND PHARMACOKINETICS OF MEPHOBARBITAL IN HUMANS (Clinical Pharmacology & Therapeutics, 1990)
- Polymorphic metabolism of mephenytoin in man: Pharmacokinetic interaction with a co-regulated substrate, mephobarbital (Clinical Pharmacology & Therapeutics, 1986)
- Allyl m-Trifluoromethyldiazirine Mephobarbital: An Unusually Potent Enantioselective and Photoreactive Barbiturate General Anesthetic (Journal of Medicinal Chemistry, 2012)
- Role of human CYP2B6 in S-mephobarbital N-demethylation. (Drug Metabolism and Disposition, 1999)
- Vergleich von verteilung, narkotischer wirksamkeit und metabolischer elimination der optischen antipoden von methylphenobarbital (Biochemical Pharmacology, 1968)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Mebaral
- Methylphenobarbital
- Methylphenobarbitone
- Prominal
- Sanofi Brand of Mephobarbital
- N-Methylphenobarbital
- Sanofi Synthelabo Brand of Mephobarbital
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SMILESCCC1(C(=O)NC(=O)N(C1=O)C)C2=CC=CC=C2
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InChIKeyALARQZQTBTVLJV-UHFFFAOYSA-N
- Pubchem - Mephobarbital
- Wikipedia - mephobarbital
Methylphenobarbital (INN), also known as mephobarbital (USAN, JAN) and mephobarbitone (BAN), marketed under brand names such as Mebaral, Mephyltaletten, Phemiton, and Prominal, is a drug which is a barbiturate derivative and is used primarily as an anticonvulsant, but also as a sedative and anxiolytic. It is the N-methylated analogue of phenobarbital and has similar indications, therapeutic value, and tolerability.
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