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| Product | Description | |
|---|---|---|
| Phenobarbital-1-butyric acid | Phenobarbital-1-butyric acid. Group: Biochemicals. Alternative Names: 5-Ethyltetrahydro-2, 4, 6-trioxo-5-phenyl-1 (2H)pyrimidinebutanoic acid. Grades: Purified. CAS No. 73211-20-8. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C16H18N2O5. US Biological Life Sciences. |  Worldwide |
| Phenobarbital 1-Butyric Acid | Phenobarbital derivative. Group: Biochemicals. Grades: Highly Purified. CAS No. 73211-20-8. Pack Sizes: 10mg, 100mg. Molecular Formula: C16H18N2O5, Molecular Weight: 318.32. US Biological Life Sciences. | Worldwide |
| Phenobarbital (AP) | Phenobarbital (AP). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 50U. US Biological Life Sciences. | Worldwide |
| Phenobarbital impurity A | Phenobarbital impurity A. Uses: For analytical and research use. Group: European pharmacopoeia (ph. eur.); pharmacopoeial standards. Alternative Names: 2,6-Diamino-5-ethyl-5-phenyl-4(5H)-Pyrimidinone, Phenobarbital Imp. A (EP). CAS No. 69125-70-8. IUPAC Name: 5-ethyl-2,6-diimino-5-phenyl-1,3-diazinan-4-one. Molecular Formula: C12H14N4O. Mole Weight: 230.27. Catalog: APS69125708. SMILES: CCC1(C(=N)NC(=N)NC1=O)c2ccccc2. Format: Neat. Shipping: Room Temperature. |  |
| Native Rabbit Cytochrome P450 Reductase induced with phenobarbital | The enzyme catalyses electron transfer to cytochrome P450. This system plays a major role in detoxification of drugs and xenobiotics, activation of carcinogens, and metabolism of endogenous substrates such as steroids. Group: Enzymes. Synonyms: EC 1.6.2.4; NADPH:ferrihemoprotein oxidoreductase; NADPH:hemoprotein oxidoreductase; NADPH:P450 oxidoreductase; P450 reductase; CPR; 9039-06-9; FAD-cytochrome c reductase; NADPH-dependent cytochrome c reductase; NADPH:P-450 reductase. Enzyme Commission Number: EC 1.6.2.4. CAS No. 9023-82-9. Purity: ~90% (SDS-PAGE). CPR. Mole weight: mol wt ~80 kDa. Activity: 25-75 units/mg protein (Bradford). Storage: -20°C. Form: buffered aqueous glycerol solution. Solution in 30 mM potassium phosphate buffer, pH 7.7, and 0.1 mM EDTA containing 50% (v/v) glycerol. Source: Rabbit liver. Species: Rabbit. EC 1.6.2.4; NADPH:ferrihemoprotein oxidoreductase; NADPH:hemoprotein oxidoreductase; NADPH:P450 oxidoreductase; P450 reductase; CPR; 9039-06-9; FAD-cytochrome c reductase; NADPH-dependent cytochrome c reductase; NADPH:P-450 reductase. Cat No: NATE-0158. |  |
| N-Methoxymethyl phenobarbital | N-Methoxymethyl phenobarbital. Group: Biochemicals. Alternative Names: 5-Ethyl-1-(methoxymethyl)-5-phenyl- 2,4,6(1H,3H,5H)-pyrimidinetrione; 1-Methoxy methyl phenobarbital; N-Methoxymethyl-5-phenyl-5-ethylbarbituric acid. Grades: Purified. CAS No. 42013-65-0. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C14H16N2O4. US Biological Life Sciences. | Worldwide |
| Eterobarbital | Eterobarbital. Group: Biochemicals. Alternative Names: 5-Ethyl-1,3-bis(methoxymethyl)-5-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione; 1,3-Bis(methoxymethyl)-5-ethyl-5-phenylbarbituric acid; 1, 3-Bis (methoxymethyl) phenobarbital. Grades: Purified. CAS No. 27511-99-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C16H20N2O5. US Biological Life Sciences. | Worldwide |
| Nafenopin | Nafenopin is a hypolipidemic agent, a peroxisome proliferator, on the activities of rat liver glutathione-requiring enzymes and catalase in comparison to the action of phenobarbital. Uses: A hypolipidemic agent. Synonyms: 2-Methyl-2-[4-(1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]propanoic acid. Grades: ≥98%. CAS No. 3771-19-5. Molecular formula: C20H22O3. Mole weight: 310.39. |  |
| 2-Phenylbutyrylurea | 2-Phenylbutyrylurea is used in the synthesis and discovery of novel trypanosomicidal drug-like compounds which is useful in the treatment of diseases. A degradation product of Phenobarbitol (P316760). Group: Biochemicals. Grades: Highly Purified. CAS No. 90-49-3. Pack Sizes: 10mg, 25mg. Molecular Formula: C11H14N2O2. US Biological Life Sciences. | Worldwide |
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