| Weight | 158.204 g/mol |
|---|---|
| Formula | C10H10N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
1-Benzylimidazole (4238-71-5)
N-benzylimidazole
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- N-benzylimidazole, a high magnitude inducer of rat hepatic cytochrome P-450 exhibiting both polycyclic aromatic hydrocarbon- and phenobarbital-type induction of phase I and phase II drug-metabolizing enzymes. (Drug Metabolism and Disposition, 1988)
- The structure of a monomeric oxygen carrying cobalt complex: dioxygen-N,N'-(1,1,2,2-tetramethyl)ethylenebis(3-tert-butylsalicylideniminato)(1-benzylimidazole)cobalt(II) (Journal of the American Chemical Society, 1976)
- Substituted 1-benzylimidazole-2-thiols as potent and orally active inhibitors of dopamine .beta.-hydroxylase (Journal of Medicinal Chemistry, 1986)
- Tin(IV) and organotin(IV) complexes containing mono or bidentate N-donor ligands-I. 1-Benzylimidazole derivatives. (Polyhedron, 1996)
- Induction of CYP1A by the N-imidazole derivative, 1-benzylimidazole (Environmental Toxicology and Chemistry, 2003)
- N-benzylimidazole carboxamides as potent, orally active stearoylCoA desaturase-1 inhibitors. (Bioorganic & Medicinal Chemistry Letters, 2011)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - N-benzylimidazole
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SMILESC1=CC=C(C=C1)CN2C=CN=C2
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InChIKeyKKKDZZRICRFGSD-UHFFFAOYSA-N
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