Induces various cytochrome P-450 isozymes including lauric acid hydroxylase. Decreases plasma triglyceride levels in rats. Inhibits thromboxane A2 synthase.
Product Specification
| Formula: | C10H10N2 |
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| MW: | 158.2 |
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| CAS: | 4238-71-5 |
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| Purity: | ≥97% (GC, Titration) |
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| Appearance: | White solid. |
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| Solubility: | Soluble in DMSO or ethanol. |
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| Shipping: | Ambient |
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| Long Term Storage: | Ambient |
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| Regulatory Status: | RUO - Research Use Only |
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Product Literature References
Involvement of testosterone in the induction of hepatic microsomal cytochrome P-450 2B1/2 (P-450 2B1/2) by 1-benzylimidazole in male and female rats: sex-differentiated induction of P-450 2B1/2 species: Y. Kobayashi, et al.; Biochim. Biophys. Acta.
1200, 11 (1994),
Abstract;
N-benzylimidazole, a potent inducer of rat liver enzymes involved in mutagenic activation of various carcinogens: Y. Mori, et al.; Mutat. Res.
302(2), 129 (1993),
Abstract;
Effect of 1-benzylimidazole on cytochromes P-450 induction and on the activities of epoxide hydrolases and UDP-glucuronosyltransferases in rat liver: J. Magdalou, et al.; Biochem. Pharmacol.
37, 3297 (1988),
Abstract;
Carbon tetrachloride-induced eicosanoid synthesis and enzyme release from rat peritoneal leucocytes: T. J. Lynch, et al.; Biochem. Pharmacol.
34, 1515 (1985),
Abstract;
