87-05-8
87-05-8
Chemical Structure
7-Ethoxy-4-methylcoumarin
- CAS No.: 87-05-8
- Formula:C12H12O3
- Molecular Weight:204.22
IUPAC Name: 7-ethoxy-4-methyl-2H-chromen-2-one
InChIKey: NKRISXMDKXBVRJ-UHFFFAOYSA-N
SMILES: O=C1C=C(C)C2=CC=C(OCC)C=C2O1
Biological Activity: 7-Ethoxy-4-methylcoumarin is a coumarin derivative and can be used as a substrate probe of mammalian cytochromes P450 1A1, 2B4 and 2B6[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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7-Ethoxy-4-methylcoumarin | 99.44% | 7-Ethoxy-4-methylcoumarin is a coumarin derivative and can be used as a substrate probe of mammalian cytochromes P450 1A1, 2B4 and 2B6. | ||||||||||||||||||||
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7-Ethoxy-4-methylcoumarin (Standard) | ≥98% | 7-Ethoxy-4-methylcoumarin (Standard) is the analytical standard of 7-Ethoxy-4-methylcoumarin. This product is intended for research and analytical applications. 7-Ethoxy-4-methylcoumarin is a coumarin derivative and can be used as a substrate probe of mammalian cytochromes P450 1A1, 2B4 and 2B6. | ||||||||||||||||||||
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References
- [1]. Kuhn UD, et al. Induction of cytochrome P450 1A1 in rat liver slices by 7-ethoxycoumarin and 4-methyl-7-ethoxycoumarin. Exp Toxicol Pathol. 1998 Sep;50(4-6):491-6. [Content Brief]
- [2]. Liu J, et al. Coumarin Derivatives as Substrate Probes of Mammalian Cytochromes P450 2B4 and 2B6: Assessing the Importance of 7-Alkoxy Chain Length, Halogen Substitution, and Non-Active Site Mutations. Biochemistry. 2016 Apr 5;55(13):1997-2007. [Content Brief]
