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Chemodex
7-Ethoxycoumarin
Product Details | |
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Synonyms | 7-Ethoxy-1-benzopyran-2-one; Ethylumbelliferone; 7-ethoxychromen-2-one |
Product Type | Chemical |
Properties | |
Formula | C11H10O3 |
MW | 190.2 |
CAS | 31005-02-4 |
RTECS | DJ3053100 |
Source/Host Chemicals | Synthetic |
Purity Chemicals | ≥98% (GC) |
Appearance | White to light brown powder. |
Solubility | Soluble in ethanol (50 mg/ml) or DMSO (10mg/ml). |
Identity | Determined by 1H-NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | LIFAQMGORKPVDH-UHFFFAOYSA-N |
Smiles | O=C1C=CC2=CC=C(OCC)C=C2O1 |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +20°C |
Long Term Storage | +20°C |
Handling Advice | Protect from light and moisture. |
Use/Stability | Stable for at least 2 years after receipt when stored at RT. |
Documents | |
MSDS | Inquire |
Product Specification Sheet | |
Datasheet | Download PDF |
7-Ethoxycoumarin (7-EC) is a naturally occurring derivative of coumarin that is commonly found in numerous plant species. 7-Ethoxycoumarin is a substrate for cytochrome P450 (CYP450) has been used in the functional characterization of various CYPs. It undergoes O-deethylation by various CYP isoforms, including CYP1A1, -1A2, and -2B in mice and CYP2E1 in humans. Has been used in high-throughput screens in fluorometric p450 activity assays and is metabolized to the fluorescent metabolite 7-Hydroxycoumarin with λex=370nm; λem=450nm. This product can be used as analytical reference compound.
(1) A. Zitting; Anal. Biochem. 115, 177 (1981) | (2) H. Yamazaki, et al.; Biochem. Pharmacol. 51, 313 (1996) | (3) H. Yamazaki, et al.; J. Chromatogr. B Biomed. Sci. Appl. 721, 13 (1999) | (4) T. Shimada, et al.; Drug Metab. Dispos. 27, 1274 (1999) | (5) D.J. Waxman & T.K.H. Chang; Methods Mol. Biol. 320, 153 (2006) | (6) D.H. Kim, et al.; Drug Metab. Dispos. 36, 2166 (2008) | (7) T. Uno, et al.; Biopharm. Drug Dispos. 34, 87 (2013) | (8) W.Y.Feng, et al.; Drug Metab. Lett. 12, 33 (2018)