Chemodex

7-Ethoxycoumarin

CHF 39.00
In stock
CDX-E0252-M100100 mgCHF 39.00
CDX-E0252-M500500 mgCHF 116.00
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Product Details
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
Our product description may differ slightly from the original manufacturers 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
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Product Specification Sheet
Datasheet Download PDF
Description

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.

Product References

(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)

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