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Merck
CN

04141

Sigma-Aldrich

7-Ethoxycoumarin-3-carbonitrile

≥99.0% (HPLC), suitable for fluorescence

Synonym(s):

3-Cyano-7-ethoxycoumarin

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About This Item

Empirical Formula (Hill Notation):
C12H9NO3
CAS Number:
Molecular Weight:
215.20
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
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Assay

≥99.0% (HPLC)

solubility

DMSO: soluble

fluorescence

λex 324 nm; λem 414 nm in DMSO

suitability

suitable for fluorescence

SMILES string

CCOc1ccc2C=C(C#N)C(=O)Oc2c1

InChI

1S/C12H9NO3/c1-2-15-10-4-3-8-5-9(7-13)12(14)16-11(8)6-10/h3-6H,2H2,1H3

InChI key

YAFGHMIAFYQSCF-UHFFFAOYSA-N

Application

This reagent is a fluorogenic substrate suitable for the continuous determination of cytochrome P450 mixed-function monooxygenases. The product of the reaction is the fluorescent compound 3-cyano-7-hydroxycoumarin (Product No. C 2737). This property has been utilized to determine the activity of CYP1A by measuring the rate of dealkylation of 3-Cyano-7-ethoxycoumarin to this fluorescent product . Fluorescence of 3-cyano-7-hydroxycoumarin occurs at neutral pH with excitation and emission at 408 and 450 nm, respectively . Fluorescent reaction product detection is at least 50-fold more sensitive than that of the product of alkyl resorufin oxidation because of greater rate of turnover of 3-Cyano-7-ethoxycoumarin . The ability to continuously monitor the enzyme reaction at pH 7 is derived from the lower pKa of the 3-cyano-7- hydroxycoumarin product compared to that for 7-ethoxycoumarin . 3-Cyano-7-ethoxycoumarin is a suitable substrate for three of the five principal cytochrome P450 drug metabolizing enzymes, CYP1A1, CYP1A2, CYP2C9, and CYP2C19 . It has been used to measure cytochrome P450 mixed-function monooxygenases in rat hepatic microsomal preparations as well as in isolated rat hepatocytes . It was part of a study to examine the expression of CYP2B6 in human liver microsomes, and has been used to characterize Clara and type II cells from rat lung.

Pictograms

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Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Huijuan Wang et al.
Xenobiotica; the fate of foreign compounds in biological systems, 41(9), 826-835 (2011-06-23)
To comprehensively understand the effects of CYP2C19 genetic polymorphisms on inhibition-based drug-drug interactions (DDIs), 18 human CYP2C19 non-synonymous single-nucleotide polymorphic variants and the wild-type isoform (CYP2C19.1A) were expressed in yeast cells. Using a fluorescence-based high-throughput method, the kinetic constants of
David M Stresser et al.
Drug metabolism and disposition: the biological fate of chemicals, 30(7), 845-852 (2002-06-18)
We have tested a panel of 29 cDNA-expressed rat and human enzymes with 9 fluorometric substrates to determine the P450 isoform selectivity in the catalysis of the substrates to fluorescent products. The substrates examined were dibenzyl fluorescein, 7-benzyloxyquinoline (BQ), 3-cyano-7-ethoxycoumarin
The O-dealkylation of 7-ethoxycoumarin by liver microsomes. A direct fluorometric test.
V Ullrich et al.
Hoppe-Seyler's Zeitschrift fur physiologische Chemie, 353(7), 1171-1177 (1972-07-01)
A sensitive liquid chromatographic assay of ethoxycoumarin deethylase with fluorescence detection.
A Zitting
Analytical biochemistry, 115(1), 177-180 (1981-07-15)
I N White et al.
The Biochemical journal, 247(1), 23-28 (1987-10-01)
The formation of ethoxyfluorescein and fluorescein from diethoxyfluorescein by isolated rat hepatocytes has been used as a basis for separating such cells dependent on their mixed function oxidase activities by fluorescence-activated flow cytometry. Five equal fractions defined by computer-generated regions

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