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Merck
CN

04141

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
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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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

SMILES string

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

InChI key

YAFGHMIAFYQSCF-UHFFFAOYSA-N

assay

≥99.0% (HPLC)

solubility

DMSO: soluble

fluorescence

λex 324 nm; λem 414 nm in DMSO

suitability

suitable for fluorescence

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.

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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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Microtiter plate assays for inhibition of human, drug-metabolizing cytochromes P450.
C L Crespi et al.
Analytical biochemistry, 248(1), 188-190 (1997-05-15)
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
Clarissa Gerhäuser et al.
Mutation research, 523-524, 163-172 (2003-03-12)
Identification and use of effective cancer chemopreventive agents have become an important issue in public health-related research. For identification of potential cancer chemopreventive constituents we have set up a battery of cell- and enzyme-based in vitro marker systems relevant for
J Martin et al.
The Biochemical journal, 295 ( Pt 1), 73-80 (1993-10-01)
A novel procedure for the isolation of Clara cells from rat lung is described. Single-cell suspensions from male F344/TOX rat lungs, prepared by subtilisin digestion, were treated with monochlorobimane (10 microM) and anlaysed by fluorescence-activated flow cytometry. A sub-population of
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)

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