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经验公式(希尔记法):
C12H9NO3
化学文摘社编号:
分子量:
215.20
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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.
signalword
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
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
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)
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
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)
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