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Merck
CN

C2612

3-Cyano-7-ethoxycoumarin

≥90% (at 254 nm, HPLC)

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About This Item

Empirical Formula (Hill Notation):
C12H9NO3
CAS Number:
Molecular Weight:
215.20
UNSPSC Code:
12161501
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

description

Light sensitive

assay

≥90% (at 254 nm, HPLC)

form

powder

solubility

DMSO: soluble

fluorescence

λem 411 nm (+/- 4nm)

Quality Level

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Biochem/physiol Actions

Fluorescent probe useful in microsomal dealkylase studies.
Fluorescent probe useful in microsomal dealkylase studies. Typical drug-drug interactions resulting from enzyme inhibition.

pictograms

Exclamation mark

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Therese Ericsson et al.
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1. Cytochrome P450 enzyme system is the most important contributor to oxidative metabolism of drugs. Modification, and more specifically inhibition, of this system is an important determinant of several drug-drug interactions (DDIs). 2. Effects of the antimalarial agent artemisinin and

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