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C2612

Sigma-Aldrich

3-Cyano-7-ethoxycoumarin

≥90% (at 254 nm, HPLC)

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About This Item

Fórmula empírica (notación de Hill):
C12H9NO3
Número de CAS:
117620-77-6
Peso molecular:
215.20
MDL number:
MFCD00467359
UNSPSC Code:
12161501
PubChem Substance ID:
24724435

description

Light sensitive

assay

≥90% (at 254 nm, HPLC)

form

powder

solubility

DMSO: soluble

fluorescence

λem 411 nm (+/- 4nm)

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

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Biochem/physiol Actions

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

pictograms

Exclamation mark
GHS07

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_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

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Abeer ElKhoely et al.
Journal of natural medicines, 69(3), 313-323 (2015-03-23)
Liver cancer is the fifth commonest malignancy worldwide and the third leading cause of death. Identifying novel curative and preventive therapy may improve its prognosis. In this study, thymoquinone (TQ), the most active biological ingredient of Nigella sativa Linn, was
Kathleen W Mosure et al.
Journal of pharmaceutical sciences, 104(9), 2813-2823 (2015-01-30)
Asunaprevir (ASV; BMS-650032), a low nanomolar inhibitor of the hepatitis C virus (HCV) NS3 protease, is currently under development, in combination with other direct-acting antiviral (DAA) agents for the treatment of chronic HCV infection. Extensive nonclinical and pharmacokinetic studies have
Therese Ericsson et al.
Xenobiotica; the fate of foreign compounds in biological systems, 44(7), 615-626 (2014-01-10)
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
Roslyn Thelingwani et al.
Expert opinion on drug metabolism & toxicology, 10(10), 1313-1324 (2014-09-16)
Drug resistance by Plasmodium falciparum remains a challenge in malaria chemotherapy. This paper will focus on physicochemical and drug metabolism characterization of a series of 4-aminoquinoline-3-hydroxypyridin-4-one hybrid shown to have antimalarial activity against chloroquine-resistant P. falciparum. The aim is to

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