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Merck

46121

Sigma-Aldrich

Resorufinethylether

suitable for fluorescence, ≥95% (UV)

Synonym(e):

7-Ethoxy-3H-phenoxazin-3-on, Ethoxyresorufin, O7-Ethylresorufin

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About This Item

Empirische Formel (Hill-System):
C14H11NO3
CAS-Nummer:
Molekulargewicht:
241.24
Beilstein:
225973
MDL-Nummer:
UNSPSC-Code:
12161501
PubChem Substanz-ID:
NACRES:
NA.32

Assay

≥95% (UV)

Form

solid

mp (Schmelzpunkt)

223-225 °C (lit.)

Löslichkeit

DMF: soluble
DMSO: soluble
alcohols: soluble

Fluoreszenz

λex 464 nm; λem 540 nm in methanol(lit.)
λex 571 nm; λem 585 nm in dealkylase(lit.)

Eignung

suitable for fluorescence

Lagertemp.

2-8°C

SMILES String

CCOc1ccc2N=C3C=CC(=O)C=C3Oc2c1.Fc4c(F)c(F)c(OC(=O)CNC(=O)OCC5c6ccccc6-c7ccccc57)c(F)c4F

InChI

1S/C23H14F5NO4.C14H11NO3/c24-17-18(25)20(27)22(21(28)19(17)26)33-16(30)9-29-23(31)32-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15;1-2-17-10-4-6-12-14(8-10)18-13-7-9(16)3-5-11(13)15-12/h1-8,15H,9-10H2,(H,29,31);3-8H,2H2,1H3

InChIKey

ZOSYTBPPLWBBKM-UHFFFAOYSA-N

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Anwendung

7-Ethoxyresorufin (7-ER) is a substrate used in environmental toxicology studies to monitor ethoxyresorufin-O-deethylase catalytic activity in the EROD assay. The EROD assay monitors the induction of the xenobiotic-metabolizing enzyme cytochrome P-450 (CYP) 1A1 and is a widely used biomarker for exposure of wildlife to substances that bind the aryl hydrocarbon (Ah) receptor. It provides evidence of receptor-mediated induction of cytochrome P450-dependant monooxygenases (the CYP1A subfamily specifically) by xenobiotic chemicals.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Sonstige Hinweise

Dealkylase substrate for the microfluorimetric analysis of microsomal cytochrome P-450

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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A fluorescence-microscopic method has been developed for measurement of the intracellular kinetics of the cytochrome P-450 reaction, ethoxyresorufin O-de-ethylation, in individual hepatocytes in unfixed non-frozen liver sections obtained from control or 3-methylcholanthrene-pretreated mice. De-ethylation was enhanced in the presence of

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