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Key Documents

E3763

Sigma-Aldrich

Resorufin ethyl ether

≥98% (TLC), powder

Synonym(s):

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

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1 MG
HUF 49,400.00
5 MG
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About This Item

Empirical Formula (Hill Notation):
C14H11NO3
CAS Number:
Molecular Weight:
241.24
Beilstein:
225973
MDL number:
UNSPSC Code:
12161501
PubChem Substance ID:
NACRES:
NA.47

HUF 49,400.00


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Quality Level

Assay

≥98% (TLC)

form

powder

storage condition

(Tightly closed. Dry)

technique(s)

activity assay: suitable

color

orange to red

mp

223-225 °C (lit.)

solubility

chloroform: 9.80-10.20 mg/mL, clear, orange

suitability

suitable for fluorescence

storage temp.

−20°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

InChI key

ZOSYTBPPLWBBKM-UHFFFAOYSA-N

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General description

Resorufin ethers are used as markers or substrates for different cytochrome P (CYP) isoforms. Resorufin ethyl ether is the preferred resorufin ether to be metabolized by microsomes of 3-methylcholanthrene treated animals.[1]
Resorufin is the reduced product of resazurin, also termed as Alamar Blu.[2] It exhibits fluorescence at longer wavelengths and is flexible for modification in its hydroxyl group.[3]

Research area: Cell Signaling[3]

Application

Resorufin ethyl ether is suitable for the study of dealkylating activity of cytochrome P450 isozymes 1A1 and 1A2, where arylalkyl and alkyl isothiocyanates, and their glutathione, cysteine, and A′-acetylcysteine conjugates are used as inhibitors.[4] It is suitable to study the ethoxyresorufin-O-deethylase (EROD) activity of cytochrome P450 activity (CYP1A1).[5]

Substrates

Fluorimetric substrate for cytochrome P450 linked enzyme, CXPIA1/2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Articles

Phase I biotransformation reactions increase drug compound polarity, mainly occurring in hepatic circulation.

Questions

  1. What is the solution stability of E3763?

    1 answer
    1. It is recommended to prepare solutions fresh.

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