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P0928

Sigma-Aldrich

O7-Pentylresorufin

Synonym(e):

7-Pentyloxy-3H-phenoxazin-3-on, Pentoxyresorufin

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About This Item

Empirische Formel (Hill-System):
C17H17NO3
CAS-Nummer:
87687-03-4
Molekulargewicht:
283.32
Beilstein:
8394939
MDL-Nummer:
MFCD00037664
UNSPSC-Code:
12161501
PubChem Substanz-ID:
24898138
NACRES:
NA.47

Assay

≥98% (TLC)

Qualitätsniveau

200

Form

powder

Löslichkeit

acetonitrile: 0.95- 1.05 mg/mL, clear, orange

Lagertemp.

2-8°C

SMILES String

CCCCCOc1ccc2N=C3C=CC(=O)C=C3Oc2c1

InChI

1S/C17H17NO3/c1-2-3-4-9-20-13-6-8-15-17(11-13)21-16-10-12(19)5-7-14(16)18-15/h5-8,10-11H,2-4,9H2,1H3

InChIKey

ZPSOKQFFOYYPKC-UHFFFAOYSA-N

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Allgemeine Beschreibung

Resorufin pentyl ether is an analog of resazurin. Resorufin is a redox probe which is colorless and non-fluorescent in its reduced state. On oxidation, it fluoresces red. Resorufin is used widely as an indicator in microbiological media. It can be used to differentiate between actively metabolizing cells and inactive or dead cells.

Anwendung

Resorufin pentyl ether has been used as a substrate to study the effects of Kaempferia parviflora extract on mouse hepatic cytochrome P450 enzymes.

Biochem./physiol. Wirkung

Fluorimetric substrate for cytochrome P450 linked enzymes, CYP2B and CYP2B4.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
0000312734
0000185060
0000223698
0000097701
0000265592

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Canan Sapmaz et al.
Drug and chemical toxicology, 43(1), 13-21 (2018-05-19)
Morin is a flavonoid which is present in many plants. Endosulfan and 7,12-dimethylbenz[a]anthracene (DMBA) are toxic chemicals that humans are exposed to in their daily lives. In this study, the protective role of morin was investigated in endosulfan and DMBA
R B van Breemen et al.
Drug metabolism and disposition: the biological fate of chemicals, 26(2), 85-90 (1998-03-28)
An on-line mass spectrometric method has been developed to generate and identify drug metabolites formed by hepatic cytochromes P450. This method, pulsed ultrafiltration-mass spectrometry, may be used for rapid screening of drugs to determine their extent of metabolism by microsomal
Antibacterial activity of resazurin-based compounds against Neisseria gonorrhoeae in vitro and in vivo
Deanna M
International Journal of Antimicrobial Agents (2016)
Aline Y O Matsuo et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 147(1), 78-84 (2007-09-11)
Wild stocks of Pacific salmon in the Northwestern United States have declined in recent years, and the major factors contributing to these losses include water pollution and loss of habitat. In salmon, sublethal chemical exposures may impact critical behaviors (such
Jeroen Kool et al.
Drug metabolism and disposition: the biological fate of chemicals, 35(4), 640-648 (2007-01-26)
A high resolution screening (HRS) technology is described, in which gradient high-performance liquid chromatography (HPLC) is connected on-line to three parallel placed bioaffinity detection systems containing mammalian cytochromes P450 (P450s). The three so-called enzyme affinity detection (EAD) systems contained, respectively
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