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Q0380

Sigma-Aldrich

Quinone Oxidoreductase 2 (NQO2) human

recombinant, expressed in E. coli, ≥90% (SDS-PAGE), ≥100 units/mg protein

Synonym(e):

NQO2 human, NRH nitroreductase human, NRH quinone reductase human

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About This Item

MDL-Nummer:
MFCD03458332
UNSPSC-Code:
12352204
NACRES:
NA.54

Rekombinant

expressed in E. coli

Qualitätsniveau

200

Assay

≥90% (SDS-PAGE)

Form

lyophilized powder (one vial contains one mg protein)

Spezifische Aktivität

≥100 units/mg protein

UniProt-Hinterlegungsnummer

P16083

Lagertemp.

−20°C

Angaben zum Gen

human ... NQO2(4835)

Anwendung

Quinone oxidoreductase 2 has been used in a study to investigate whether recent advances in limiting paraquat′s toxicity makes it safer for use as an herbicide. Quinone oxidoreductase 2 has also been used in a study to investigate the NQO2-mediated toxicity of the chemotherapeutic drug CB1954.
The product from Sigma has been used to identify novel inhibitors of the enzyme NQO2. It has also been used to investigate the effect of afobazole on quinone reductase 2 activity.

Biochem./physiol. Wirkung

Modulation of NQO2 activity can have effects on the levels and functions of the tumour suppressor, p53. Deletion of NQO2 can alter intra-cellular signalling via the NF-κB pathway.
Unique human oxidoreductase that uses Dihydronicotinamide riboside (NRH) as a cosubstrate, not NAD(P)H. Activates anticancer prodrugs. Putative melatonin receptor.

Einheitendefinition

One unit will catalyze the oxidation of one micromole of 1-methyl-1,4-dihydronicotinamide to 1-methylnicotinamide per minute in the presence of menadione at pH 7.4 at 37 °C.

Physikalische Form

contains 10% PBS buffer salts

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Effect of Afobazole on Activity of Quinone Reductase 2
Kadnikov IA, et al.
Pharmaceutical Chemistry Journal, 47(10), 514-516 (2014)
Karen A Nolan et al.
Molecular cancer therapeutics, 11(1), 194-203 (2011-11-18)
The National Cancer Institute chemical database has been screened using in silico docking to identify novel nanomolar inhibitors of NRH:quinone oxidoreductase 2 (NQO2). The inhibitors identified from the screen exhibit a diverse range of scaffolds and the structure of one
Paraquat Research. Do Recent Advances In Limiting Its Toxicity Make Its Use Safer?
Baltazar, T., et al.
British Journal of Pharmacology (2012)
K A Nolan et al.
Bioorganic & medicinal chemistry letters, 20(9), 2832-2836 (2010-04-02)
The purpose of the work was to identify novel inhibitors of the enzyme NQO2. Using computational molecular modelling, a QSAR (R(2)=0.88) was established, relating inhibitory potency with calculated binding affinity. From this, the imidazoacridin-6-one, NSC660841, was identified as the most
Faisal Hayat et al.
International journal of molecular sciences, 22(3) (2021-01-28)
As catabolites of nicotinamide possess physiological relevance, pyridones are often included in metabolomics measurements and associated with pathological outcomes in acute kidney injury (AKI). Pyridones are oxidation products of nicotinamide, its methylated form, and its ribosylated form. While they are
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