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  • Discovery of GSK2795039, a Novel Small Molecule NADPH Oxidase 2 Inhibitor.

Discovery of GSK2795039, a Novel Small Molecule NADPH Oxidase 2 Inhibitor.

Antioxidants & redox signaling (2015-07-03)
Kazufumi Hirano, Woei Shin Chen, Adeline L W Chueng, Angela A Dunne, Tamara Seredenina, Aleksandra Filippova, Sumitra Ramachandran, Angela Bridges, Laiq Chaudry, Gary Pettman, Craig Allan, Sarah Duncan, Kiew Ching Lee, Jean Lim, May Thu Ma, Agnes B Ong, Nicole Y Ye, Shabina Nasir, Sri Mulyanidewi, Chiu Cheong Aw, Pamela P Oon, Shihua Liao, Dizheng Li, Douglas G Johns, Neil D Miller, Ceri H Davies, Edward R Browne, Yasuji Matsuoka, Deborah W Chen, Vincent Jaquet, A Richard Rutter
ABSTRACT

The NADPH oxidase (NOX) family of enzymes catalyzes the formation of reactive oxygen species (ROS). NOX enzymes not only have a key role in a variety of physiological processes but also contribute to oxidative stress in certain disease states. To date, while numerous small molecule inhibitors have been reported (in particular for NOX2), none have demonstrated inhibitory activity in vivo. As such, there is a need for the identification of improved NOX inhibitors to enable further evaluation of the biological functions of NOX enzymes in vivo as well as the therapeutic potential of NOX inhibition. In this study, both the in vitro and in vivo pharmacological profiles of GSK2795039, a novel NOX2 inhibitor, were characterized in comparison with other published NOX inhibitors. GSK2795039 inhibited both the formation of ROS and the utilization of the enzyme substrates, NADPH and oxygen, in a variety of semirecombinant cell-free and cell-based NOX2 assays. It inhibited NOX2 in an NADPH competitive manner and was selective over other NOX isoforms, xanthine oxidase, and endothelial nitric oxide synthase enzymes. Following systemic administration in mice, GSK2795039 abolished the production of ROS by activated NOX2 enzyme in a paw inflammation model. Furthermore, GSK2795039 showed activity in a murine model of acute pancreatitis, reducing the levels of serum amylase triggered by systemic injection of cerulein. GSK2795039 is a novel NOX2 inhibitor that is the first small molecule to demonstrate inhibition of the NOX2 enzyme in vivo.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Phorbol 12-myristate 13-acetate, synthetic, ≥98.0% (TLC)
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HEPES, BioUltra, for molecular biology, ≥99.5% (T)
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Tetracycline, 98.0-102.0% (HPLC)
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Ethylene glycol-bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid, ≥97.0%
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Ethylene glycol-bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid, for molecular biology, ≥97.0%
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PMA, for use in molecular biology applications, ≥99% (HPLC)
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Ethylene glycol-bis(2-aminoethylether)-N,N,N′,N′-tetraacetic acid, BioXtra, ≥97 .0%
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Hypoxanthine, powder, BioReagent, suitable for cell culture
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HEPES, BioXtra, pH 5.0-6.5 (1 M in H2O), ≥99.5% (titration)
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HEPES, BioXtra, suitable for mouse embryo cell culture, ≥99.5% (titration)
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Tetracycline, 98.0-102.0% (HPLC)
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HEPES, BioPerformance Certified, ≥99.5% (titration), suitable for cell culture
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HEPES, ≥99.5% (titration)
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Dulbecco′s Modified Eagle′s Medium - high glucose, With 4500 mg/L glucose and L-glutamine, without sodium bicarbonate, powder, suitable for cell culture
Sigma-Aldrich
Hypoxanthine, ≥99.0%
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Phorbol 12-myristate 13-acetate, ≥99% (TLC), film or powder
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HEPES, anhydrous, free-flowing, Redi-Dri, ≥99.5%
Sigma-Aldrich
HEPES buffer solution, 1 M in H2O
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Xanthine, ≥99%
Sigma-Aldrich
Xanthine, BioUltra, ≥99%
Sigma-Aldrich
Xanthine, ≥99.5% (HPLC), purified by recrystallization