Oxeladin citrate

a NQO1 (NAD(P)H:quinone oxidoreductase)inhibitor.

InformationIACS-010759 (IACS-10759) IACS-010759 (IACS-10759) is a potent and selective oxidative phosphorylation inhibitor (IC50 &lt: 10 nM) that blocks cellular respiration through inhibition of complex I.In vitroIACS-010759 significantly reduced

InformationIACS-010759 (IACS-10759) IACS-010759 (IACS-10759) is a potent and selective oxidative phosphorylation inhibitor (IC50 &lt: 10 nM) that blocks cellular respiration through inhibition of complex I.Targetsoxidative phosphorylation 10 nMIn

InformationIACS-010759 (IACS-10759) IACS-010759 (IACS-10759) is a potent and selective oxidative phosphorylation inhibitor (IC50 &lt: 10 nM) that blocks cellular respiration through inhibition of complex I.Targetsoxidative phosphorylation 10 nMIn

InformationIACS-010759 (IACS-10759) IACS-010759 (IACS-10759) is a potent and selective oxidative phosphorylation inhibitor (IC50 &lt: 10 nM) that blocks cellular respiration through inhibition of complex I.Targetsoxidative phosphorylation 10 nMIn

InformationIACS-010759 (IACS-10759) IACS-010759 (IACS-10759) is a potent and selective oxidative phosphorylation inhibitor (IC50 &lt: 10 nM) that blocks cellular respiration through inhibition of complex I.Targetsoxidative phosphorylation 10 nMIn

InformationIACS-010759 (IACS-10759) IACS-010759 (IACS-10759) is a potent and selective oxidative phosphorylation inhibitor (IC50 &lt: 10 nM) that blocks cellular respiration through inhibition of complex I.Targetsoxidative phosphorylation 10 nMIn

A cell-permeable &#945-cyanocinnamate compound that acts as a rapid, active site thiol modifying, time-dependent and non-competitive inhibitor of bi-directional pyruvate transport across plasma membranes in yeast, bacteria, Drosophila, and humans

General description Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic

N -( p -Amylcinnamoyl)anthranilic acid (ACA) functions as a broad spectrum phospholipase A2 inhibitor and blocks transient receptor potential (TRP) channels. It inhibits calcium activated chloride current in cardiac ventricular myocytes.

N -( p -Amylcinnamoyl)anthranilic acid (ACA) functions as a broad spectrum phospholipase A2 inhibitor and blocks transient receptor potential (TRP) channels. It inhibits calcium activated chloride current in cardiac ventricular myocytes.

N-Acetyl-L-cysteine is an acetylated amino acid with antioxidant and mucolytic properties. These two activities have made N-Acetyl-L-cysteine particularly relevant in cystic fibrosis studies, where the antioxidant/reducing character of the compound