Lipoxygenase Inhibitors

Application Cytochrome c has been used: in the reduction of ferricytochrome c by xanthine oxidase-generated superoxide radicals as an analyte by the single droplet deposition method using MALDI mass spectra as a terminal electron acceptor in the

Application Cytochrome c has been used: in the reduction of ferricytochrome c by xanthine oxidase-generated superoxide radicals as an analyte by the single droplet deposition method using MALDI mass spectra as a terminal electron acceptor in the

Application Cytochrome c has been used: in the reduction of ferricytochrome c by xanthine oxidase-generated superoxide radicals as an analyte by the single droplet deposition method using MALDI mass spectra as a terminal electron acceptor in the

Application Cytochrome c has been used: in the reduction of ferricytochrome c by xanthine oxidase-generated superoxide radicals as an analyte by the single droplet deposition method using MALDI mass spectra as a terminal electron acceptor in the

Application Human cytochrome P450 has been used in a study to investigate non-viral environmental risk factors for nasopharyngeal carcinoma. Human cytochrome P450 has also been used in a study to investigate the dynamics and hydration of the active

Biochem/physiol Actions Cytochrome P450 is a heterogeneous family of isozymes whose primary function is to oxidize small molecules, both as a function of intermediary metabolism (e.g.

Dabigatran ethyl ester hydrochloride is a potent inhibitor of ribosyldihydronicotinamide dehydrogenase ( NQO2 ) with an IC 50 value of 0.8 μM and a thrombin inhibitor.In VitroThe K i of dabigatran (ethyl ester hydrochloride) toward NQO2 is 0.9 μM

Dabigatran ethyl ester hydrochloride is a potent inhibitor of ribosyldihydronicotinamide dehydrogenase ( NQO2 ) with an IC 50 value of 0.8 μM and a thrombin inhibitor.In VitroThe K i of dabigatran (ethyl ester hydrochloride) toward NQO2 is 0.9 μM

Dabigatran ethyl ester hydrochloride is a potent inhibitor of ribosyldihydronicotinamide dehydrogenase ( NQO2 ) with an IC 50 value of 0.8 μM and a thrombin inhibitor.In VitroThe K i of dabigatran (ethyl ester hydrochloride) toward NQO2 is 0.9 μM

Dabigatran ethyl ester hydrochloride is a potent inhibitor of ribosyldihydronicotinamide dehydrogenase ( NQO2 ) with an IC 50 value of 0.8 μM and a thrombin inhibitor.In VitroThe K i of dabigatran (ethyl ester hydrochloride) toward NQO2 is 0.9 μM

Dabigatran ethyl ester hydrochloride is a potent inhibitor of ribosyldihydronicotinamide dehydrogenase ( NQO2 ) with an IC 50 value of 0.8 μM and a thrombin inhibitor.In VitroThe K i of dabigatran (ethyl ester hydrochloride) toward NQO2 is 0.9 μM

Mitochondrial permeability transition pore (MPTP) inhibitor. Ubiquinone analog.