ライフサイエンスコーパス: diphenyliodonium

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1 nced by the inhibition of these effects with diphenyliodonium.

2 vessels and could be inhibited with SOD and diphenyliodonium.

3 by nitroblue tetrazolium, ferricyanide, and diphenyliodonium.

4 of nitroblue tetrazolium, ferricyanide, and diphenyliodonium.

5 teine but not by the NADPH oxidase inhibitor diphenyliodonium.

6 seven thiophenes with benzyne generated from diphenyliodonium-2-carboxylate (DPIC) under a standard s

7 nic F127) and the photoacid generator (PAG), diphenyliodonium-2-carboxylate monohydrate.

8 peroxidase and was inhibited by catalase or diphenyliodonium (a flavoenzyme inhibitor), similar to t

9 ROS generation was markedly inhibited by diphenyliodonium, a flavoprotein inhibitor, and by the s

10 Moreover, diphenyliodonium, a specific Nox inhibitor, blocked prol

11 Inhibition of NADPH oxidase with diphenyliodonium abolished the inhibitory effect of AngI

12 Catalase, diphenyliodonium (an inhibitor of flavoenzymes), and sur

13 er ascorbate and the NADPH oxidase inhibitor diphenyliodonium and analysis of Ca(2+) wave propagation

14 aling, including NAD(P)H oxidase inhibitors (diphenyliodonium and apocynin) or enhancement of peroxid

15 ary artery NADH oxidoreductase (1 micromol/L diphenyliodonium) and electron acceptors for NADH oxidor

16 Whereas diphenyliodonium chloride inhibited O-2, blockers of hem

17 The reaction of diphenyliodonium chloride with free reduced flavins has

18 ssed >90% by pan-flavoenzyme inhibition with diphenyliodonium chloride.

19 h readout by a photostimulated reaction with diphenyliodonium chloride.

20 Diphenyliodonium (DPI) is known to irreversibly inactiva

21 In this study, diphenyliodonium (DPI) is used as an inhibitor of flavop

22 trast, inhibition of NADPH oxidase either by diphenyliodonium (DPI) or by genetically deleting gp91(p

23 Diphenyliodonium (DPI), an inhibitor of flavoprotein-con

24 Inactivation of flavoprotein enzymes by diphenyliodonium has also been studied, and several exam

25 ion can also be triggered in the presence of diphenyliodonium nitrate (DPIN) as a photoacid under UV

26 ns of three different nucleophiles employing diphenyliodonium tosylate.

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