4-Aryl-1,3,2-oxathiazolylium-5-olates as pH-controlled NO-donors: The next generation of S-nitrosothiols

Medicine & Life Sciences

• S-Nitrosothiols 100%
• Nitric Oxide Donors 76%
• Nitric Oxide 51%
• Spin Trapping 32%
• Electron Spin Resonance Spectroscopy 27%
• N-methyl-D-glucamine dithiocarbamate 21%
• 5,5-dimethyl-1-pyrroline-1-oxide 18%
• Density Functional Theory 18%
• Electrons 16%
• Spectrophotometry 13%
• Vasodilation 10%
• Glutathione 9%
• Acids 7%

Chemical Compounds

• Nitric Oxide Donor 88%
• Nitric Oxide 60%
• Spin Trapping 37%
• EPR Spectroscopy 27%
• Ascorbate 17%
• N-Oxide 16%
• DFT-B3LYP Calculation 16%
• Acidic Condition 15%
• Glutathione 14%
• Spectrophotometry 14%
• Ring Opening Reaction 13%
• Electron Spin 13%
• Substitution Reaction 9%
• UV/VIS Spectroscopy 9%
• Density Functional Theory 9%
• Reduction 7%
• pH Value 6%
• Application 4%

Engineering & Materials Science

• Nitric oxide 86%
• Paramagnetic resonance 28%
• Biological systems 24%
• Electrons 21%
• Glutathione 19%
• Vasodilation 18%
• Spectrophotometry 16%
• Density functional theory 15%
• Pulse code modulation 12%
• Substitution reactions 10%
• Acids 9%
• Iron 9%
• Oxides 9%
• Derivatives 8%
• Decomposition 7%