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A highly reactive P450 model compound I
Seth R. Bell,
John Taylor Groves
Chemistry
High Meadows Environmental Institute
Princeton Materials Institute
Research output
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Contribution to journal
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Article
›
peer-review
149
Scopus citations
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Engineering & Materials Science
Acids
10%
Carboxylic acids
16%
Cytochrome P-450 Enzyme System
41%
Electrospray ionization
21%
Hydrogen
17%
Hydroxylation
60%
Isotopes
13%
Mass spectrometry
14%
Modulation
8%
Monitoring
6%
Nuclear magnetic resonance
13%
Oxidation
19%
Oxidation-Reduction
14%
Oxygen
8%
Porphyrins
39%
Positive ions
13%
Rate constants
41%
Reaction rates
12%
Substrates
7%
Xanthenes
100%
Medicine & Life Sciences
4-ethylbenzoic acid
26%
Carbon-13 Magnetic Resonance Spectroscopy
15%
Catalytic Domain
10%
Cations
11%
Cytochrome P-450 Enzyme System
21%
Electrospray Ionization Mass Spectrometry
15%
ferryl iron
19%
fluorene-4-carboxylic acid
1%
Hydrogen
12%
Hydroxylation
38%
Isotopes
12%
Kinetics
24%
meso-tetrakis(1-methyl-4-pyridiniumyl)porphyrin
28%
Oxidation-Reduction
10%
Oxygen
7%
Porphyrins
28%
Proton Magnetic Resonance Spectroscopy
13%
Xanthenes
83%
xanthydrol
24%
Chemical Compounds
13C NMR Spectroscopy
10%
4-Ethylbenzoic Acid
30%
Acid
5%
Aqueous Solution
7%
Bond Energy
16%
Cation
8%
Cleavage
10%
Cytochrome P450
31%
Electrospray Ionization Mass Spectrometry
14%
Hydrogen
7%
Kinetic Isotope Effect
16%
Oxidation Reaction
13%
Porphyrin
24%
Rate Constant
29%
Reaction Yield
6%
Redox Potential
14%
Transition State
12%
Xanthene
59%