Potent methyl oxidation of 5-methyl-2'-deoxycytidine by halogenated quinoid carcinogens and hydrogen peroxide via a metal-independent mechanism.
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An Exceptionally Facile Two-Step Structural Isomerization and Detoxication via a Water-Assisted Double Lossen RearrangementWhy Does 2,3,5,6-Tetrachlorophenol Generate the Strongest Intrinsic Chemiluminescence among All Nineteen Chlorophenolic Persistent Organic Pollutants during Environmentally-friendly Advanced Oxidation Process?Mechanism of Intrinsic Chemiluminescence Production from the Degradation of Persistent Chlorinated Phenols by the Fenton System: A Structure-Activity Relationship Study and the Critical Role of Quinoid and Semiquinone Radical Intermediates.A combined experimental and computational investigation on the unusual molecular mechanism of the Lossen rearrangement reaction activated by carcinogenic halogenated quinonesDeamination features of 5-hydroxymethylcytosine, a radical and enzymatic DNA oxidation product.Fingerprinting DNA Oxidation Processes: IR Characterization of the 5-Methyl-2′-Deoxycytidine Radical Cation
P2860
Potent methyl oxidation of 5-methyl-2'-deoxycytidine by halogenated quinoid carcinogens and hydrogen peroxide via a metal-independent mechanism.
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2013 nî lūn-bûn
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
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name
Potent methyl oxidation of 5-m ...... a metal-independent mechanism.
@ast
Potent methyl oxidation of 5-m ...... a metal-independent mechanism.
@en
type
label
Potent methyl oxidation of 5-m ...... a metal-independent mechanism.
@ast
Potent methyl oxidation of 5-m ...... a metal-independent mechanism.
@en
prefLabel
Potent methyl oxidation of 5-m ...... a metal-independent mechanism.
@ast
Potent methyl oxidation of 5-m ...... a metal-independent mechanism.
@en
P2093
P2860
P1476
Potent methyl oxidation of 5-m ...... a metal-independent mechanism.
@en
P2093
Balaraman Kalyanaraman
Ben-Zhan Zhu
Chun-Hua Huang
P2860
P304
P356
10.1016/J.FREERADBIOMED.2013.01.010
P577
2013-01-30T00:00:00Z