Quantitative production of compound I from a cytochrome P450 enzyme at low temperatures. Kinetics, activation parameters, and kinetic isotope effects for oxidation of benzyl alcohol.
about
Mechanisms of peroxynitrite interactions with heme proteinsEngineering P450 Peroxygenase to Catalyze Highly Enantioselective Epoxidation of cis-β-Methylstyrenes.Oxidation of N-Nitrosoalkylamines by human cytochrome P450 2A6: sequential oxidation to aldehydes and carboxylic acids and analysis of reaction stepsPhotooxidation of cytochrome P450-BM3.Probing 'spin-forbidden' oxygen-atom transfer: gas-phase reactions of chromium-porphyrin complexesLow temperature photo-oxidation of chloroperoxidase Compound II.Molecular probes of the mechanism of cytochrome P450. Oxygen traps a substrate radical intermediateReactive intermediates in cytochrome p450 catalysis.Kinetics and activation parameters for oxidations of styrene by Compounds I from the cytochrome P450(BM-3) (CYP102A1) heme domain and from CYP119.Cytochrome P450 119 Compounds I Formed by Chemical Oxidation and Photooxidation Are the Same Species.Beyond ferryl-mediated hydroxylation: 40 years of the rebound mechanism and C-H activation.Anilinic N-oxides support cytochrome P450-mediated N-dealkylation through hydrogen-atom transfer.Reaction Intermediates and Molecular Mechanism of Peroxynitrite Activation by NO Synthases.Oxygen Activation and Radical Transformations in Heme Proteins and Metalloporphyrins.Thiol dioxygenase turnover yields benzothiazole products from 2-mercaptoaniline and O2-dependent oxidation of primary alcohols.
P2860
Q28397657-56B0EEBF-538B-4A3C-8640-8D810C8714EEQ30276466-E0664CD5-E2D2-4819-9920-793236223612Q33707015-A05C0ECC-A3E0-4983-A973-65A755238AFAQ33718983-F5D14CD4-9B04-451B-A56D-E0F779AEE1B8Q33824607-7DC6E7E8-C095-4A57-B979-7184F5ACAD0FQ34239931-8A984044-0F1C-4F5E-94A9-881FA53FBB43Q34586651-98BFF4B3-2C82-448D-AA15-870B41048564Q34696669-863DD84A-34D4-48E0-8CE2-FFBFEA8E6BB7Q37371123-12A1800B-F76D-4C0D-9617-4F8C8E374757Q37595609-77833369-2A15-44F0-AC4C-EFF83E01C487Q37699790-AD68F04C-BBDC-4395-9128-24B8306745A6Q42021707-E05B7F5A-CC4F-4B2E-BDB9-EFAE02A73EAFQ44446386-3F549802-8550-40AC-96FC-844A2BBF9739Q47245449-6BE4580F-6669-485E-864A-06CFCD1BE625Q51824887-96E2D0BA-801C-410B-81D5-AB34BBE53F93
P2860
Quantitative production of compound I from a cytochrome P450 enzyme at low temperatures. Kinetics, activation parameters, and kinetic isotope effects for oxidation of benzyl alcohol.
description
2009 nî lūn-bûn
@nan
2009 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Quantitative production of com ...... r oxidation of benzyl alcohol.
@ast
Quantitative production of com ...... r oxidation of benzyl alcohol.
@en
type
label
Quantitative production of com ...... r oxidation of benzyl alcohol.
@ast
Quantitative production of com ...... r oxidation of benzyl alcohol.
@en
prefLabel
Quantitative production of com ...... r oxidation of benzyl alcohol.
@ast
Quantitative production of com ...... r oxidation of benzyl alcohol.
@en
P2093
P2860
P356
P1476
Quantitative production of com ...... r oxidation of benzyl alcohol.
@en
P2093
John H Horner
Martin Newcomb
P2860
P304
10629-10636
P356
10.1021/JA9031105
P407
P577
2009-08-01T00:00:00Z