about
Photoinduced release of nitroxyl and nitric oxide from diazeniumdiolatesNitroxyl (HNO) reacts with molecular oxygen and forms peroxynitrite at physiological pH. Biological Implications.The chemistry of nitroxyl-releasing compounds.Mechanism of pH-dependent decomposition of monoalkylamine diazeniumdiolates to form HNO and NO, deduced from the model compound methylamine diazeniumdiolate, density functional theory, and CBS-QB3 calculationsNitrosyl hydride (HNO) replaces dioxygen in nitroxygenase activity of manganese quercetin dioxygenaseThe chemistry and biology of nitroxyl (HNO): a chemically unique species with novel and important biological activity.Biological signaling by small inorganic moleculesThe pharmacology of nitroxyl (HNO) and its therapeutic potential: not just the Janus face of NOSynthesis and characterization of lithium oxonitrate (LiNO).Nitrosyl hydride (HNO) as an O2 analogue: long-lived HNO adducts of ferrous globins.The emergence of nitroxyl (HNO) as a pharmacological agent.Six-coordinate ferric porphyrins containing bidentate N-t-butyl-N-nitrosohydroxylaminato ligands: structure, magnetism, IR spectroelectrochemisty, and reactivity.DFT study of the mechanism of manganese quercetin 2,3-dioxygenase: quest for origins of enzyme unique nitroxygenase activity and regioselectivity.Reactions of Hydrated Singly Charged First-Row Transition-Metal Ions M+(H2O)n(M=V, Cr, Mn, Fe, Co, Ni, Cu, and Zn) toward Nitric Oxide in the Gas Phase
P2860
Q33284032-C113237B-CC5E-4A13-BA80-060A8952ADA9Q34738088-3A829232-3E5E-43F3-B91D-9F3674DCD216Q35040403-8D7D0C3C-DD91-4B97-BFC1-F6EC34B83C69Q35187446-EF3EDEB9-DE30-4EEB-817E-DCC43F6231E3Q35571299-56929EE5-5661-4AF7-B010-A253BE8D22F9Q35993929-E9E27F15-1E20-4108-BE80-36EF47225268Q36376440-0A96C1AD-D853-4D3D-8659-D4C2B7E70D36Q36408421-A46507A1-32A9-43DB-B8AC-B356C28FB511Q36457239-C2CB1795-B485-4243-A25C-1FD45373D68BQ37370685-5DADE90F-0C20-4730-B707-53101C4548E3Q37385327-AE573A9D-3200-442F-AFD0-272C755B1AF9Q50780501-FBAF6F42-582E-401C-95A2-BDBC7AB99293Q52870034-22F67688-9360-43C2-9D35-89857DE233C1Q59031482-5DEA9F60-27E8-4308-B761-5A5C64144873
P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
name
Spin-forbidden deprotonation of aqueous nitroxyl (HNO).
@ast
Spin-forbidden deprotonation of aqueous nitroxyl (HNO).
@en
type
label
Spin-forbidden deprotonation of aqueous nitroxyl (HNO).
@ast
Spin-forbidden deprotonation of aqueous nitroxyl (HNO).
@en
prefLabel
Spin-forbidden deprotonation of aqueous nitroxyl (HNO).
@ast
Spin-forbidden deprotonation of aqueous nitroxyl (HNO).
@en
P356
P1476
Spin-forbidden deprotonation of aqueous nitroxyl (HNO).
@en
P2093
Sergei V Lymar
Vladimir Shafirovich
P304
P356
10.1021/JA034378J
P407
P577
2003-05-01T00:00:00Z