HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH - Wikidata - wikimedia - TriplyDB

HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

http://www.wikidata.org/entity/Q34785768

about

Gene expression profiles of NO- and HNO-donor treated breast cancer cells: insights into tumor response and resistance pathways Fifty years of diazeniumdiolate research. From laboratory curiosity to broad-spectrum biomedical advances Aminolysis of an N-diazeniumdiolated amidine as an approach to diazeniumdiolated ammonia.Direct reaction of amides with nitric oxide to form diazeniumdiolates.Glutathione sulfinamide serves as a selective, endogenous biomarker for nitroxyl after exposure to therapeutic levels of donors.Analysis of the HNO and NO donating properties of alicyclic amine diazeniumdiolates.Soluble guanylate cyclase is required for systemic vasodilation but not positive inotropy induced by nitroxyl in the mouse.Chemotherapeutic potential of diazeniumdiolate-based aspirin prodrugs in breast cancer.Diazeniumdiolated carbamates: a novel class of nitric oxide donors Thiol Modification By Pharmacologically Active Agents of the Diazeniumdiolate Class Decoding nitric oxide release rates of amine-based diazeniumdiolates.Synthesis and chemical and biological comparison of nitroxyl- and nitric oxide-releasing diazeniumdiolate-based aspirin derivatives Enzymatic generation of the NO/HNO-releasing IPA/NO anion at controlled rates in physiological media using β-galactosidase.Stimuli-responsive polymeric nanoparticles for nanomedicine.Rapid Photoactivated Generation of Nitroxyl (HNO) under Neutral pH Conditions.HNO/cGMP-dependent antihypertrophic actions of isopropylamine-NONOate in neonatal rat cardiomyocytes: potential therapeutic advantages of HNO over NO.NO and HNO donors, nitrones, and nitroxides: Past, present, and future.Six-coordinate ferric porphyrins containing bidentate N-t-butyl-N-nitrosohydroxylaminato ligands: structure, magnetism, IR spectroelectrochemisty, and reactivity.Novel protection-deprotection strategies in diazeniumdiolate chemistry: synthesis of V-IPA/NO.

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

http://www.wikidata.org/entity/Q34785768

description

2011 nî lūn-bûn

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2011 թուականի Մարտին հրատարակուած գիտական յօդուած

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2011 թվականի մարտին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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Inorganic Chemistry

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HNO and NO release from a primary amine-based diazeniumdiolate as a function of pH

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Aloka Srinivasan

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Claudia L Torres de Holding

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Debra J Salmon

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Gens P Goodman

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Joseph E Saavedra

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Katrina M Miranda

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Keith M Davies

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Kyle V Peterson

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Larry K Keefer

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Lynta Thomas

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P2860

Nitroxyl and its anion in aqueous solutions: spin states, protic equilibria, and reactivities toward oxygen and nitric oxide

Unique oxidative mechanisms for the reactive nitrogen oxide species, nitroxyl anion.

Nitroxyl anion exerts redox-sensitive positive cardiac inotropy in vivo by calcitonin gene-related peptide signaling.

The reduction potential of nitric oxide (NO) and its importance to NO biochemistry.

Chemistry of the nitric oxide-releasing diazeniumdiolate ("nitrosohydroxylamine") functional group and its oxygen-substituted derivatives.

DNA deaminating ability and genotoxicity of nitric oxide and its progenitors.

Progress toward clinical application of the nitric oxide-releasing diazeniumdiolates.

Orthogonal properties of the redox siblings nitroxyl and nitric oxide in the cardiovascular system: a novel redox paradigm.

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 calculations

A biochemical rationale for the discrete behavior of nitroxyl and nitric oxide in the cardiovascular system.

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3262-3270

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scholarly article

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10.1021/IC101736E

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8

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50

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2011-03-15T00:00:00Z

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21405089

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