Target intelligence / Profile preview

Peroxynitrite and nitrogen dioxide radical (null)

Target
null
Molecular classification
Other (Reactive nitrogen species, Free radical, Inorganic reactive species)
01

Overview

Peroxynitrite (ONOO⁻) is a highly reactive, short-lived nitrogen species formed from the diffusion-controlled reaction of superoxide (O₂•⁻) and nitric oxide (•NO) in biological systems[1][3][7][9]. In aqueous solution, peroxynitrite exists in equilibrium with its weak acid (ONOOH, pKₐ ~6.8), decays rapidly, and is a potent oxidant and nitrating agent capable of modifying proteins, lipids, and nucleic acids—either directly or by generating secondary radicals like nitrogen dioxide (•NO₂) and hydroxyl radical (•OH)[1][3][4][5]. Nitrogen dioxide radical (•NO₂) is a major secondary product of peroxynitrite decomposition, itself a strong one-electron oxidant with selectivity for aromatic amino acids (notably causing tyrosine nitration), promoting protein and lipid damage and impacting cell signaling[1][3][4][6]. Both are not classical drug targets but are "reactive species" central to processes of oxidative/nitrosative stress, inflammation, neurodegeneration, cardiovascular pathology, and cancer where their toxic signatures (like nitrotyrosine) serve as biomarkers of tissue injury[1][3][4][9]. If you are building a structured database, these species should not be included as canonical targets, but as toxic products or contributors to disease mechanisms. Their inclusion as 'targets' is nonstandard and unorthodox, explaining the above attributes.

Other names
Peroxynitrite (ONOO⁻, peroxynitrite anion, peroxynitrous acid/ONOOH)Nitrogen dioxide radical (•NO₂, nitrogen dioxide, NO₂•)
02

Mechanism of action

Scavenging or decomposition of peroxynitrite (removal of reactive species, reduction in oxidative/nitrosative stress) Inhibition of formation (reducing superoxide or nitric oxide availability)

03

Biological functions

Oxidative stress inductionNitration and oxidation of proteins, lipids, and DNARegulation of cell signaling via oxidative modificationCell injury and cytotoxicity
04

Disease associations

InflammationNeurodegenerative diseaseCardiovascular diseaseCancerOther (broadly toxic in multiple pathological contexts)
05

Safety considerations

High toxicity and non-selectivity: Both species are extremely reactive, can damage a wide variety of biological macromolecules, and are implicated in cellular injuryAttempts to scavenge these species systemically can risk interference with physiological roles of nitric oxide and compromise normal cellular redox signaling
06

Interacting drugs

Antioxidants (e.g., uric acid, ascorbate, glutathione modulators, N-acetylcysteine)

2 more in the full profile.

07

Biomarkers

3-nitrotyrosine (formed from protein tyrosine nitration)Nitrotyrosine-modified proteinsOxidized/lipid peroxidation products

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