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cinnabarinic acid

Known as: 2-amino-3H-phenoxazin-one-1,9-dicarboxylic acid 
National Institutes of Health

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1 relation

Broader (1)

Oxazines

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Synthesis of cinnabarinic acid by metabolically engineered Pseudomonas chlororaphis GP72
Cinnabarinic acid is a valuable phenoxazinone that has broad applications in the pharmaceutical, chemical, and dyeing industries… 
2015
2015
Aryl Hydrocarbon Receptor–Dependent Stanniocalcin 2 Induction by Cinnabarinic Acid Provides Cytoprotection against Endoplasmic Reticulum and Oxidative Stress
The aryl hydrocarbon receptor (AhR) is a cytosolic ligand-activated transcription factor historically known for its role in… 
Highly Cited
2012
Highly Cited
2012
Cinnabarinic Acid, an Endogenous Metabolite of the Kynurenine Pathway, Activates Type 4 Metabotropic Glutamate Receptors
Cinnabarinic acid is an endogenous metabolite of the kynurenine pathway that meets the structural requirements to interact with… 
2008
2008
Cinnabarinic acid generated from 3‐hydroxyanthranilic acid strongly induces apoptosis in thymocytes through the generation of reactive oxygen species and the induction of caspase
3‐Hydroxyanthranilic acid (3HAA) is one of the tryptophan metabolites along the kynurenine pathway and induces apoptosis in T… 
1999
1999
3-Hydroxyanthranilic acid-derived compounds formed through electrochemical oxidation.
  • Hideo Iwahashi
  • Journal of Chromatography B: Biomedical Sciences…
  • 1999
  • Corpus ID: 44577857
Highly Cited
1995
Highly Cited
1995
Laccase‐mediated formation of the phenoxazinone derivative, cinnabarinic acid
1992
1992
Oxidation of 3-hydroxyanthranilic acid to the phenoxazinone cinnabarinic acid by peroxyl radicals and by compound I of peroxidases or catalase.
Since 3-hydroxyanthranilic acid (3HAA), an oxidation product of tryptophan metabolism, is a powerful radical scavenger [Christen… 
1990
1990
Mechanism of reaction of 3-hydroxyanthranilic acid with molecular oxygen.
Highly Cited
1987
Highly Cited
1987
Oxidative reactivity of the tryptophan metabolites 3-hydroxyanthranilate, cinnabarinate, quinolinate and picolinate.
1983
1983
Cinnabarinic acid formation in Malpighian tubules of the silkworm, Bombyx mori. Participation of catalase in cinnabarinic acid formation in the presence of manganese ion.
Cinnabarinic acid was formed from 3-hydroxyanthranilic acid during incubation with a soluble fraction from Malpighian tubules of… 
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