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3-hydroxyanthranilic acid and Mitochondrial Diseases

3-hydroxyanthranilic acid has been researched along with Mitochondrial Diseases in 1 studies

3-Hydroxyanthranilic Acid: An oxidation product of tryptophan metabolism. It may be a free radical scavenger and a carcinogen.
3-hydroxyanthranilic acid : An aminobenzoic acid that is benzoic acid substituted at C-2 by an amine group and at C-3 by a hydroxy group. It is an intermediate in the metabolism of the amino acid tryptophan.
3-hydroxyanthranilate : A hydroxybenzoate that is the conjugate base of 3-hydroxyanthranilic acid.

Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Reyes-Ocampo, J1
Ramírez-Ortega, D1
Cervantes, GI1
Pineda, B1
Balderas, PM1
González-Esquivel, D1
Sánchez-Chapul, L1
Lugo-Huitrón, R1
Silva-Adaya, D1
Ríos, C1
Jiménez-Anguiano, A1
Pérez-de la Cruz, V1

Other Studies

1 other study available for 3-hydroxyanthranilic acid and Mitochondrial Diseases

ArticleYear
Mitochondrial dysfunction related to cell damage induced by 3-hydroxykynurenine and 3-hydroxyanthranilic acid: Non-dependent-effect of early reactive oxygen species production.
    Neurotoxicology, 2015, Volume: 50

    Topics: 3-Hydroxyanthranilic Acid; Animals; Astrocytes; Brain; Cells, Cultured; Cerebral Cortex; Disease Mod

2015