2,5-dihydroxybenzoic acid has been researched along with Alkaptonuria in 1 studies
2,5-dihydroxybenzoic acid: RN given refers to parent cpd; a oxidative product of saligenin
2,5-dihydroxybenzoic acid : A dihydroxybenzoic acid having the two hydroxy groups at the 2- and 5-positions.
Alkaptonuria: An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Gentisic acid (GA), a metabolite of acetylsalicylic acid (ASA), and homogentisic acid (HGA), which is excreted at high levels in alkaptonuria, are divalent phenolic acids with very similar structures." | 3.96 | Novel absorbance peak of gentisic acid following the oxidation reaction. ( Ejima, Y; Hirakawa, E; Hosokawa, S; Morinishi, T; Ohsaki, H; Shimosawa, T; Shukuya, K; Sogabe, K; Tokuhara, Y, 2020) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hosokawa, S | 1 |
| Shukuya, K | 1 |
| Sogabe, K | 1 |
| Ejima, Y | 1 |
| Morinishi, T | 1 |
| Hirakawa, E | 1 |
| Ohsaki, H | 1 |
| Shimosawa, T | 1 |
| Tokuhara, Y | 1 |
1 other study available for 2,5-dihydroxybenzoic acid and Alkaptonuria
| Article | Year |
|---|---|
Novel absorbance peak of gentisic acid following the oxidation reaction.
Topics: Alkaptonuria; Aspirin; Chromatography, Liquid; Gentisates; Homogentisic Acid; Humans; Mass Spectrome | 2020 |