Compounds > 2-ethylhydracrylic acid
Page last updated: 2024-09-05

2-ethylhydracrylic acid and lactic acid

2-ethylhydracrylic acid has been researched along with lactic acid in 4 studies

Compound Research Comparison

Studies
(2-ethylhydracrylic acid)		Trials
(2-ethylhydracrylic acid)		Recent Studies (post-2010)
(2-ethylhydracrylic acid)		Studies
(lactic acid)		Trials
(lactic acid)		Recent Studies (post-2010) (lactic acid)
120346,2633,34919,053

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Green, A; Pollitt, RJ; Smith, R1
Bergh, JJ; Castagnoli, N; Mienie, LJ; Petzer, JP; Van der Schyf, CJ1
Böhmer, D; Chandoga, J; Konkoľová, J; Kováčik, J; Kramarová, V; Paučinová, I; Repiský, M1
Antonetti, G; Boenzi, S; Carrozzo, R; Catesini, G; Diodato, D; Dionisi-Vici, C; Martinelli, D; Olivieri, G; Rizzo, C; Sacchetti, E; Semeraro, M1

Other Studies

4 other study(ies) available for 2-ethylhydracrylic acid and lactic acid

ArticleYear
Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes.
    Journal of inherited metabolic disease, 1985, Volume: 8, Issue:2

    Topics: Alanine; Aldehyde Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Aminoisobutyric Acids; beta-Alanine; Child, Preschool; Humans; Hydroxybutyrates; Lactates; Lactic Acid; Male; Malonate-Semialdehyde Dehydrogenase (Acetylating); Malonates; Malondialdehyde; Methylmalonate-Semialdehyde Dehydrogenase (Acylating); Valerates

1985
Metabolic defects caused by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and by HPTP (the tetrahydropyridinyl analog of haloperidol), in rats.
    Life sciences, 2000, Apr-07, Volume: 66, Issue:20

    Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Animals; Antipsychotic Agents; Haloperidol; Lactic Acid; Male; Metabolism, Inborn Errors; Mitochondria; Oxygen Consumption; Rats; Rats, Sprague-Dawley; Valerates

2000
Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism.
    BMC medical genetics, 2017, 05-31, Volume: 18, Issue:1

    Topics: Alcohol Oxidoreductases; Aminoisobutyric Acids; DNA Mutational Analysis; Female; Gas Chromatography-Mass Spectrometry; Humans; Hydroxybutyrates; Hyperoxaluria, Primary; Infant; Lactic Acid; Urolithiasis; Valerates

2017
The urinary organic acids profile in single large-scale mitochondrial DNA deletion disorders.
    Clinica chimica acta; international journal of clinical chemistry, 2018, Volume: 481

    Topics: 3-Hydroxybutyric Acid; Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Child; Child, Preschool; Congenital Bone Marrow Failure Syndromes; DNA, Mitochondrial; Fumarates; Glutarates; Humans; Hydroxybutyrates; Infant; Kearns-Sayre Syndrome; Lactic Acid; Lipid Metabolism, Inborn Errors; Mitochondrial Diseases; Muscular Diseases; Pyruvic Acid; Retrospective Studies; Valerates

2018