octanoic acid has been researched along with Lipid Metabolism, Inborn Error in 10 studies
octanoic acid: RN given refers to parent cpd; structure in Merck Index, 9th ed, #1764
octanoic acid : A straight-chain saturated fatty acid that is heptane in which one of the hydrogens of a terminal methyl group has been replaced by a carboxy group. Octanoic acid is also known as caprylic acid.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (20.00) | 18.7374 |
| 1990's | 3 (30.00) | 18.2507 |
| 2000's | 2 (20.00) | 29.6817 |
| 2010's | 1 (10.00) | 24.3611 |
| 2020's | 2 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alatibi, KI | 1 |
| Tholen, S | 1 |
| Wehbe, Z | 1 |
| Hagenbuchner, J | 1 |
| Karall, D | 1 |
| Ausserlechner, MJ | 1 |
| Schilling, O | 1 |
| Grünert, SC | 1 |
| Vockley, J | 1 |
| Tucci, S | 1 |
| Nochi, Z | 1 |
| Birkler, RID | 1 |
| Fernandez-Guerra, P | 1 |
| Hansen, J | 1 |
| Wibrand, F | 1 |
| Corydon, TJ | 1 |
| Gregersen, N | 1 |
| Olsen, RKJ | 1 |
| Scaini, G | 1 |
| Simon, KR | 1 |
| Tonin, AM | 1 |
| Busanello, EN | 1 |
| Moura, AP | 1 |
| Ferreira, GC | 1 |
| Wajner, M | 2 |
| Streck, EL | 1 |
| Schuck, PF | 2 |
| Jones, PM | 1 |
| Butt, Y | 1 |
| Bennett, MJ | 1 |
| Reis de Assis, D | 1 |
| Maria, Rde C | 1 |
| Borba Rosa, R | 1 |
| Ribeiro, CA | 1 |
| da Costa Ferreira, G | 1 |
| Dutra-Filho, CS | 1 |
| Terezinha de Souza Wyse, A | 1 |
| Duval Wannmacher, CM | 1 |
| Santos Perry, ML | 1 |
| Rhead, WJ | 2 |
| Amendt, BA | 2 |
| Fritchman, KS | 1 |
| Felts, SJ | 1 |
| Wanders, RJ | 2 |
| Ijlst, L | 2 |
| van Elk, E | 1 |
| de Klerk, JB | 1 |
| Przyrembel, H | 1 |
| Demaugre, F | 1 |
| Bonnefont, JP | 1 |
| Colonna, M | 1 |
| Cepanec, C | 1 |
| Leroux, JP | 1 |
| Saudubray, JM | 1 |
10 other studies available for octanoic acid and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Lipidomic and Proteomic Alterations Induced by Even and Odd Medium-Chain Fatty Acids on Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders.
Topics: Acyl-CoA Dehydrogenase, Long-Chain; Caprylates; Cardiolipins; Cell Line; Female; Fibroblasts; Genoty | 2021 |
Increased antioxidant response in medium-chain acyl-CoA dehydrogenase deficiency: does lipoic acid have a protective role?
Topics: Acyl-CoA Dehydrogenase; Antioxidants; Caprylates; Carnitine; Cell Death; Fibroblasts; Genotype; Glyc | 2020 |
Toxicity of octanoate and decanoate in rat peripheral tissues: evidence of bioenergetic dysfunction and oxidative damage induction in liver and skeletal muscle.
Topics: Acyl-CoA Dehydrogenase; Animals; Caprylates; Creatine Kinase; Decanoates; Electron Transport; Electr | 2012 |
Accumulation of 3-hydroxy-fatty acids in the culture medium of long-chain L-3-hydroxyacyl CoA dehydrogenase (LCHAD) and mitochondrial trifunctional protein-deficient skin fibroblasts: implications for medium chain triglyceride dietary treatment of LCHAD d
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Caprylates; Cells, Cultured; Decanoates; Fibroblasts; Humans; In V | 2003 |
Inhibition of energy metabolism in cerebral cortex of young rats by the medium-chain fatty acids accumulating in MCAD deficiency.
Topics: Acetates; Acyl-CoA Dehydrogenase; Age Factors; Animals; Antifungal Agents; Antihypertensive Agents; | 2004 |
Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblasts.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Butyrates; Butyric Acid; Caprylates; Dicarboxylic A | 1983 |
Fatty acid beta-oxidation in leukocytes from control subjects and medium-chain acyl-CoA dehydrogenase deficient patients.
Topics: 3-Hydroxybutyric Acid; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Caprylates; Fatty Acids; Hum | 1992 |
Octanoate and palmitate beta-oxidation in human leukocytes: implications for the rapid diagnosis of fatty acid beta-oxidation disorders.
Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Caprylates; Fatty Acid Desaturases; Fatt | 1991 |
Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies.
Topics: Blotting, Western; Butyrates; Caprylates; Carnitine O-Palmitoyltransferase; Death, Sudden; Humans; I | 1991 |
The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Adipates; Animals; Caprylates; Electron Transport; Electro | 1986 |