O-octanoylcarnitine

O-octanoylcarnitine is a lipid of Fatty Acyls (FA) class.

Cross Reference

There are no associated biomedical information in the current reference collection.

Current reference collection contains 212 references associated with O-octanoylcarnitine in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

Users can download the reference list at the bottom of this page and read the reference manually to find out biomedical information.


Here are additional resources we collected from PubChem and MeSH for O-octanoylcarnitine

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with O-octanoylcarnitine

MeSH term MeSH ID Detail
Starvation D013217 47 associated lipids
Ventricular Dysfunction, Left D018487 33 associated lipids
Heart Failure, Systolic D054143 3 associated lipids
Total 3

NCBI Entrez Crosslinks

All references with O-octanoylcarnitine

Download all related citations
Per page 10 20 50 100 | Total 64
Authors Title Published Journal PubMed Link
Ojuka E et al. Measurement of β-oxidation capacity of biological samples by respirometry: a review of principles and substrates. 2016 Am. J. Physiol. Endocrinol. Metab. pmid:26908505
Horscroft JA et al. Altered Oxygen Utilisation in Rat Left Ventricle and Soleus after 14 Days, but Not 2 Days, of Environmental Hypoxia. 2015 PLoS ONE pmid:26390043
Kim M et al. Association between arterial stiffness and serum L-octanoylcarnitine and lactosylceramide in overweight middle-aged subjects: 3-year follow-up study. 2015 PLoS ONE pmid:25781947
Donato AJ et al. The impact of ageing on adipose structure, function and vasculature in the B6D2F1 mouse: evidence of significant multisystem dysfunction. 2014 J. Physiol. (Lond.) pmid:25038241
Stride N et al. Decreased mitochondrial oxidative phosphorylation capacity in the human heart with left ventricular systolic dysfunction. 2013 Eur. J. Heart Fail. pmid:23115323
Meadows JA and Wargo MJ Characterization of Pseudomonas aeruginosa growth on O-acylcarnitines and identification of a short-chain acylcarnitine hydrolase. 2013 Appl. Environ. Microbiol. pmid:23524670
Naccarato A et al. Identification and assay of underivatized urinary acylcarnitines by paper spray tandem mass spectrometry. 2013 Anal Bioanal Chem pmid:23907684
Morand R et al. Quantification of plasma carnitine and acylcarnitines by high-performance liquid chromatography-tandem mass spectrometry using online solid-phase extraction. 2013 Anal Bioanal Chem pmid:23995505
Alexandre-Gouabau MC et al. Maternal and cord blood LC-HRMS metabolomics reveal alterations in energy and polyamine metabolism, and oxidative stress in very-low birth weight infants. 2013 J. Proteome Res. pmid:23527880
Tonin AM et al. Disruption of redox homeostasis in cerebral cortex of developing rats by acylcarnitines accumulating in medium-chain acyl-CoA dehydrogenase deficiency. 2012 Int. J. Dev. Neurosci. pmid:22472139
Larsen S et al. Increased mitochondrial substrate sensitivity in skeletal muscle of patients with type 2 diabetes. 2011 Diabetologia pmid:21424396
Schönfeld P et al. Mitochondrial fatty acid oxidation and oxidative stress: lack of reverse electron transfer-associated production of reactive oxygen species. 2010 Jun-Jul Biochim. Biophys. Acta pmid:20085746
Smith EH et al. Allelic diversity in MCAD deficiency: the biochemical classification of 54 variants identified during 5 years of ACADM sequencing. 2010 Mol. Genet. Metab. pmid:20434380
Khalid JM et al. Relationship of octanoylcarnitine concentrations to age at sampling in unaffected newborns screened for medium-chain acyl-CoA dehydrogenase deficiency. 2010 Clin. Chem. pmid:20413428
De Jesús VR et al. Comparison of amino acids and acylcarnitines assay methods used in newborn screening assays by tandem mass spectrometry. 2010 Clin. Chim. Acta pmid:20122909
Arnold GL et al. Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State. 2010 Mol. Genet. Metab. pmid:20036593
Kraunsøe R et al. Mitochondrial respiration in subcutaneous and visceral adipose tissue from patients with morbid obesity. 2010 J. Physiol. (Lond.) pmid:20421291
Tsuchida H et al. Identification of a novel organic anion transporter mediating carnitine transport in mouse liver and kidney. 2010 Cell. Physiol. Biochem. pmid:20332632
Maier EM et al. Dissection of biochemical borderline phenotypes in carriers and genetic variants of medium-chain acyl-CoA dehyrogenase deficiency: implications for newborn screening [corrected]. 2009 Clin. Genet. pmid:19780764
Hsu HW et al. Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening. 2008 Pediatrics pmid:18450854