Cerotic acid
Cerotic acid structure
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Common Name | Cerotic acid | ||
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| CAS Number | 506-46-7 | Molecular Weight | 396.690 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 418.7±8.0 °C at 760 mmHg | |
| Molecular Formula | C26H52O2 | Melting Point | 86-87 °C | |
| MSDS | Chinese USA | Flash Point | 187.6±13.3 °C | |
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The uptake of trehalose glycolipids by macrophages is independent of Mincle.
ChemBioChem. 16(4) , 683-93, (2015) Trehalose glycolipids play an important role in the pathogenesis of Mycobacterium tuberculosis and are used as adjuvants for vaccines; however, much still remains unanswered about the mechanisms through which these glycolipids exert their immunomodulatory pot... |
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Development and application of a comparative fatty acid analysis method to investigate voriconazole-induced hepatotoxicity.
Clin. Chim. Acta 438 , 126-34, (2014) As fatty acids play an important role in biological regulation, the profiling of fatty acid expression has been used to discover various disease markers and to understand disease mechanisms. This study developed an effective and accurate comparative fatty aci... |
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Lipidomics reveals a remarkable diversity of lipids in human plasma.
J. Lipid Res. 51(11) , 3299-305, (2010) The focus of the present study was to define the human plasma lipidome and to establish novel analytical methodologies to quantify the large spectrum of plasma lipids. Partial lipid analysis is now a regular part of every patient's blood test and physicians r... |
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Phospholipids profiling and outcome of peritoneal dialysis patients.
Biomarkers 19(6) , 505-8, (2014) To investigate phospholipids (PLs) biomarkers in predicting outcome of patients undergoing peritoneal dialysis (PD).Twenty PD patients were followed using baseline plasma PLs with an improved online two-dimensional liquid chromatography-quadrupole time-of-fli... |
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Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice.
PLoS ONE 9(9) , e108655, (2014) The inherited peroxisomal disorder X-linked adrenoleukodystrophy (X-ALD), associated with neurodegeneration and inflammatory cerebral demyelination, is caused by mutations in the ABCD1 gene encoding the peroxisomal ATP-binding cassette (ABC) transporter ABCD1... |
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Very long chain fatty acids activate NADPH oxidase in human dermal fibroblasts.
Cell Biochem. Funct. 23(1) , 65-8, (2005) Very long chain fatty acids (VLCFAs) are exclusively oxidized in peroxisomes and their levels are significantly increased in tissues of patients with peroxisomal disorders. Although the biochemical indicators of peroxisomal dysfunction, such as elevated VLCFA... |
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Concentrations of very long-chain fatty acid in whole blood are associated with cardiovascular risk factors in children.
Clin. Chim. Acta 401(1-2) , 141-3, (2009) Fatty acid metabolism has a close relationship with metabolic syndrome. Saturated very long-chain fatty acid (hexacosanoic acid; C26:0) was recently reported to be associated with cardiovascular risk factors in adults.Eighty-eight children (47 male, 41 female... |
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Hexacosanoic and docosanoic acids plasma levels in patients with cerebral childhood and asymptomatic X-linked adrenoleukodystrophy: Lorenzo's oil effect.
Metab. Brain Dis. 23(1) , 43-9, (2008) X-linked adrenoleukodystrophy (X-ALD) is an inherited disorder of peroxisomal metabolism, biochemically characterized by deficient beta-oxidation of saturated very long chain fatty acids (VLCFA). The consequent accumulation of these fatty acids in different t... |
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High levels of saturated very long-chain fatty acid (hexacosanoic acid; C26:0) in whole blood are associated with metabolic syndrome in Japanese men.
Diabetes Res. Clin. Pract. 80(2) , 259-64, (2008) Hexacosanoic acid (C26:0) is a saturated very long-chain fatty acid and high levels of C26:0 in red blood cells are reported to be closely related with risk factors of atherosclerosis. However, the relationship between absolute levels of C26:0 in whole blood ... |
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X-linked adrenoleukodystrophy: clinical course and minimal incidence in South Brazil.
Brain Dev. 32(3) , 180-90, (2010) X-linked adenoleukodystrophy is a genetic disease that affects the degradation of very long-chain fatty acids. In male patients, common pictures are the cerebral form (CALD), myeloneuropathy (AMN), and Addison-only.To describe the clinical course of affected ... |