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39953
Lauroyl-L-carnitin
≥95.0% (HPLC)
Synonym(e):
(2R)-3-Carboxy-N,N,N-trimethyl-2-[(1-oxododecyl)-oxy]-1-propanaminium Inneres Salz, L-Carnitin-dodecanoylester, C12-Carnitine, Dodecanoyl-L-carnitin
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| Packungsgröße | SKU | Verfügbarkeit | Preis |
|---|---|---|---|
| 10 mg | Warenkorb auf Verfügbarkeit prüfen | CHF 120.00 | |
| 50 mg | Warenkorb auf Verfügbarkeit prüfen | CHF 490.00 |
Über diesen Artikel
Empirische Formel (Hill-System):
C19H37NO4
CAS-Nummer:
Molekulargewicht:
343.50
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.26
Beilstein/REAXYS Number:
4147610
Technischer Dienst
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Unterstützung erhaltenQuality Level
assay
≥95.0% (HPLC)
form
powder or crystals
optical activity
[α]/D -20±2°, c = 1 in methanol
packaging
pkg of 10 mg, pkg of 50 mg
impurities
≤10% water
color
white to off-white
functional group
ester
storage temp.
2-8°C
SMILES string
C[N+](C)(C)C[C@H](OC(CCCCCCCCCCC)=O)CC([O-])=O
InChI
1S/C19H37NO4/c1-5-6-7-8-9-10-11-12-13-14-19(23)24-17(15-18(21)22)16-20(2,3)4/h17H,5-16H2,1-4H3/t17-/m1/s1
InChI key
FUJLYHJROOYKRA-QGZVFWFLSA-N
General description
Lauroyl-L-carnitine, or Dodecanoylcarnitine, is an acylcarnitine compound with essential roles in energy metabolism. Synthesized in the liver from methionine, this metabolite of lysine is integral in various metabolic processes, making it a valuable asset in both biochemical and metabolomics research. Its concentration can serve as a diagnostic marker, particularly in cases of carnitine deficiency, and is of significance in assessing disease activity and diagnosing conditions like HIV and chronic hepatitis B infections. Additionally, Lauroyl-L-carnitine is associated with fatty acid oxidation disorders, including long-chain acyl CoA dehydrogenase deficiency and carnitine palmitoyltransferase I/II deficiency, further enhancing its relevance in metabolic research and diagnosis[1]. This acylcarnitine compound has also been detected in cancer tissues, human serum, and tissue biopsies, expanding its applications and potential contributions to various areas of metabolomics research.
Application
Lauroyl-L-carnitine finds application in biochemical research and metabolomics research.
Biochem/physiol Actions
Lauroyl-L-carnitine is an acylcarnitine is present in fatty acid oxidation disorders such as long-chain acyl CoA dehydrogenase deficiency, carnitine palmitoyltransferase I deficiency, and carnitine palmitoyltransferase II deficiency.
Features and Benefits
- Can be used in Metabolomics and Biochemical research
- High-quality compound suitable for multiple research applications
Other Notes
For additional information on our range of Biochemicals, please complete this form.
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Dieser Artikel | |||
|---|---|---|---|
| functional group ester | functional group ester | functional group - | functional group - |
| assay ≥95.0% (HPLC) | assay ≥94.0% (HPLC) | assay ≥94.0% (HPLC) | assay ≥97.0% (HPLC) |
| packaging pkg of 10 mg, pkg of 50 mg | packaging - | packaging - | packaging - |
| form powder or crystals | form powder or crystals | form powder or crystals | form powder |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. 2-8°C | storage temp. 2-8°C |
| color white to off-white | color - | color white to off-white | color white |
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Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Yosuke Shigematsu et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 792(1), 63-72 (2003-06-28)
In a selective screening for fatty acid oxidation disorders by tandem mass spectrometry, we tested the diagnostic ratios and acylcarnitine concentrations in sera or blood spots, which were reported to be specific to very long-chain acyl CoA dehydrogenase deficiency, carnitine
R J Morrow et al.
Clinica chimica acta; international journal of clinical chemistry, 211(1-2), 73-81 (1992-10-15)
Carnitine esters from acetylcarnitine (C2 acyl chain) to octadecanoylcarnitine (C18 acyl chain) can be extracted from urine with recoveries of greater than 80%. However, to obtain such recoveries, it is important to choose the method of extraction appropriate to the
Grzegorz Godlewski et al.
Cell metabolism, 29(6), 1320-1333 (2019-05-21)
Endocannabinoids acting on the cannabinoid-1 receptor (CB1R) or ghrelin acting on its receptor (GHS-R1A) both promote alcohol-seeking behavior, but an interaction between the two signaling systems has not been explored. Here, we report that the peripheral CB1R inverse agonist JD5037
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 39953-50MG | 04061833238769 |
| 39953-10MG | 04061833238752 |