ChemicalBook--->CAS DataBase List--->2364-67-2

2364-67-2

2364-67-2 Structure

2364-67-2 Structure
IdentificationBack Directory
[Name]

PALMITOYL CARNITINE
[CAS]

2364-67-2
[Synonyms]

C02990
Palmitylcarnitine
Palmityl-L-carnitine
L-Palmitoylcarnitine
Hexadecanoylcarnitine
Palmitoyl L-carnitine
O-palmitoyl-L-carnitine
Palmitoyl-L-Carnitine solution
Palmitoyl-L-carnitine >=97.0% (TLC)
(3R)-3-hexadecanoyloxy-4-trimethylazaniumylbutanoate
(-)-[(R)-3-Carboxylato-2-(palmitoyloxy)propyl]trimethylaminium
(2R)-3-Carboxylato-N,N,N-trimethyl-2-[(1-oxohexadecyl)oxy]-1-propanaminium
1-PropanaMiniuM, 3-carboxy-N,N,N-triMethyl-2-[(1-oxohexadecyl)oxy]-, inner salt, (2R)-
[Molecular Formula]

C23H45NO4
[MDL Number]

MFCD00152152
[MOL File]

2364-67-2.mol
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[optical activity]

[α]/D -17±2°, c = 1 in methanol
[BRN ]

4152034
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS06,GHS08
[Signal word ]

Danger
[Hazard statements ]

H225-H301+H311+H331-H370
[Precautionary statements ]

P210-P280-P301+P310+P330-P302+P352+P312-P304+P340+P311
Hazard InformationBack Directory
[Uses]

L-?Palmitoyl Carnitine is used as a diagnostic agent in the investigation of drug toxicity with respect to the liver. Acts as a biomarker in the study of metabolism in metabolic diseases.
[Definition]

ChEBI: An O-acyl-L-carnitine in which the acyl group is specified as palmitoyl (hexadecanoyl).
[General Description]

Palmitoyl-L-carnitine (PLC) belongs to the class of long chain acylcarnitine compounds. It is an acyl-chain ester, which can be obtained from L-carnitine via acylcarnitine family transferase. PLC is reported to be used for the phospholipid reacylation in erythrocyte membrane ghosts.
[Biochem/physiol Actions]

L-Palmitoylcarnitine can change the activity of several enzymes and transporters, localized in the membrane and facilitates the transfer of long-chain fatty acids from cytoplasm into mitochondria during the oxidation of fatty acids. L-Palmitoylcarnitine accumulates in ischemic myocardium and potentially contribute to myocardial damage through alterations in membrane molecular dynamics.
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