A1509
Acetyl-DL-carnitine hydrochloride
>98% (TLC)
别名:
(±)-3-Acetoxy-4-(trimethylammonio)butyrate hydrochloride
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关于此项目
经验公式（希尔记法）:
C9H17NO4 · HCl
化学文摘社编号:
分子量:
239.70
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
219-709-3
MDL number:
产品名称
Acetyl-DL-carnitine hydrochloride,
assay
>98% (TLC)
Quality Level
form
powder
color
white
storage temp.
−20°C
SMILES string
Cl.CC(=O)OC(CC(O)=O)C[N](C)(C)C
InChI
1S/C9H18NO4.ClH/c1-7(11)14-8(5-9(12)13)6-10(2,3)4;/h8H,5-6H2,1-4H3,(H,12,13);1H
InChI key
KEOLEGXENCLAMX-UHFFFAOYSA-N
Biochem/physiol Actions
Weak cholinergic receptor agonist; intermediate in lipid metabolism.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
A S Alhomida et al.
Biochimie, 78(3), 204-208 (1996-01-01)
The kinetic properties of carnitine acetyltransferase from the skeletal muscle of the Arabian camel (Camelus dromedarius) were studied. The enzyme showed an optimum pH between 7.2 and 8.2. Reciprocal plots of data obtained by varying one substrate concentration while keeping
P D Prasad et al.
Biochimica et biophysica acta, 1284(1), 109-117 (1996-10-02)
The JAR human placental choriocarcinoma cells were found to transport carnitine into the intracellular space by a Na(+)-dependent process. The transport showed no requirement for anions. The Na+-dependent process was saturable and the apparent Michaelis-Menten constant for carnitine was 12.3
J M Mauro et al.
The Biochemical journal, 237(2), 533-540 (1986-07-15)
A photolabile reagent, p-azidophenacyl-DL-thiocarnitine, was synthesized and tested as a photoaffinity label for carnitine acetyltransferase (EC 2.3.1.7) from pigeon breast. p-Azidophenacyl-DL-thiocarnitine is an active-site-directed reagent for this acetyltransferase, since it is a competitive inhibitor (Ki 10 microM) versus carnitine. U.v.
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| A1509-1G | 04061826055144 |
| A1509-250MG | 04061832414690 |