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Merck

73097

L-Argininosuccinic acid lithium salt

≥95% (TLC)

Synonim(y):

N-{{[(4S)-4-Amino-4-carboxybutyl]amino}iminomethyl}-L-aspartic acid lithium salt, Lithium L-argininosuccinate

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Wybierz wielkość

10 MG

775,00 zł

50 MG

3160,00 zł

775,00 zł


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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C10H18N4O6 · xLi+
Masa cząsteczkowa:
290.27 (free acid basis)
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
Beilstein/REAXYS Number:
6933810

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InChI

1S/C10H18N4O6.Li/c11-5(8(17)18)2-1-3-13-10(12)14-6(9(19)20)4-7(15)16;/h5-6H,1-4,11H2,(H,15,16)(H,17,18)(H,19,20)(H3,12,13,14);/q;+1/t5-,6-;/m0./s1

SMILES string

OC(C[C@@H](C(O)=O)NC(NCCC[C@H](N)C(O)=O)=N)=O.[Li+]

InChI key

MGJRREWOOITZBB-GEMLJDPKSA-N

assay

≥70% (qNMR), ≥95% (TLC)

form

powder or crystals

optical activity

[α]/D 15±2°, c = 1 in H2O

impurities

≤20% water

color

white to off-white

storage temp.

2-8°C

Quality Level

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Ta pozycja
72715L225072764
form

powder or crystals

form

solid

form

powder

form

powder or crystals

assay

≥70% (qNMR), ≥95% (TLC)

assay

≥98.0% (TLC)

assay

≥98% (titration)

assay

≥95.0% (HPLC)

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

impurities

≤20% water

impurities

≤10% water

impurities

<2% water (Karl Fischer)

impurities

-

color

white to off-white

color

white to off-white

color

white

color

-

Biochem/physiol Actions

Arginosuccinic acid is a basic amino acid, which is synthesized by some cells from citrulline, aspartic acid and used as a precursor for arginine in the urea cycle or Citrulline-NO cycle. The reaction is catalyzed by the enzyme argininosuccinate synthetase. Argininosuccinic acid is a precursor to fumarate in the citric acid cycle via argininosuccinate lyase. Defects in the arginosuccinate lyase enzyme can lead to arginosuccinate lyase deficiency. Argininosuccinate (ASA) lyase deficiency results in defective cleavage of ASA. This leads to an accumulation of ASA in cells and an excessive excretion of ASA in urine (arginosuccinic aciduria). In virtually all respects, this disorder shares the characteristics of other urea cycle defects. The most important characteristic of ASA lyase deficiency is its propensity to cause hyperammonemia in affected individuals. ASA in affected individuals is excreted by the kidney at a rate practically equivalent to the glomerular filtration rate (GFR). Whether ASA itself causes a degree of toxicity due to hepatocellular accumulation is unknown; such an effect could help explain hyperammonemia development in affected individuals. Regardless, the name of the disease is derived from the rapid clearance of ASA in urine, although elevated levels of ASA can be found in plasma. ASA lyase deficiency is associated with high mortality and morbidity rates.
Metabolite in alanine, aspartate, glutamate, arginine, and proline metabolic pathways, and in the biosynthesis of secondary metabolites and amino acids.
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Klasa składowania

11 - Combustible Solids

wgk

WGK 3


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Wing Lok Au et al.
Journal of the neurological sciences, 209(1-2), 101-104 (2003-04-11)
A 25-year-old Chinese man presented with a 2-year history of recurrent coma. His plasma ammonia level was extremely elevated, with raised citrulline level and absence of argininosuccinic acid. Adult-onset citrullinaemia, a condition rarely reported outside the Japanese population, was diagnosed.
L D Fleisher et al.
American journal of human genetics, 31(4), 439-445 (1979-07-01)
We have monitored two successive pregnancies in a family which we found to be at risk for argininosuccinic aciduria. We measured argininosuccinic acid (ASA) concentrations in amniotic fluid and utilized an indirect assay of ASA lyase activity in cultured amniotic
Pornswan Wasant et al.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 85 Suppl 2, S720-S731 (2002-10-31)
Urea Cycle Disorders (UCD) is an inborn error of urea synthesis in which ammonium and other nitrogenous precursors of urea accumulate leading to episodic coma and a high mortality rate. Therapy with peritoneal dialysis, essential amino acids or their nitrogen-free
W J Kleijer et al.
Journal of inherited metabolic disease, 25(5), 399-410 (2002-11-01)
A biochemical variant of argininosuccinate lyase deficiency, found in five individuals, is introduced. In comparison to classical patients, the variant cases of argininosuccinate lyase deficiency were characterized by residual enzyme activity as measured by the incorporation of [14C]citrulline into proteins.
Rachel S Carling et al.
Clinical chemistry and laboratory medicine, 58(5), 758-768 (2019-10-18)
Background Quantification of plasma amino acids is key to the diagnosis of inherited defects of amino acid synthesis, catabolism and transport, many of which present as clinical emergencies. The utility of this test is limited by the long analysis time

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