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Merck
모든 사진(1)

문서

96599

Sigma-Aldrich

DL-4-Hydroxy-2-ketoglutaric acid lithium salt

≥90.0% (TLC)

동의어(들):

4-Hydroxy-2-oxoglutaric acid lithium salt, DL-KHG Li

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C5H6O6 · xLi+
CAS Number:
1187-99-1
Molecular Weight:
162.10 (free acid basis)
Beilstein:
1780096
UNSPSC 코드:
12352106
NACRES:
NA.28

Quality Level

100

분석

≥90.0% (TLC)

형태

solid

불순물

≤15.0% water
3.9-8.4% lithium (anhydrous basis)

저장 온도

−20°C

InChI

1S/C5H6O6/c6-2(4(8)9)1-3(7)5(10)11/h2,6H,1H2,(H,8,9)(H,10,11)

InChI key

WXSKVKPSMAHCSG-UHFFFAOYSA-N

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생화학적/생리학적 작용

DL-4-Hydroxy-2-ketoglutaric acid (DL-KHG) is an enzyme substrate for GOT (glutamic oxalacetic aminotransferase) and 2-Keto-4-hydroxyglutarate aldolase, which catalyzes the reversible cleavage of 2-keto-4-hydroxyglutarate yielding pyruvate plus glyoxylate; DL-KHG has been used in mass spectrometry for the rapid analysis of negatively charged water-soluble cellular metabolites.

포장

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

시험 성적서(COA)

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문서 라이브러리 방문

Metabolic profiling by ion mobility mass spectrometry (IMMS).
Dwivedi, P., et al.
Metabolomics, 4, 63-80 (2008)
Enzymic synthesis of 4-methyl- and 4-ethyl-L-glutamic acids .
Echalier, F., et al.
The Journal of Organic Chemistry, 58, 2747-2750 (1993)
H C Winter et al.
Biochimica et biophysica acta, 749(1), 52-61 (1983-11-28)
Exposure of Escherichia coli 2-oxo-4-hydroxyglutarate aldolase (4-hydroxy-2-oxoglutarate glyoxylate-lyase, EC 4.1.3.16) (molecular weight = 63 000) to phosphoric acid at pH 1.6 for 10 min at 4 degrees C causes 95% or greater inactivation. No significant effect on the rate or
S C Gupta et al.
The Journal of biological chemistry, 259(16), 10012-10019 (1984-08-25)
The alpha-ketoglutarate dehydrogenase complex of either pig heart or Escherichia coli catalyzes a NAD- and CoASH-dependent oxidation of 2-keto-4-hydroxyglutarate which is stereoselective toward the L-isomer of this hydroxyketo acid. L-Malyl-CoA is the product of the reaction; the evidence includes observing
T S Taha et al.
Biochemical and biophysical research communications, 200(1), 459-466 (1994-04-15)
2-keto-3-deoxy-6-phosphogluconate aldolase (E.C. 4.1.2.14) has been purified in two chromatographic steps to 99% purity in 73% overall yield from Azotobacter vinelandii. The pure enzyme is a 70 kD trimeric Class I aldolase, inhibitable by bromopyruvate or pyruvate plus sodium borohydride
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