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About This Item
Linear Formula:
NH2COCOONa
CAS Number:
Molecular Weight:
111.03
UNSPSC Code:
12352202
NACRES:
NA.77
PubChem Substance ID:
EC Number:
209-290-5
Beilstein/REAXYS Number:
6538153
MDL number:
Product Name
Sodium oxamate, ≥98%
InChI
1S/C2H3NO3.Na/c3-1(4)2(5)6;/h(H2,3,4)(H,5,6);/q;+1/p-1
InChI key
RQVZIJIQDCGIKI-UHFFFAOYSA-M
SMILES string
[Na+].NC(=O)C([O-])=O
biological source
synthetic (organic)
assay
≥98%
form
powder
mp
300 °C
solubility
water: 50 mg/mL, clear, colorless
Quality Level
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Application
Sodium oxamate has been used:
- as one of the variable in flow injection analysis
- in in vitro angiogenesis assay
- to confirm the stimulatory role of stearic acid on lactate dehydrogenase mediated lactate production
Biochem/physiol Actions
Sodium oxamate influences the fatty acid metabolism. It might be useful for the treatment of diabetes.
Structural analog of pyruvate, inhibits L(+)-lactate dehydrogenase and derails the entire gluconeogenic pathway. Binding studies with lactate dehydrogenase; Mechanism of inhibition of mitochondrial pyruvate metabolism
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Joshua Marshall Thornburg et al.
Breast cancer research : BCR, 10(5), R84-R84 (2008-10-17)
Glycolysis is increased in breast adenocarcinoma cells relative to adjacent normal cells in order to produce the ATP and anabolic precursors required for survival, growth and invasion. Glycolysis also serves as a key source of the reduced form of cytoplasmic
Role of ATP during the initiation of microvascularization: acceleration of an autocrine sensing mechanism facilitating chemotaxis by inorganic polyphosphate
Muller Werner EG, et al.
The Biochemical Journal, 475(20), 3255-3273 (2018)
Otic Antiinfectives-Advances in Research and Application, 56-56 (2013)
Huo-Lei Peng et al.
Photochemistry and photobiology, 93(5), 1193-1203 (2017-04-10)
Fluorescence of Reduced Nicotinamide Adenine Dinucleotide (NADH) is extensively employed in studies of oxidoreductases. A substantial amount of static and kinetic work has focused on the binding of pyruvate or substrate mimic oxamate to the binary complex of lactate dehydrogenase
Black Inventors: Crafting Over 200 Years of Success, 5(20), 13092-13092 (2012)
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