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Key Documents

O9204

Sigma-Aldrich

Oxamic acid

98%

Synonym(s):

Aminooxoacetic acid, Oxalic acid monoamide

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About This Item

Linear Formula:
NH2COCO2H
CAS Number:
Molecular Weight:
89.05
Beilstein/REAXYS Number:
1743294
EC Number:
MDL number:
UNSPSC Code:
12352100

assay

98%

mp

207-210 °C (dec.) (lit.)

SMILES string

NC(=O)C(O)=O

InChI

1S/C2H3NO3/c3-1(4)2(5)6/h(H2,3,4)(H,5,6)

InChI key

SOWBFZRMHSNYGE-UHFFFAOYSA-N

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replaced by

Product No.
Description
Pricing

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Seoung-ryoung Choi et al.
Journal of medicinal chemistry, 50(16), 3841-3850 (2007-07-20)
Plasmodium falciparum lactate dehydrogenase (pfLDH) is a key enzyme for energy generation of malarial parasites and is a potential antimalarial chemotherapeutic target. It is known that the oxamate moiety, a pyruvate analog, alone shows higher inhibition against pfLDH than human
Carlotta Granchi et al.
Journal of medicinal chemistry, 54(6), 1599-1612 (2011-02-22)
Highly invasive tumor cells are characterized by a metabolic switch, known as the Warburg effect, from "normal" oxidative phosphorylation to increased glycolysis even under sufficiently oxygenated conditions. This dependence on glycolysis also confers a growth advantage to cells present in

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