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Raczyńska, Ewa D.; Hallmann, Małgorzata; Duczmal, Kinga (March 2011). "Quantum-chemical studies of amide–iminol tautomerism for inhibitor of lactate dehydrogenase: Oxamic acid".
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Zarzyka-Niemiec, Iwona (2008-10-05). "Hydroxyalkylation of oxamic acid with propylene carbonate: Synthesis, composition, and properties of products".
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Except where otherwise noted, data are given for materials in their
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Miskimins WK, Ahn HJ, Kim JY, Ryu S, Jung YS, Choi JY (2014).
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548:"Synergistic anti-cancer effect of phenformin and oxamate"
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400:complex, effectively inhibiting it.
431:, the conjugate base of oxamic acid
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38:Ball and stick model of oxamic acid
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380:. Oxamic acid inhibits
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390:lactate dehydrogenase
63:Amino(oxo)acetic acid
50:Preferred IUPAC name
327:Solubility in water
302: g·mol
69:Aminooxoacetic acid
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310:White solid
81:Identifiers
67:2-oxoglycine
61:Other names
17:Oxamic acid
386:active site
378:oxalic acid
358:Oxamic acid
307:Appearance
270:Properties
160:100.006.768
54:Oxamic acid
725:Categories
532:2016-12-14
436:References
295:Molar mass
206:QU60N5OPLG
133:ChemSpider
109:3D model (
88:CAS Number
654:0021-8995
619:2210-271X
413:polyester
584:24465604
552:PLOS ONE
526:Archived
423:See also
370:C(O)COOH
332:Soluble
287:C(O)COOH
98:471-47-6
575:3897486
522:PubChem
429:Oxamate
417:epoxide
405:polymer
320:209 °C
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173:PubChem
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384:. The
360:is an
300:89.050
254:SMILES
44:Names
676:This
374:amide
111:JSmol
682:stub
650:ISSN
615:ISSN
580:PMID
498:ISBN
469:ISBN
398:NADH
197:UNII
642:doi
638:110
607:doi
603:964
570:PMC
560:doi
461:doi
394:LDH
388:of
376:of
223:EPA
186:974
176:CID
142:949
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