| Weight | 89.05 g/mol |
|---|---|
| Formula | C2H3NO3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
OXAMIC ACID (66257-53-2, 471-47-6)
Oxamidic Acid · Oxalamic Acid · Aminooxoacetic Acid
Score:
#1616 in Biochemistry
,
#4624 in Chemistry
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- N-(4-substituted-thiazolyl)oxamic acid derivatives, a new series of potent, orally active antiallergy agents. (Journal of Medicinal Chemistry, 1983)
- Synthesis and structure-activity relationships of oxamic acid and acetic acid derivatives related to L-thyronine. (Journal of Medicinal Chemistry, 1995)
- The role of glycolysis in the growth of tumor cells. I. Effects of oxamic acid on the metabolism of ehrlich ascites tumor cells in vitro. (Journal of Biological Chemistry, 1961)
- The anaerobic metabolism of metronidazole forms N-(2-hydroxyethyl)-oxamic acid. (Journal of Pharmacology and Experimental Therapeutics, 1979)
- Oxamic acid derivatives for the prevention of immediate type hypersensitivity reactions (1975)
- The role of glycolysis in the growth of tumor cells. II. The effect of oxamic acid on the growth of HeLa cells in tissue culture. (Journal of Biological Chemistry, 1961)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Oxamidic Acid
- Oxalamic Acid
- Aminooxoacetic Acid
-
SMILESC(=O)(C(=O)O)N
-
InChIKeySOWBFZRMHSNYGE-UHFFFAOYSA-N
- Pubchem - OXAMIC ACID
- Wikipedia - oxamic acid
Oxamic acid is the organic compound with the formula H2NC(O)CO2H. It is a white, water-soluble solid. It is the monoamide of oxalic acid.
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acetate
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OXAMIC ACID
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