Weight | 87.078 g/mol |
---|---|
Formula | C3H5NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
Glycidamide (5694-00-8)
2-oxiranecarboxamide · (+--)-oxiranecarboxamide · oxiranecarboxamide
Score:
#380 in Biochemistry
,
#1337 in Biology
,
#1556 in Chemistry
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- DNA adduct formation from acrylamide via conversion to glycidamide in adult and neonatal mice. (Chemical Research in Toxicology, 2003)
- Formation of hemoglobin adducts of acrylamide and its epoxide metabolite glycidamide in the rat (Toxicology and Applied Pharmacology, 1991)
- DNA adducts derived from administration of acrylamide and glycidamide to mice and rats (Mutation Research-genetic Toxicology and Environmental Mutagenesis, 2005)
- Acrylamide is metabolized to glycidamide in the rat: evidence from hemoglobin adduct formation (Chemical Research in Toxicology, 1990)
- Role of CYP2E1 in the Epoxidation of Acrylamide to Glycidamide and Formation of DNA and Hemoglobin Adducts (Toxicological Sciences, 2005)
- Genotoxicity of Acrylamide and Glycidamide (Journal of the National Cancer Institute, 2004)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-oxiranecarboxamide
- (+--)-oxiranecarboxamide
- oxiranecarboxamide
- oxirane-2-carboxamide
- 2,3-epoxypropanamide
- glycidic acid amide
-
SMILESC1C(O1)C(=O)N
-
InChIKeyFMAZQSYXRGRESX-UHFFFAOYSA-N
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