| Weight | 114.104 g/mol |
|---|---|
| Formula | C4H6N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1-Methylhydantoin (616-04-6)
N-methylhydantoin
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- Purification and characterization of an ATP-dependent amidohydrolase, N-methylhydantoin amidohydrolase, from Pseudomonas putida 77. (FEBS Journal, 1995)
- The use of 13C-labelling to prove that creatinine is oxidized by mammals into creatol and 5-hydroxy-1-methylhydantoin (Journal of The Chemical Society, Chemical Communications, 1991)
- Amidohydrolysis of N-methylhydantoin coupled with ATP hydrolysis (Biochemical and Biophysical Research Communications, 1987)
- Cytosine deaminase that hydrolyzes creatinine to N-methylhydantoin in various cytosine deaminase-forming microorganisms (Archives of Microbiology, 1987)
- Excision of the oxidatively formed 5-hydroxyhydantoin and 5-hydroxy-5-methylhydantoin pyrimidine lesions by Escherichia coli and Saccharomyces cerevisiae DNA N-glycosylases. (Biochimica et Biophysica Acta, 2009)
- Creatinine and N-methylhydantoin degradation in two newly isolated Clostridium species (Archives of Microbiology, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - N-methylhydantoin
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SMILESCN1CC(=O)NC1=O
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InChIKeyRHYBFKMFHLPQPH-UHFFFAOYSA-N
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