| Weight | 100.077 g/mol |
|---|---|
| Formula | C3H4N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
HYDANTOIN (461-72-3)
imidazolidine-2,4-dione
Score:
#2800 in Biochemistry
,
#5248 in Biology
,
#6898 in Chemistry
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- The fetal hydantoin syndrome (The Journal of Pediatrics, 1975)
- Risks to the offspring of women treated with hydantoin anticonvulsants with emphasis on the fetal hydantoin syndrome. (The Journal of Pediatrics, 1976)
- Molecular Basis of Alternating Access Membrane Transport by the Sodium-Hydantoin Transporter Mhp1 (Science, 2010)
- Prenatal Prediction of Risk of the Fetal Hydantoin Syndrome (The New England Journal of Medicine, 1990)
- THE METABOLIC CONVERSION OF 5,5-DIPHENYL HYDANTOIN TO 5-(p-HYDROXYPHENYL)-5-PHENYL HYDANTOIN (Journal of Pharmacology and Experimental Therapeutics, 1957)
- The hydantoin lesions formed from oxidation of 7,8-dihydro-8-oxoguanine are potent sources of replication errors in vivo (Biochemistry, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - imidazolidine-2,4-dione
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SMILESC1C(=O)NC(=O)N1
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InChIKeyWJRBRSLFGCUECM-UHFFFAOYSA-N
- Pubchem - HYDANTOIN
- Wikipedia - hydantoin
Hydantoin, or glycolylurea, is a heterocyclic organic compound with the formula CH2C(O)NHC(O)NH. It is a colorless solid that arises from the reaction of glycolic acid and urea. It is an oxidized derivative of imidazolidine.
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HYDANTOIN
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