| Weight | 140.142 g/mol |
|---|---|
| Formula | C6H8N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
5-Ethyluracil (4212-49-1)
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- Method for treating hepatitis B virus infections using 1-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-5-ethyluracil (1991)
- 1-(2-Deoxy-2-fluoro-.beta.-D-arabinofuranosyl)-5-ethyluracil. A highly selective antiherpes simplex agent (Journal of Medicinal Chemistry, 1987)
- Synthesis and antiviral activities of arabinofuranosyl-5-ethylpyrimidine nucleosides. Selective antiherpes activity of 1-(beta-D-arabinofuranosyl)-5-ethyluracil. (Journal of Medicinal Chemistry, 1979)
- Replacement of 5-methyluracil (thymine) by 5-ethyluracil in bacterial DNA. (Biochemical and Biophysical Research Communications, 1965)
- Inhibition of Simian varicella virus infection of monkeys by 1-(2-deoxy-2-fluoro-1--d-arabinofuranosyl)-5-ethyluracil (FEAU) and synergistic effects of combination with human recombinant interferon- (Antiviral Research, 1990)
- Replacement of thymine by 5-ethyluracil in bacteriophage DNA (Biochemical and Biophysical Research Communications, 1966)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC1=CNC(=O)NC1=O
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InChIKeyRHIULBJJKFDJPR-UHFFFAOYSA-N
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Alternate Names
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Similar Compounds
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ethyl (6-oxo-1,6-dihydro-5-pyrimidinyl)acetate
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(2-amino-6-oxo-1,6-dihydro-5-pyrimidinyl)acetic acid
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24048-74-6
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(51727-06-1)
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3,6-dimethylpyrimidine-2,4(1h,3h)-dione
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4-Oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid
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6-Chloro-3-methyluracil
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5-Ethyluracil
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