Weight | 112.088 g/mol |
---|---|
Formula | C4H4N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
4,6-DIHYDROXYPYRIMIDINE (1193-24-4)
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- 4-(1'-D-RIBITYLAMINO)-5-AMINO-2,6-DIHYDROXYPYRIMIDINE, THE SECOND PRODUCT OF THE RIBOFLAVIN SYNTHETASE REACTION. (Journal of Biological Chemistry, 1964)
- Active site inhibitors of HCV NS5B polymerase. The development and pharmacophore of 2-thienyl-5,6-dihydroxypyrimidine-4-carboxylic acid. (Bioorganic & Medicinal Chemistry Letters, 2004)
- Inhibition of the Synthesis of Deoxyribonucleic Acid in Bacteria by 6-(p-Hydroxyphenylazo)-2,4-dihydroxypyrimidine I. METABOLIC STUDIES IN STREPTOCOCCUS FECALIS (Journal of Biological Chemistry, 1966)
- Tautomerism of 4-Hydroxy- and 4,6-Dihydroxypyrimidine (Journal of Organic Chemistry, 1966)
- Simple pyrimidines. VII. The fine structure of 4,6-dihydroxypyrimidine (Australian Journal of Chemistry, 1964)
- 2-Substituted-4,5-dihydroxypyrimidine-6-carboxamide antiviral targeted libraries. (ACS Combinatorial Science, 2009)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(N=CNC1=O)O
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InChIKeyDUFGYCAXVIUXIP-UHFFFAOYSA-N
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