Weight | 128.087 g/mol |
---|---|
Formula | C4H4N2O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
Isobarbituric acid (20636-41-3)
5-hydroxyuracil · 5-hydroxy-2,4(1H,3H)-pyrimidinedione · 20636-41-3
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- Major oxidative products of cytosine, 5-hydroxycytosine and 5-hydroxyuracil, exhibit sequence context-dependent mispairing in vitro. (Nucleic Acids Research, 1994)
- Structural characterization of viral ortholog of human DNA glycosylase NEIL1 bound to thymine glycol or 5-hydroxyuracil-containing DNA. (Journal of Biological Chemistry, 2012)
- Palladium Catalyzed Coupling of 5-Hydroxyuracil Trifluoromethanesulfonates (Triflates) with Alkenes and Alkynes (Heterocycles, 1987)
- NEIL1 is the major DNA glycosylase that processes 5-hydroxyuracil in the proximity of a DNA single-strand break. (Biochemistry, 2007)
- Synthesis and Cleavage of Oligodeoxynucleotides Containing a 5-Hydroxyuracil Residue at a Defined Site (Chemical Research in Toxicology, 1997)
- Base-promoted reaction of 5-hydroxyuracil derivatives with peroxyl radicals. (Organic Letters, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-hydroxyuracil
- 5-hydroxy-2,4(1H,3H)-pyrimidinedione
- 20636-41-3
-
SMILESC1=C(C(=O)NC(=O)N1)O
-
InChIKeyOFJNVANOCZHTMW-UHFFFAOYSA-N
- Pubchem - Isobarbituric acid
- Wikipedia - 5-hydroxyuracil
5-Hydroxyuracil is an oxidized form of cytosine that is produced by the oxidative deamination of cytosines by reactive oxygen species. It does not distort the DNA molecule and is bypassed by replicative DNA polymerases. It can miscode for adenine and is potentially mutagenic.
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Alternate Names
Estimated Properties
Boiling Point | 266.03 C | EPA T.E.S.T. |
---|---|---|
Boiling Point | 418.18 C | EPI Suite |
Density | 1.55 g/cm3 | EPA T.E.S.T. |
Flash Point | 199.93 C | EPA T.E.S.T. |
Melting Point | 174.38 C | EPI Suite |
Water Solubility | 10930.4 mg/L | EPA T.E.S.T. |
Water Solubility | 21193 mg/L | EPI Suite |
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