| Weight | 140.098 g/mol |
|---|---|
| Formula | C5H4N2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
5-Formyluracil (1195-08-0)
Score:
#2384 in Biochemistry
,
#5976 in Chemistry
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- Cu(II) complexes with heterocyclic substituted thiosemicarbazones: the case of 5-formyluracil. Synthesis, characterization, x-ray structures, DNA interaction studies, and biological activity. (Inorganic Chemistry, 2003)
- Synthesis, characterisation, X-ray structure and biological activity of three new 5-formyluracil thiosemicarbazone complexes. (Journal of Inorganic Biochemistry, 2001)
- Mammalian 5-formyluracil-DNA glycosylase. 2. Role of SMUG1 uracil-DNA glycosylase in repair of 5-formyluracil and other oxidized and deaminated base lesions. (Biochemistry, 2003)
- Replication of DNA templates containing 5-formyluracil, a major oxidative lesion of thymine in DNA (Nucleic Acids Research, 1997)
- Oxidation of thymine to 5-formyluracil in DNA: mechanisms of formation, structural implications, and base excision by human cell free extracts. (Biochemistry, 1995)
- New synthetic method of 5-formyluracil-containing oligonucleotides and their melting behavior (Tetrahedron Letters, 1996)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C(=O)NC(=O)N1)C=O
-
InChIKeyOHAMXGZMZZWRCA-UHFFFAOYSA-N
- Pubchem - 5-Formyluracil
- Wikipedia - 5-formyluracil
5-Formyluracil is produced from the oxidation of the methyl group of thymine. It is mutagenic.
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5-Formyluracil
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