| Weight | 113.076 g/mol |
|---|---|
| Formula | C3H3N3O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
6-Azauracil (461-89-2)
azauracil
Score:
#2326 in Biochemistry
,
#4629 in Biology
,
#5873 in Chemistry
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- 6-Azauracil inhibition of GTP biosynthesis in Saccharomyces cerevisiae. (Current Genetics, 1992)
- Nucleic acids components and their analogues. LI. Synthesis of 1-glycosyl derivatives of 5-azauracil and 5-azacytosine (Collection of Czechoslovak Chemical Communications, 1964)
- Inhibition of orotidylic acid decarboxylase, a primary site of carcinostasis by 6-azauracil. (Biochimica et Biophysica Acta, 1958)
- Mutations in the Second Largest Subunit of RNA Polymerase II Cause 6-Azauracil Sensitivity in Yeast and Increased Transcriptional Arrest in Vitro (Journal of Biological Chemistry, 1996)
- Mutations in the Saccharomyces cerevisiae RPB1 Gene Conferring Hypersensitivity to 6-Azauracil (Genetics, 2005)
- Structure-Function Relationship of Yeast S-II in Terms of Stimulation of RNA Polymerase II, Arrest Relief, and Suppression of 6-Azauracil Sensitivity (Journal of Biological Chemistry, 1995)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - azauracil
-
SMILESC1=NNC(=O)NC1=O
-
InChIKeySSPYSWLZOPCOLO-UHFFFAOYSA-N
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