| Weight | 127.103 g/mol |
|---|---|
| Formula | C4H5N3O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
6-Azathymine (932-53-6)
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- TCI - 6-Azathymine45.00 USD
- Photosensitized cycloadditions to 1,3-dimethyl-6-azauracil and 1,3-dimethyl-6-azathymine. An imine linkage unusually reactive toward photocycloaddition. (Journal of the American Chemical Society, 1974)
- Studies on the mechanism of action of 6-azathymine. I. Biosynthesis of the deoxyriboside. (Journal of Biological Chemistry, 1955)
- Effect of the deoxyriboside of 6-azathymine (azathymidine) on the biosynthesis of deoxyribonucleic acid by bone marrow and neoplastic cells (in vitro). (Biochimica et Biophysica Acta, 1956)
- Synthesis and biological evaluation of l- and d-configuration 1,3-dioxolane 5-azacytosine and 6-azathymine nucleosides (Bioorganic & Medicinal Chemistry Letters, 2000)
- Nucleic acid components and their analogues. IX. N-Methyl derivatives of 6-azauracil and 6-azathymine (Collection of Czechoslovak Chemical Communications, 1961)
- Decrease of sensitivity to ultraviolet radiation of Streptococcus faecalis grown in media supplemented with 6-azathymine, an analog of thymine. (Biochimica et Biophysica Acta, 1962)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=NNC(=O)NC1=O
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InChIKeyXZWMZFQOHTWGQE-UHFFFAOYSA-N
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6-Azathymine
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