| Weight | 112.092 g/mol |
|---|---|
| Formula | C3H4N4O |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Azacytosine (931-86-2)
Score:
#2620 in Biochemistry
,
#6528 in Chemistry
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- Sigma-Aldrich - 5-Azacytosine42.50 - 183.35 USD
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- Covalent bond formation between a DNA-cytosine methyltransferase and DNA containing 5-azacytosine. (Proceedings of the National Academy of Sciences of the United States of America, 1984)
- Mechanism of action of eukaryotic DNA methyltransferase: Use of 5-azacytosine-containing DNA (Journal of Molecular Biology, 1982)
- Nucleic acids components and their analogues. LI. Synthesis of 1-glycosyl derivatives of 5-azauracil and 5-azacytosine (Collection of Czechoslovak Chemical Communications, 1964)
- THE MECHANISM OF INHIBITION OF DNA (CYTOSINE-5-)-METHYLTRANSFERASES BY 5-AZACYTOSINE IS LIKELY TO INVOLVE METHYL TRANSFER TO THE INHIBITOR (Biochemical Journal, 1995)
- Mechanism of inhibition of DNA (cytosine C5)-methyltransferases by oligodeoxyribonucleotides containing 5,6-dihydro-5-azacytosine (Journal of Molecular Biology, 1999)
- p21WAF1/CIP1 induction by 5-azacytosine nucleosides requires DNA damage (Oncogene, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NC(=O)NC(=N1)N
-
InChIKeyMFEFTTYGMZOIKO-UHFFFAOYSA-N
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