| Weight | 237.0 g/mol |
|---|---|
| Formula | C4H4IN3O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Iodocytosine (1122-44-7)
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- On the temperature dependence of the two-dimensional condensation of 5-iodocytosine at the mercury/electrolyte interface (Journal of Electroanalytical Chemistry, 1982)
- Inhibition of human and woodchuck hepatitis virus DNA polymerase by the triphosphates of acyclovir, 1-(2-deoxy-2-fluoro--d-arabinofuranosyl)-5-iodocytosine and E-5-(2-bromovinyl)-2-deoxyuridine (Antiviral Research, 1984)
- Therapeutic activities of 1-(2-fluoro-2-deoxy-beta-D-arabinofuranosyl)-5-iodocytosine and -thymine alone and in combination with acyclovir and vidarabine in mice infected intracerebrally with herpes simplex virus. (Antimicrobial Agents and Chemotherapy, 1983)
- Distribution, Metabolism, and Excretion of 1-(2-Fluoro-2-deoxy--d-arabinofuranosyl)thymine and 1-(2-Fluoro-2-deoxy--d-arabinofuranosyl)-5-iodocytosine (Cancer Research, 1983)
- Infrared spectra and tautomerism of 5-fluorocytosine, 5-bromocytosine and 5-iodocytosine. Matrix isolation and theoretical AB initio studies (Journal of Molecular Structure, 1990)
- Human cytomegalovirus-induced DNA polymerase and its interaction with the triphosphates of 1-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-5-methyluracil, -5-iodocytosine, and -5-methylcytosine. (Journal of Virology, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=NC(=O)NC(=C1I)N
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InChIKeyUFVWJVAMULFOMC-UHFFFAOYSA-N
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