| Weight | 237.984 g/mol |
|---|---|
| Formula | C4H3IN2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Iodouracil (696-07-1)
5-iodouracil, 125I-labeled · 5-iodouracil, 2-(14)C, 125I-labeled · 5-iodouracil, 123I-labeled
Score:
#1655 in Physics
,
#1877 in Biochemistry
,
#5080 in Chemistry
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- Photocrosslinking of 5-iodouracil-substituted RNA and DNA to proteins (Science, 1993)
- Cellular and molecular events leading to mitochondrial toxicity of 1-(2-deoxy-2-fluoro-1-beta-D-arabinofuranosyl)-5-iodouracil in human liver cells. (Journal of Clinical Investigation, 1995)
- Nucleic acid related compounds. 31. Smooth and efficient palladium-copper catalyzed coupling of terminal alkynes with 5-iodouracil nucleosides (Tetrahedron Letters, 1981)
- Fluorocarbohydrates in synthesis. An efficient synthesis of 1-(2-deoxy-2-fluoro-.beta.-D-arabinofuranosyl)-5-iodouracil (.beta.-FIAU) and 1-(2-deoxy-2-fluoro-.beta.-D-arabinofuranosyl)thymine (.beta.-FMAU) (Journal of Organic Chemistry, 1985)
- Imaging bacterial infections with radiolabeled 1-(2-deoxy-2-fluoro--D-arabinofuranosyl)-5-iodouracil (Proceedings of the National Academy of Sciences of the United States of America, 2005)
- Phosphorylation of the anti-hepatitis B nucleoside analog 1-(2'-deoxy-2'-fluoro-1-beta-D-arabinofuranosyl)-5-iodouracil (FIAU) by human cytosolic and mitochondrial thymidine kinase and implications for cytotoxicity. (Antimicrobial Agents and Chemotherapy, 1996)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-iodouracil, 125I-labeled
- 5-iodouracil, 2-(14)C, 125I-labeled
- 5-iodouracil, 123I-labeled
- 5-iodouracil, 131I-labeled
- 5-iodouracil, 128I-labeled
-
SMILESC1=C(C(=O)NC(=O)N1)I
-
InChIKeyKSNXJLQDQOIRIP-UHFFFAOYSA-N
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