| Weight | 190.984 g/mol |
|---|---|
| Formula | C4H3BrN2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Bromouracil (51-20-7)
Bromouracil · Bromuracil · 5 Bromouracil
Score:
#673 in Biochemistry
,
#793 in Physics
,
#1892 in Biology
,
#2280 in Chemistry
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- Sigma-Aldrich - 5-Bromouracil18.70 - 60.30 USD
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- Partial denaturation of thymine- and 5-bromouracil-containing DNA in alkali (Journal of Molecular Biology, 1970)
- The lesions produced by ultraviolet light in DNA containing 5-bromouracil. (Quarterly Reviews of Biophysics, 1973)
- Studies on Ultraviolet Irradiation of Escherichia coli Containing 5-Bromouracil in its DNA (Microbiology, 1960)
- INDUCTION OF SPECIFIC MUTATIONS WITH 5-BROMOURACIL. (Proceedings of the National Academy of Sciences of the United States of America, 1958)
- PHOTOCHEMICAL REACTIONS OF THYMINE, URACIL, URIDINE, CYTOSINE AND BROMOURACIL IN FROZEN SOLUTION AND IN DRIED FILMS* (Photochemistry and Photobiology, 1963)
- Highly sequence-selective photoreaction of 5-bromouracil-containing deoxyhexanucleotides (Journal of the American Chemical Society, 1990)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Bromouracil
- Bromuracil
- 5 Bromouracil
-
SMILESC1=C(C(=O)NC(=O)N1)Br
-
InChIKeyLQLQRFGHAALLLE-UHFFFAOYSA-N
- Pubchem - 5-Bromouracil
- Wikipedia - bromouracil
5-Bromouracil, systematic name 5-bromopyrimidine-2,4-dione, (abbreviated as 5-BrU, 5BrUra or br5Ura) is a brominated derivative of uracil that acts as an antimetabolite or base analog, substituting for thymine in DNA, and can induce DNA mutation in the same way as 2-aminopurine. It is used mainly as an experimental mutagen, but its deoxyriboside derivative (5-bromo-2-deoxy-uridine) is used to treat neoplasms. 5-BrU exists in three tautomeric forms that have different base pairing properties.
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5-Bromouracil
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