5-Bromouracil

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5-Bromouracil

IUPAC name	5-Bromo-1H-pyrimidine-2,4-dione
Other names	5-Bromo-2,4-dihydroxypyrimidine
Identifiers
Abbreviations	5-BrU 5-BU
CAS number	[51-20-7]
PubChem	5802
SMILES	C1=C(C(=O)NC(=O)N1)Br
Properties
Molecular formula	C₄H₃BrN₂O₂
Molar mass	190.983 g/mol
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references

5-Bromouracil (or 5-bromo-2,4(1H,3H)-pyrimidinedione or 5-BrU or 5-BU) 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. Its structure can also be found in 5-bromo-2-deoxy-uridine.

5-BrU exists in three tautomeric forms that have different base pairing properties. The keto form (pictured) is complementary to adenine so this can be incorporated into DNA by aligning opposite adenine residues during DNA replication. Alternatively, the enol and ion forms are complementary to guanine. This means that 5-BrU can be present in DNA either opposite adenine or guanine.

The three forms frequently interchange so base-pairing properties can become altered at any time. The result of this is that during a subsequent round of replication a different base is aligned opposite the 5-BrU residue. Further rounds of replication 'fix' the change by incorporating a normal nitrogen base into the complementary strand.

Thus 5-BrU induces a point mutation via base substitution. This base pair will change from an A-T to a G-C or from a G-C to an A-T after a number of replication cycles, depending on whether 5-BU is within the DNA molecule or is an incoming base when it is enolized or ionized.