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Bromodeoxyuridine A nucleoside that substitutes for thymidine in DNA and thus acts as an antimetabolite. It causes breaks in chromosomes and has been proposed as an antiviral and antineoplastic agent. It has been given orphan drug status for use in the treatment of primary brain tumors.
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pre_formula( "InChI=1/C9H11BrN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)/t5-,6+,7+/m0/s1/f/h11H", "jqp065/6035.html" ); ?>
Molecular Formula:
C9H11BrN2O5
InChI: InChI=1/C9H11BrN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)/t5-,6+,7+/m0/s1/f/h11H
InChIKey: InChIKey=WOVKYSAHUYNSMH-HOWZBOOODN
SMILES: C1C(C(OC1N2C=C(C(=O)NC2=O)Br)CO)O
Names:
Bromodeoxyuridine
Bromoouridine
Broxuridine [INN]
Broxuridine
Brudr
BUDR
Radibud
5-Bromodeoxyuridine
5-Bromodesoxyuridine
5-bromo-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
5-Budr
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Registries:
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PubChem CID 6035
PubChem ID 148898
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