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Escherichia coli K-12 substr. MG1655 Compound: uridine-5'-diphosphate bromoacetol

Superclasses: an aromatic compound a bromoaromatic compound
an organic heterocyclic compound an organonitrogen heterocyclic compound a diazine a pyrimidine
an organohalogen compound an organobromine compound a bromoaromatic compound

Chemical Formula: C12H15N2O13P2Br

Molecular Weight: 537.11 Daltons

Monoisotopic Molecular Weight: 537.9389242634 Daltons

uridine-5'-diphosphate bromoacetol compound structure

SMILES: C(Br)C(=O)COP(=O)([O-])OP(=O)([O-])OCC1(OC(C(O)C(O)1)N2(C=CC(=O)NC(=O)2))

InChI: InChI=1S/C12H17BrN2O13P2/c13-3-6(16)4-25-29(21,22)28-30(23,24)26-5-7-9(18)10(19)11(27-7)15-2-1-8(17)14-12(15)20/h1-2,7,9-11,18-19H,3-5H2,(H,21,22)(H,23,24)(H,14,17,20)/p-2/t7-,9-,10-,11-/m1/s1

InChIKey: InChIKey=KUNNVLZBOWEQIC-QCNRFFRDSA-L

Unification Links: PubChem:25203077

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -639.94

Enzymes inhibited by uridine-5'-diphosphate bromoacetol, sorted by the type of inhibition, are:

Inhibitor (Mechanism unknown) of: UDP-glucose 4-epimerase [Flentke90]


References

Flentke90: Flentke GR, Frey PA (1990). "Reaction of uridine diphosphate galactose 4-epimerase with a suicide inactivator." Biochemistry 1990;29(9);2430-6. PMID: 2186813


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of EcoCyc: Nucleic Acids Research 41:D605-12 2013
Page generated by SRI International Pathway Tools version 19.0 on Wed Sep 2, 2015, biocyc12.