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Escherichia coli K-12 substr. MG1655 Compound Class: a 2-alkyl-dinitrophenol derivative

Superclasses: a nitrohydrocarbona C-nitro compound
an aromatic compounda phenol

a 2-alkyl-dinitrophenol derivative compound structure

SMILES: C([R1])C1(=C(O)C([N+](=O)[O-])=CC([N+](=O)[O-])=C1)

Reactions known to produce the compound:

Not in pathways:
a phenol sulfate + H2O → a phenol + sulfate + H+

Enzymes inhibited by a 2-alkyl-dinitrophenol derivative, sorted by the type of inhibition, are:

Inhibitor (Competitive) of: fumarate reductase [Comment 1], succinate:quinone oxidoreductase Inhibitor (Noncompetitive) of: fumarate reductase [Maklashina99, Comment 2]

References

Maklashina99: Maklashina E, Cecchini G (1999). "Comparison of catalytic activity and inhibitors of quinone reactions of succinate dehydrogenase (Succinate-ubiquinone oxidoreductase) and fumarate reductase (Menaquinol-fumarate oxidoreductase) from Escherichia coli." Arch Biochem Biophys 1999;369(2);223-32. PMID: 10486141


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Please cite the following article in publications resulting from the use of EcoCyc: Nucleic Acids Research 41:D605-12 2013
Page generated by Pathway Tools version 19.5 (software by SRI International) on Thu Feb 11, 2016, biocyc13.