Metabolic Modeling Tutorial
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Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
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Escherichia coli K-12 substr. MG1655 Compound Class: a 2-alkyl-dinitrophenol derivative

Superclasses: a nitrohydrocarbon a C-nitro compound
an aromatic compound a phenol

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


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 18.5 on Sat Nov 22, 2014, BIOCYC13A.