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
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
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MetaCyc Compound: dinitrophenylhydrazine

Synonyms: 2,4-dinitrophebylhydrazine, 1-hydrazine-2,4-dinitrobenzene, 2,4-dnph, hydrazine, (2,4-dinitrophenyl)-

Superclasses: a nitrohydrocarbon a C-nitro compound

Chemical Formula: C6H6N4O4

Molecular Weight: 198.14 Daltons

Monoisotopic Molecular Weight: 200.054554766 Daltons

SMILES: C1(C=C(NN)C(=CC=1[N+]([O-])=O)[N+](=O)[O-])

InChI: InChI=1S/C6H6N4O4/c7-8-5-2-1-4(9(11)12)3-6(5)10(13)14/h1-3,8H,7H2

InChIKey: InChIKey=HORQAOAYAYGIBM-UHFFFAOYSA-N

Unification Links: ChEBI:66932 , ChemSpider:15468522 , KEGG:C11283 , PubChem:3772977

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -21.393278 Inferred by computational analysis [Latendresse13]

Enzymes inhibited by dinitrophenylhydrazine, sorted by the type of inhibition, are:

Inhibitor (Competitive) of: factor-independent urate hydroxylase [Bachrach57]


References

Bachrach57: Bachrach, U (1957). "The aerobic breakdown of uric acid by certain pseudomonads." J Gen Microbiol 17(1);1-11. PMID: 13475666

Latendresse13: Latendresse M. (2013). "Computing Gibbs Free Energy of Compounds and Reactions in MetaCyc."


Report Errors or Provide Feedback
Please cite the following article in publications resulting from the use of MetaCyc: Caspi et al, Nucleic Acids Research 42:D459-D471 2014
Page generated by SRI International Pathway Tools version 18.5 on Mon Nov 24, 2014, BIOCYC13B.