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Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
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Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
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for maintenance.
Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
BioCyc websites down
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Metabolic Modeling Tutorial
discounted EARLY registration ends Dec 31, 2014
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Escherichia coli K-12 substr. MG1655 Compound: (1/2,5,6)-2-(3-azibutylthio)-5,6-epoxy-3-cyclohexen-1-ol

Superclasses: an organosulfur compound a thiol

Chemical Formula: C10H14N2O2S

Molecular Weight: 226.29 Daltons

Monoisotopic Molecular Weight: 226.077598394 Daltons

SMILES: CC1(N=N1)CCSC3(C(O)C2(OC2C=C3))

InChI: InChI=1S/C10H14N2O2S/c1-10(11-12-10)4-5-15-7-3-2-6-9(14-6)8(7)13/h2-3,6-9,13H,4-5H2,1H3

InChIKey: InChIKey=YQXRPUYJCCCKEH-UHFFFAOYSA-N

Unification Links: PubChem:14859132

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): 6.37

Reactions known to produce the compound:

Not in pathways:
a ubiquitin C-terminal thioester + H2O → a ubiquitin + a thiol

Enzymes inhibited by (1/2,5,6)-2-(3-azibutylthio)-5,6-epoxy-3-cyclohexen-1-ol, sorted by the type of inhibition, are:

Inhibitor (Mechanism unknown) of: lactose galactohydrolase [Helmward89]


References

Helmward89: Helmward Z "Handbook of Enzyme Inhibitors. 2nd, revised and enlarged edition." Weinheim, Federal Republic of Germany ; New York, NY, USA , 1989.


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 Mon Dec 22, 2014, biocyc11.