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
twitter

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 Wed Nov 26, 2014, biocyc13.