Pathway Tools
Intro Tutorial
discounted registration ends Sept 5, 2015
Pathway Tools
Intro Tutorial
discounted registration ends Sept 5, 2015
Pathway Tools
Intro Tutorial
discounted registration ends Sept 5, 2015
Pathway Tools
Intro Tutorial
discounted registration ends Sept 5, 2015
Pathway Tools
Intro Tutorial
discounted registration ends Sept 5, 2015
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

(1/2,5,6)-2-(3-azibutylthio)-5,6-epoxy-3-cyclohexen-1-ol compound structure

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

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 19.0 on Fri Aug 28, 2015, BIOCYC14B.