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Escherichia coli K-12 substr. MG1655 Compound: trans-resveratrol

Synonyms: 3,4',5-trihydroxystilbene, 3,5,4'-trihydroxystilbene, 3,4',5-trihydroxy-trans-stilbene

Superclasses: a secondary metabolite a phytoalexin

Chemical Formula: C14H12O3

Molecular Weight: 228.25 Daltons

Monoisotopic Molecular Weight: 228.07864425149998 Daltons

<i>trans</i>-resveratrol compound structure

SMILES: C(=CC1(=CC(=CC(=C1)O)O))C2(C=CC(=CC=2)O)

InChI: InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+

InChIKey: InChIKey=LUKBXSAWLPMMSZ-OWOJBTEDSA-N

Unification Links: CAS:501-36-0 , ChEBI:45713 , ChemSpider:392875 , HMDB:HMDB03747 , KEGG:C03582 , KNApSAcK:C00002903 , MetaboLights:MTBLC45713 , PubChem:445154

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -39.28

Enzymes inhibited by trans-resveratrol, sorted by the type of inhibition, are:

Inhibitor (Mechanism unknown) of: ATP synthase [Dadi09]

This compound has been characterized as an alternative substrate of the following enzymes: NADPH-dependent curcumin reductase


References

Dadi09: Dadi PK, Ahmad M, Ahmad Z (2009). "Inhibition of ATPase activity of Escherichia coli ATP synthase by polyphenols." Int J Biol Macromol 45(1);72-9. PMID: 19375450


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 Sat Aug 29, 2015, biocyc14.