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: indolepropanol phosphate

Synonyms: indole propanol phosphate, indole-3-propanol phosphate, 1-(indol-3-yl)propanol 3-phosphate, 3-(1H-indol-3-yl)propyl dihydrogen phosphate, 3-(indol-3-yl)propyl phosphate

Chemical Formula: C11H12NO4P

Molecular Weight: 253.19 Daltons

Monoisotopic Molecular Weight: 255.066044453 Daltons

SMILES: C(OP([O-])(=O)[O-])CCC1(=CNC2(=C1C=CC=C2))

InChI: InChI=1S/C11H14NO4P/c13-17(14,15)16-7-3-4-9-8-12-11-6-2-1-5-10(9)11/h1-2,5-6,8,12H,3-4,7H2,(H2,13,14,15)/p-2

InChIKey: InChIKey=NKEZSFZOUIIZFL-UHFFFAOYSA-L

Unification Links: ChEBI:231937 , PubChem:44461612

Standard Gibbs Free Energy of Change Formation (ΔfG in kcal/mol): -213.359

Enzymes inhibited by indolepropanol phosphate, sorted by the type of inhibition, are:

Inhibitor (Competitive) of: indoleglycerol phosphate aldolase [Kirschner75]

Credits:
Created 08-Feb-2010 by Fulcher C , SRI International


References

Kirschner75: Kirschner K, Wiskocil RL, Foehn M, Rezeau L (1975). "The tryptophan synthase from Escherichia coli. An improved purification procedure for the alpha-subunit and binding studies with substrate analogues." Eur J Biochem 60(2);513-23. PMID: 1107044


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 Thu Nov 27, 2014, BIOCYC13B.