From 3-Methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon to 2,5,6-Trihydroxy-3-methylpyridine and 2-Oxobut-3-enanoate

Graphic of the reaction.

Medline reference

Schach S, Schwarz G, Fetzner S, Lingens F. Biol Chem Hoppe Seyler (1993) 374(3): 175-81.

Search Medline for 3-methylquinoline degradation.

3 citations on March 09, 2012.

                                 3-Methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon                                 
                                                              |
                                                              |  H2O
  3-methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon | /
                                            hydratase-adolase |/
                                                      4.2.1.- |
                                                              |
                                                       ExPASy |
                                                              |
                                                              v
                                   2,5,6-Trihydroxy-3-methylpyridine + 2-Oxobut-3-enanoate                                   

EAWAG-BBD Biotransformation rules in accord with this reaction:

3-Methyl-5-hydroxy-6-(3-carboxy-3-oxopropenyl)-1H-2-pyridon derivative -----> 2,5,6-Trihydroxy-3-methylpyridine derivative (bt0282)

Page Author(s): Sandy Etienne and David J De Grio
February 01, 2006 Contact Us

This is the EAWAG-BBD reaction, reacID# r0051.
It was generated on December 3, 2024 at 11:43:52 AM CST.

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