Reaction #1620344

ord-5f7f9dc474aa498d99b67063149594d2

Reaction equation

NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](OP(=O)(O)O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
NADPH
Nc1ccccc1C(=O)C[C@H](N)C(=O)O
L-kynurenine
Nc1c(O)cccc1C(=O)C[C@H](N)C(=O)O
L-3-hydroxykynurenine

Reagents

None

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Concentrationconcentration):
  2. 2
    Concentration25 μl of different concentrations of inhibitor solutions)
  3. 3
    workup.ADDITIONThe reaction was stopped by addition of 200 μl of 1 M HClO4 after 60 min incubation

Procedure

The reaction mixture contained: 75 μl of suspended homogenate; 100 μl of substrate solution containing 50 mM K-phosphate buffer pH 7.5, 2 mM MgCl2, 0.4 mM NADPH and 50 μM L-kynurenine (final concentration): 25 μl of different concentrations of inhibitor solutions). The reaction was stopped by addition of 200 μl of 1 M HClO4 after 60 min incubation. L-3-hydroxykynurenine formed was quantified by HPLC with coulometric detection at a working voltage of +0.2 V. The column was a 10 cm C18 reversed phase (3 μm. The mobile phase consisted of 950 ml distilled water, 20 ml acetonitrile, 9 ml triethylamine, 5.9 ml phosphoric acid, 100 mg sodium EDTA and 1.5 g heptanesulfonic acid. The flow rate was 1 ml/min.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06207709B1uspto-grants-2001_03