Réaction #65750

ord-999afb882a784b7095001e8b321dd85f

Équation de réaction

Oc1ccc(I)cc1
p-iodophenol
O=C(O)CN(CCN(CC(=O)O)CC(=O)O)CC(=O)O
EDTA
OO
H2O2
OO
H2O2
c1cnc2ccnnc2c1
pyridopyridazine
Nc1cccc2c(=O)[nH][nH]c(=O)c12
luminol

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONby mixing
  2. 2
    workup.ADDITIONcontaining horseradish peroxidase at the concentrations of 10 pg/ml, 100 pg/ml 1 ng/ml or 10 ng/ml
  3. 3
    Autreof the tubes, chemiluminescent reaction

Mode opératoire

The pyridopyridazine compound (L-012) as obtained in Example 3 and luminol were dissolved at the concentration of 0.2 mM in 0.2 M Tris buffer (pH 8.6) containing 0.1 mM EDTA. In test tubes were put 990 μl respectively of the solutions, and to each of the solutions was added 10 μl of a dimethylsulfoxide (DMSO) solution of 40 mM p-iodophenol as a chemiluminescent enhancer, followed by mixing. In other test tubes were put 50 μl of each of the mixtures, whereto 100 μl of a 0.2 M Tris buffer (pH 8.6) containing horseradish peroxidase at the concentrations of 10 pg/ml, 100 pg/ml 1 ng/ml or 10 ng/ml. By further adding 50 μl of Tris buffer (pH 8.6) containing of 0.6 mM H2O2 to each of the tubes, chemiluminescent reaction was initiated. The measurement was carried out for the luminous amounts for 10 seconds between 60 seconds later and 70 seconds later after addition of H2O2. The results are tabulated in Table 3. From Table 3, it was shown that the pyridopyridazine compound of Example 3 (L-012) provides about 4 to 20 times as great chemiluminescent amounts as luminol. The sodium salt of L-012 showed the same chemiluminescence activity as L-012.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05420275uspto-grants-1995_05