Phosphate → L-Leucine

Assay mixtures were prepared containing 0.613 μg LAPM, 10 μg/mL bovine serum albumin (BSA). 0.1M phosphate buffer, pH 7.2, in a total volume of 2.7 mL. Measured amounts of compounds 5 to be tested for inhibitory activity were added in additional 0.1M phosphate buffer to a total volume of 3 mL. After 72 hours at 0°-5°, 1 mL of the enzyme/inhibitor mixture was treated with 4 μL of 0.2M (L)-leucine-β-napthylamide in dimethylsulfoxide, and the rate of increase of fluorescence at 410 nm, while exciting at 310 nm. was measured. Control experiments were performed identically, except no inhibitor was present. The concentration of the selected compound 5 observed to decrease reaction rates by one-half was used to determine the value of IC50 for each compound. This was accomplished by subtracting one-half the concentration of enzyme present in the sample mixtures (1.6×10-9M) from the inhibitor concentration observed to decrease reaction rates by one-half. The results of these experiments are set forth in Table 2, above.

1. customAssay mixtures were prepared
2. additioncontaining 0.613 μg LAPM, 10 μg/mL bovine serum albumin (BSA)
3. temperaturethe rate of increase of fluorescence at 410 nm
4. customreaction rates by one-half
5. concentrationfrom the inhibitor concentration
6. customreaction rates by one-half
7. customThe results of these experiments

ORD-Eintrag

ord-0ecef83614074ff885b145a541f4f0c3

Quelldatensatz

uspto-grants-1985_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04537773