ID: ALA3705954
Type: Binding
Description: Inhibition Assay: The test substances are dissolved in 100% DMSO and serially diluted to determine their in vitro effect on PDE 9A. Typically, serial dilutions from 200 uM to 1.6 uM are prepared (resulting final concentrations in the assay: 4 uM to 0.032 uM). 2 uL portions of the diluted substance solutions are introduced into the wells of microtiter plates (Isoplate; Wallac Inc., Atlanta, Ga.). Then 50 uL of a dilution of the PDE9A preparation described above are added. The dilution of the PDE9A preparation is chosen so that less than 70% of the substrate is converted during the subsequent incubation (typical dilution: 1:10000; dilution buffer: 50 mM Tris/HCl pH 7.5, 8.3 mM MgCl2, 1.7 mM EDTA, 0.2% BSA). The substrate, [8-3H] guanosine 3'-cyclic phosphate (1 uL; Amersham Pharmacia Biotech., Piscataway, N.J.) is diluted 1:2000 with assay buffer (50 mM Tris/HCl pH 7.5, 8.3 mM MgCl2, 1.7 mM EDTA) to a concentration of 0.0005 uL.
Format: BAO_0000357
Organism: Homo sapiens
Target: Phosphodiesterase 9A(ALA3535)
Document: ALA3638367
BindingDB Source: 6465
Bioactivity
Activity Types for Assay ALA3705954
IC50
Parent Molecular Weight | ALogP | Polar Surface Area |
---|---|---|
322.41 | 3.46 | 3.46 |
363.25 | 4.15 | 4.15 |
308.39 | 3.15 | 3.15 |
338.41 | 2.51 | 2.51 |
309.37 | 2.54 | 2.54 |
356.74 | 3.50 | 3.50 |
297.36 | 2.40 | 2.40 |