ID: ALA3705371
Type: Binding
Description: In Vitro Assay: Chymase assays were performed in a total volume of 15 uL in Corning black opaque 384-well microtiter plates with a non-binding surface (Corning, N.Y.). The assay buffer was comprised of 20 mM Tris HCl pH 8.0, 50 mM NaCl, 0.01% CHAPS. The test compounds were serially diluted 3-fold with neat DMSO in a 96-well polypropylene plate from a 10 mM DMSO stock to give the 10 point dose response curve. 3 uL of the resulting DMSO solution were transferred to a 384-well polypropylene plate in duplicate, and 37 uL of assay buffer was added. Chymase was added to the assay plate in 3 uL of assay buffer followed by 2 uL of the appropriate compound dilution using a PlateMate Plus (Matrix Technologies Corp., Hudson, N.H.). The reaction was initiated by the addition of 10 uL rhodamine 110, bis-(succinoyl-L-alanyl-L-alanyl-L-prolyl-L-phenylalanylamide) (American Peptides, Sunnyvale, Calif.) in assay buffer containing 150 uM tris(2-carboxyethyl)phosphine.
Format: BAO_0000357
Organism: Homo sapiens
Target: Chymase(ALA4068)
Document: ALA3639288
BindingDB Source: 6663
Bioactivity
Activity Types for Assay ALA3705371
IC50
Parent Molecular Weight | ALogP | Polar Surface Area |
---|---|---|
347.37 | 2.56 | 2.56 |
361.40 | 2.87 | 2.87 |
344.37 | 3.23 | 3.23 |
375.43 | 3.26 | 3.26 |
420.47 | 4.81 | 4.81 |
386.45 | 4.57 | 4.57 |
423.47 | 4.15 | 4.15 |
403.48 | 4.21 | 4.21 |
437.50 | 4.46 | 4.46 |
389.46 | 3.90 | 3.90 |