BDBM350527 N-(4-bromophenyl)-2-(2,4-dioxo-1,3- diazaspiro[4.5]dec-3-yl)acetamide::US10208071, Table 3.3::US10434112, Table 3.3::US10799518, Structure TABLE 3.3
SMILES Brc1ccc(NC(=O)CN2C(=O)NC3(CCCCC3)C2=O)cc1
InChI Key InChIKey=UUIRITXPYAOMCC-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 350527
Affinity DataEC50: 7.38E+5nMAssay Description:HEK-Gα16 cells stably expressing the human FPR2 receptor was utilized. Cells were plated into 384-well poly-D-lysine coated plates at a density ...More data for this Ligand-Target Pair
Affinity DataEC50: 738nMAssay Description:HEK-Gα16 cells stably expressing the human FPR2 receptor was utilized. Cells were plated into 384-well poly-D-lysine coated plates at a density ...More data for this Ligand-Target Pair
Affinity DataEC50: 738nMAssay Description:HEK-Gα16 cells stably expressing the human FPR2 receptor was utilized. Cells were plated into 384-well poly-D-lysine coated plates at a density ...More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Suez Canal University
Curated by ChEMBL
Suez Canal University
Curated by ChEMBL
Affinity DataIC50: 720nMAssay Description:Inhibition of ALR2 (unknown origin) using sodium dl-glyceraldehyde as substrate preincubated for 10 mins followed by substrate addition by UV-spectro...More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
Suez Canal University
Curated by ChEMBL
Suez Canal University
Curated by ChEMBL
Affinity DataIC50: 3.12E+4nMAssay Description:Inhibition of ALR1 (unknown origin) using sodium d-glucoronate as substrate preincubated for 10 mins followed by substrate addition by UV-spectrophot...More data for this Ligand-Target Pair