BDBM50294168 1-(2-(1H-indol-5-yloxy)ethyl)piperidine-4-carboxylic acid::1-[2-(1H-indol-5-yloxy)ethyl]piperidine-4-carboxylic acid::CHEMBL562164

SMILES OC(=O)C1CCN(CCOc2ccc3[nH]ccc3c2)CC1

InChI Key InChIKey=WEUOMMCSMCVWHD-UHFFFAOYSA-N

Data  2 IC50

PDB links: 1 PDB ID matches this monomer.

Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50294168   

TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
deCODE biostructures, Inc.

Curated by ChEMBL
LigandPNGBDBM50294168(1-(2-(1H-indol-5-yloxy)ethyl)piperidine-4-carboxyl...)
Show SMILES OC(=O)C1CCN(CCOc2ccc3[nH]ccc3c2)CC1
Show InChI InChI=1S/C16H20N2O3/c19-16(20)12-4-7-18(8-5-12)9-10-21-14-1-2-15-13(11-14)3-6-17-15/h1-3,6,11-12,17H,4-5,7-10H2,(H,19,20)
Affinity DataIC50: 9.66E+5nMAssay Description:Inhibition of hydrolase activity of human recombinant LTA4H expressed in Escherichia coli BL21-AI/pRARE assessed as LTB4 formation by tandem quadrupo...More data for this Ligand-Target Pair
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
deCODE biostructures, Inc.

Curated by ChEMBL
LigandPNGBDBM50294168(1-(2-(1H-indol-5-yloxy)ethyl)piperidine-4-carboxyl...)
Show SMILES OC(=O)C1CCN(CCOc2ccc3[nH]ccc3c2)CC1
Show InChI InChI=1S/C16H20N2O3/c19-16(20)12-4-7-18(8-5-12)9-10-21-14-1-2-15-13(11-14)3-6-17-15/h1-3,6,11-12,17H,4-5,7-10H2,(H,19,20)
Affinity DataIC50: 1.49E+6nMAssay Description:Inhibition of peptidase activity of human recombinant LTA4H expressed in Escherichia coli BL21-AI/pRAREMore data for this Ligand-Target Pair