< Back to small molecule database

BDBM50188027

E3L047856
Internal ID: BDB047856
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB047856/BDB047856.sdf
Basic Properties
Compound ID
E3L047856
Internal ID
BDB047856
Molecular formula
C26H28N2O4
Molecular weight
432.520000
Exact mass
432.204907
XLogP
5.2697
TPSA
77.4900
HBA / HBD
4 / 1
Rotatable bonds
10
Heavy atoms / rings
32 / 4
Activity summary
EC50 unknown 90.00000000 nM
4 activity record(s) imported
InChIKey
DKDATBYVPQYIRT-UHFFFAOYSA-N
SMILES
CCOC(Cc1cccc2c1ccn2CCCc1nc(-c2ccccc2)oc1C)C(=O)O
Aliases
BDBM50188027 (preferred) 2-ethoxy-3-(1-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)-1H-indol-4-yl)propanoic acid (source_name) BDBM50188027 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
P37231 PPARG;NR1C3
Peroxisome proliferator-activated receptor gamma
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50188027 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50188027 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50188027 Open - 10.1016/j.bmcl.2006.05.007 PMID: 16737814
PubChem CID10455509 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCOC(Cc1cccc2c1ccn2CCCc1nc(-c2ccccc2)oc1C)C(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB047856/BDB047856.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB047856/BDB047856.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB047856/BDB047856.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB047856/BDB047856.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB047856/BDB047856.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50188027 IC50 756 nM Moderate DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50188027 EC50 190 nM Moderate DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50188027 IC50 274 nM Moderate DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50188027 EC50 90 nM High DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1