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BDBM50188029

E3L047858
Internal ID: BDB047858
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB047858/BDB047858.sdf
Basic Properties
Compound ID
E3L047858
Internal ID
BDB047858
Molecular formula
C24H23ClN2O4
Molecular weight
438.911000
Exact mass
438.134635
XLogP
5.3386
TPSA
77.4900
HBA / HBD
4 / 1
Rotatable bonds
8
Heavy atoms / rings
31 / 4
Activity summary
IC50 unknown 73.00000000 nM
4 activity record(s) imported
InChIKey
PAWOPJKHTZCKMT-QFIPXVFZSA-N
SMILES
CCO[C@@H](Cc1ccc2c(ccn2Cc2nc(-c3ccccc3Cl)oc2C)c1)C(=O)O
Aliases
BDBM50188029 (preferred) (2S)-3-(1-{[2-(2-chlorophenyl)-5-methyl-1,3-oxazol-4-yl]methyl}-1H-indol-5-yl)-2-ethoxypropanoic acid (source_name) BDBM50188029 (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:BDBM50188029 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50188029 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50188029 Open - 10.1016/j.bmcl.2006.05.007 PMID: 16737814
PubChem CID9549225 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCO[C@@H](Cc1ccc2c(ccn2Cc2nc(-c3ccccc3Cl)oc2C)c1)C(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB047858/BDB047858.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB047858/BDB047858.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB047858/BDB047858.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB047858/BDB047858.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB047858/BDB047858.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50188029 IC50 73 nM High DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50188029 EC50 810 nM Moderate DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50188029 IC50 251 nM Moderate DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50188029 EC50 760 nM Moderate DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1