< Back to small molecule database

BDBM50157929

E3L047054
Internal ID: BDB047054
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB047054/BDB047054.sdf
Basic Properties
Compound ID
E3L047054
Internal ID
BDB047054
Molecular formula
C25H20ClNO4
Molecular weight
433.891000
Exact mass
433.108086
XLogP
5.5892
TPSA
68.5300
HBA / HBD
3 / 1
Rotatable bonds
5
Heavy atoms / rings
31 / 4
Activity summary
IC50 unknown 208.00000000 nM
1 activity record(s) imported
InChIKey
XPUQBKVFRAHDME-UHFFFAOYSA-N
SMILES
COc1ccc2c(c1)c(Cc1cccc(C(=O)O)c1)c(C)n2C(=O)c1ccc(Cl)cc1
Aliases
BDBM50157929 (preferred) 3-[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-ylmethyl]-benzoic acid (source_name) BDBM50157929 (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:BDBM50157929 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50157929 Open - 10.1016/j.bmcl.2004.10.068 PMID: 15603954
PubChem CID44389035 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready COc1ccc2c(c1)c(Cc1cccc(C(=O)O)c1)c(C)n2C(=O)c1ccc(Cl)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB047054/BDB047054.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB047054/BDB047054.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB047054/BDB047054.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB047054/BDB047054.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB047054/BDB047054.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50157929 IC50 208 nM Moderate DOI: 10.1016/j.bmcl.2004.10.068
PMID: 15603954
1