< Back to small molecule database

BDBM50472003

E3L057524
Internal ID: BDB057524
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB057524/BDB057524.sdf
Basic Properties
Compound ID
E3L057524
Internal ID
BDB057524
Molecular formula
C31H29NO4
Molecular weight
479.576000
Exact mass
479.209658
XLogP
5.9553
TPSA
75.6300
HBA / HBD
4 / 2
Rotatable bonds
11
Heavy atoms / rings
36 / 4
Activity summary
Ki unknown 129.00000000 nM
1 activity record(s) imported
InChIKey
XNLIQZDQXQOJCV-LJAQVGFWSA-N
SMILES
Cc1ccccc1CCOc1ccc(C[C@H](Nc2ccccc2C(=O)c2ccccc2)C(=O)O)cc1
Aliases
BDBM50472003 (preferred) (2S)-2-(2-benzoylanilino)-3-[4-[2-(2-methylphenyl)ethoxy]phenyl]propanoic acid (source_name) BDBM50472003 (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:BDBM50472003 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50472003 Open - 10.1021/jm980413z PMID: 9836621
PubChem CID10814547 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1ccccc1CCOc1ccc(C[C@H](Nc2ccccc2C(=O)c2ccccc2)C(=O)O)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB057524/BDB057524.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB057524/BDB057524.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB057524/BDB057524.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB057524/BDB057524.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB057524/BDB057524.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50472003 Ki 129 nM Moderate DOI: 10.1021/jm980413z
PMID: 9836621
1