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BDBM50471989

E3L057510
Internal ID: BDB057510
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB057510/BDB057510.sdf
Basic Properties
Compound ID
E3L057510
Internal ID
BDB057510
Molecular formula
C34H31N3O4
Molecular weight
545.639000
Exact mass
545.231456
XLogP
6.3454
TPSA
104.3100
HBA / HBD
5 / 3
Rotatable bonds
12
Heavy atoms / rings
41 / 5
Activity summary
Ki unknown 2.60000000 nM
5 activity record(s) imported
InChIKey
SCFHGNMHMPSWDS-HKBQPEDESA-N
SMILES
Cc1[nH]c(-c2ccccc2)nc1CCOc1ccc(C[C@H](Nc2ccccc2C(=O)c2ccccc2)C(=O)O)cc1
Aliases
BDBM50471989 (preferred) (2S)-2-(2-benzoylanilino)-3-[4-[2-(5-methyl-2-phenyl-1H-imidazol-4-yl)ethoxy]phenyl]propanoic acid (source_name) BDBM50471989 (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:BDBM50471989 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50471989 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50471989 Open - 10.1021/jm980413z PMID: 9836621
PubChem CID10578478 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1[nH]c(-c2ccccc2)nc1CCOc1ccc(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/BDB057510/BDB057510.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB057510/BDB057510.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB057510/BDB057510.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB057510/BDB057510.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB057510/BDB057510.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50471989 EC50 <10000 nM Uncertain DOI: 10.1021/jm980413z
PMID: 9836621
1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50471989 Ki <3020 nM Uncertain DOI: 10.1021/jm980413z
PMID: 9836621
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50471989 EC50 380 nM Moderate DOI: 10.1021/jm980413z
PMID: 9836621
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50471989 EC50 692 nM Moderate DOI: 10.1021/jm980413z
PMID: 9836621
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50471989 Ki 2.6 nM Very high DOI: 10.1021/jm980413z
PMID: 9836621
1