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BDBM50133665

E3L046443
Internal ID: BDB046443
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB046443/BDB046443.sdf
Basic Properties
Compound ID
E3L046443
Internal ID
BDB046443
Molecular formula
C26H31NO6
Molecular weight
453.535000
Exact mass
453.215138
XLogP
5.0349
TPSA
93.9200
HBA / HBD
6 / 2
Rotatable bonds
10
Heavy atoms / rings
33 / 4
Activity summary
IC50 unknown 750.00000000 nM
3 activity record(s) imported
InChIKey
NQHKVVYCDHWYMA-UHFFFAOYSA-N
SMILES
CCCc1cc(C2CCOCC2)ccc1OCCCOc1cccc(-c2oc(=O)[nH]c2O)c1
Aliases
BDBM50133665 (preferred) 5-(3-{3-[2-Propyl-4-(tetrahydro-pyran-4-yl)-phenoxy]-propoxy}-phenyl)-oxazolidine-2,4-dione (source_name) BDBM50133665 (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:BDBM50133665 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50133665 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50133665 Open - 10.1016/s0960-894x(03)00785-6; 10.1016/j.ejmech.2011.03.040 PMID: 14505666; 21482446
PubChem CID91182856 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCCc1cc(C2CCOCC2)ccc1OCCCOc1cccc(-c2oc(=O)[nH]c2O)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB046443/BDB046443.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB046443/BDB046443.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB046443/BDB046443.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB046443/BDB046443.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB046443/BDB046443.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50133665 IC50 2880 nM Low DOI: 10.1016/s0960-894x(03)00785-6
PMID: 14505666
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50133665 IC50 750 nM Moderate DOI: 10.1016/j.ejmech.2011.03.040
PMID: 21482446
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50133665 IC50 750 nM Moderate DOI: 10.1016/s0960-894x(03)00785-6
PMID: 14505666
1