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BDBM50205083

E3L048432
Internal ID: BDB048432
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB048432/BDB048432.sdf
Basic Properties
Compound ID
E3L048432
Internal ID
BDB048432
Molecular formula
C35H34N2O5
Molecular weight
562.666000
Exact mass
562.246772
XLogP
6.9373
TPSA
85.0300
HBA / HBD
6 / 1
Rotatable bonds
14
Heavy atoms / rings
42 / 5
Activity summary
IC50 unknown 183.00000000 nM
4 activity record(s) imported
InChIKey
ATLVKBLXBQNFLD-UHFFFAOYSA-N
SMILES
Cc1oc(-c2ccccc2)nc1CCOc1cccc(CN(CC(=O)O)Cc2ccc(OCc3ccccc3)cc2)c1
Aliases
BDBM50205083 (preferred) 2-((3-(2-(5-Methyl-2-phenyloxazol-4-yl)ethoxy)benzyl)(4-(benzyloxy)benzyl)amino)acetic acid (source_name) BDBM50205083 (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:BDBM50205083 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50205083 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50205083 Open - 10.1016/j.bmcl.2007.01.060 PMID: 17292606
PubChem CID44441451 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1oc(-c2ccccc2)nc1CCOc1cccc(CN(CC(=O)O)Cc2ccc(OCc3ccccc3)cc2)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB048432/BDB048432.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB048432/BDB048432.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB048432/BDB048432.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB048432/BDB048432.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB048432/BDB048432.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50205083 IC50 387 nM Moderate DOI: 10.1016/j.bmcl.2007.01.060
PMID: 17292606
1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50205083 EC50 324 nM Moderate DOI: 10.1016/j.bmcl.2007.01.060
PMID: 17292606
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50205083 IC50 183 nM Moderate DOI: 10.1016/j.bmcl.2007.01.060
PMID: 17292606
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50205083 EC50 412 nM Moderate DOI: 10.1016/j.bmcl.2007.01.060
PMID: 17292606
1