< Back to small molecule database

BDBM50216944

E3L048761
Internal ID: BDB048761
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB048761/BDB048761.sdf
Basic Properties
Compound ID
E3L048761
Internal ID
BDB048761
Molecular formula
C24H25NO4
Molecular weight
391.467000
Exact mass
391.178358
XLogP
5.1661
TPSA
72.5600
HBA / HBD
4 / 1
Rotatable bonds
7
Heavy atoms / rings
29 / 4
Activity summary
EC50 unknown 2190.00000000 nM
2 activity record(s) imported
InChIKey
QCZLXHAHVYMZIL-IBGZPJMESA-N
SMILES
Cc1oc(-c2ccccc2)nc1CCOc1ccc2c(c1)CCC[C@H]2CC(=O)O
Aliases
BDBM50216944 (preferred) (S)-2-(6-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)-1,2,3,4-tetrahydronaphthalen-1-yl)acetic acid (source_name) BDBM50216944 (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:BDBM50216944 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50216944 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50216944 Open - 10.1016/j.bmcl.2007.03.057 PMID: 17601734
PubChem CID44442440 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1oc(-c2ccccc2)nc1CCOc1ccc2c(c1)CCC[C@H]2CC(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB048761/BDB048761.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB048761/BDB048761.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB048761/BDB048761.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB048761/BDB048761.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB048761/BDB048761.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50216944 EC50 2190 nM Low DOI: 10.1016/j.bmcl.2007.03.057
PMID: 17601734
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50216944 EC50 3140 nM Low DOI: 10.1016/j.bmcl.2007.03.057
PMID: 17601734
1