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BDBM50266548

E3L050370
Internal ID: BDB050370
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB050370/BDB050370.sdf
Basic Properties
Compound ID
E3L050370
Internal ID
BDB050370
Molecular formula
C27H27NO6
Molecular weight
461.514000
Exact mass
461.183838
XLogP
5.4620
TPSA
91.7700
HBA / HBD
7 / 0
Rotatable bonds
6
Heavy atoms / rings
34 / 4
Activity summary
EC50 unknown 1740.00000000 nM
2 activity record(s) imported
InChIKey
CZWVOYZQAGCEKA-UHFFFAOYSA-N
SMILES
COC(=O)c1cc2ccc(OCCc3nc(-c4ccc(C(C)(C)C)cc4)oc3C)cc2oc1=O
Aliases
BDBM50266548 (preferred) Methyl 7-(2-(2-(4-tert-butylphenyl)-5-methyloxazol-4-yl)ethoxy)-2-oxo-2H-chromene-3-carboxylate (source_name) BDBM50266548 (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:BDBM50266548 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM50266548 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50266548 Open - 10.1016/j.ejmech.2008.01.029 PMID: 18329751
PubChem CID25148011 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready COC(=O)c1cc2ccc(OCCc3nc(-c4ccc(C(C)(C)C)cc4)oc3C)cc2oc1=O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB050370/BDB050370.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB050370/BDB050370.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB050370/BDB050370.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB050370/BDB050370.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB050370/BDB050370.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component 		BindingDB:BDBM50266548 EC50 2290 nM Low DOI: 10.1016/j.ejmech.2008.01.029
PMID: 18329751 		1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50266548 EC50 1740 nM Low DOI: 10.1016/j.ejmech.2008.01.029
PMID: 18329751 		1