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BDBM50188032

E3L047861
Internal ID: BDB047861
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB047861/BDB047861.sdf
Basic Properties
Compound ID
E3L047861
Internal ID
BDB047861
Molecular formula
C26H25F3N2O4
Molecular weight
486.490000
Exact mass
486.176642
XLogP
6.0941
TPSA
77.4900
HBA / HBD
4 / 1
Rotatable bonds
9
Heavy atoms / rings
35 / 4
Activity summary
IC50 unknown 40.00000000 nM
4 activity record(s) imported
InChIKey
SNELYVVCHDOVFP-UHFFFAOYSA-N
SMILES
CCCOC(Cc1ccc2c(ccn2Cc2nc(-c3ccc(C(F)(F)F)cc3)oc2C)c1)C(=O)O
Aliases
BDBM50188032 (preferred) 3-(1-((5-methyl-2-(4-(trifluoromethyl)phenyl)oxazol-4-yl)methyl)-1H-indol-5-yl)-2-propoxypropanoic acid (source_name) BDBM50188032 (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:BDBM50188032 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50188032 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50188032 Open - 10.1016/j.bmcl.2006.05.007 PMID: 16737814
PubChem CID10254845 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCCOC(Cc1ccc2c(ccn2Cc2nc(-c3ccc(C(F)(F)F)cc3)oc2C)c1)C(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB047861/BDB047861.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB047861/BDB047861.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB047861/BDB047861.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB047861/BDB047861.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB047861/BDB047861.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50188032 IC50 40 nM High DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50188032 EC50 510 nM Moderate DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50188032 IC50 399 nM Moderate DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50188032 EC50 2000 nM Low DOI: 10.1016/j.bmcl.2006.05.007
PMID: 16737814
1