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BDBM50213319

E3L048632
Internal ID: BDB048632
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB048632/BDB048632.sdf
Basic Properties
Compound ID
E3L048632
Internal ID
BDB048632
Molecular formula
C25H20F3NO4
Molecular weight
455.432000
Exact mass
455.134443
XLogP
5.9027
TPSA
60.6900
HBA / HBD
3 / 1
Rotatable bonds
8
Heavy atoms / rings
33 / 4
Activity summary
IC50 > 10000.00000000 nM
2 activity record(s) imported
InChIKey
YAJRCQJLKBPIDO-UHFFFAOYSA-N
SMILES
O=C(O)Cn1ccc2cc(OCc3ccccc3COc3ccc(C(F)(F)F)cc3)ccc21
Aliases
BDBM50213319 (preferred) 2-(5-(2-((4-(trifluoromethyl)phenoxy)methyl)benzyloxy)-1H-indol-1-yl)acetic acid (source_name) BDBM50213319 (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:BDBM50213319 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50213319 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50213319 Open - 10.1016/j.bmcl.2007.04.047 PMID: 17512197
PubChem CID44432408 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready O=C(O)Cn1ccc2cc(OCc3ccccc3COc3ccc(C(F)(F)F)cc3)ccc21 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB048632/BDB048632.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB048632/BDB048632.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB048632/BDB048632.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB048632/BDB048632.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB048632/BDB048632.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50213319 IC50 >10000 nM Low DOI: 10.1016/j.bmcl.2007.04.047
PMID: 17512197
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50213319 IC50 >10000 nM Low DOI: 10.1016/j.bmcl.2007.04.047
PMID: 17512197
1