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BDBM50106296

E3L045873
Internal ID: BDB045873
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB045873/BDB045873.sdf
Basic Properties
Compound ID
E3L045873
Internal ID
BDB045873
Molecular formula
C21H15Cl2FN2O3
Molecular weight
433.266000
Exact mass
432.044376
XLogP
5.2615
TPSA
72.1900
HBA / HBD
3 / 1
Rotatable bonds
4
Heavy atoms / rings
29 / 4
Activity summary
IC50 unknown 1100.00000000 nM
1 activity record(s) imported
InChIKey
ZENLCDFVQUEFSK-UHFFFAOYSA-N
SMILES
O=C(O)c1ccc(-c2nc(C(=O)c3c(Cl)cccc3Cl)n3c2CCCC3)c(F)c1
Aliases
BDBM50106296 (preferred) 4-[3-(2,6-Dichlorobenzoyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-1-yl]-3-fluorobenzoic acid (source_name) BDBM50106296 (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:BDBM50106296 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50106296 Open - 10.1016/j.bmcl.2015.05.055 PMID: 26048793
PubChem CID117964950 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready O=C(O)c1ccc(-c2nc(C(=O)c3c(Cl)cccc3Cl)n3c2CCCC3)c(F)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB045873/BDB045873.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB045873/BDB045873.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB045873/BDB045873.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB045873/BDB045873.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB045873/BDB045873.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50106296 IC50 1100 nM Low DOI: 10.1016/j.bmcl.2015.05.055
PMID: 26048793
1