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BDBM50132566

E3L046409
Internal ID: BDB046409
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB046409/BDB046409.sdf
Basic Properties
Compound ID
E3L046409
Internal ID
BDB046409
Molecular formula
C22H21ClF3NO4
Molecular weight
455.860000
Exact mass
455.111120
XLogP
6.6097
TPSA
72.5600
HBA / HBD
4 / 1
Rotatable bonds
8
Heavy atoms / rings
31 / 3
Activity summary
Ki unknown 105.00000000 nM
4 activity record(s) imported
InChIKey
KWVHTJRFJCTACX-UHFFFAOYSA-N
SMILES
CCCc1cc2c(C(F)(F)F)noc2c(CCC)c1OC(C(=O)O)c1ccc(Cl)cc1
Aliases
BDBM50132566 (preferred) (4-Chloro-phenyl)-(5,7-dipropyl-3-trifluoromethyl-benzo[d]isoxazol-6-yloxy)-acetic acid (source_name) BDBM50132566 (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:BDBM50132566 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM50132566 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50132566 Open - 10.1016/s0960-894x(03)00702-9 PMID: 12951090
PubChem CID10276052 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCCc1cc2c(C(F)(F)F)noc2c(CCC)c1OC(C(=O)O)c1ccc(Cl)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB046409/BDB046409.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB046409/BDB046409.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB046409/BDB046409.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB046409/BDB046409.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB046409/BDB046409.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component 		BindingDB:BDBM50132566 Ki 105 nM Moderate DOI: 10.1016/s0960-894x(03)00702-9
PMID: 12951090 		2 source records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50132566 Ki 110 nM Moderate DOI: 10.1016/s0960-894x(03)00702-9
PMID: 12951090 		1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50132566 Ki 175 nM Moderate DOI: 10.1016/s0960-894x(03)00702-9
PMID: 12951090 		1