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BDBM50121424

E3L046123
Internal ID: BDB046123
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB046123/BDB046123.sdf
Basic Properties
Compound ID
E3L046123
Internal ID
BDB046123
Molecular formula
C18H10Cl3N3O4
Molecular weight
438.654000
Exact mass
436.973689
XLogP
5.1796
TPSA
101.4100
HBA / HBD
5 / 2
Rotatable bonds
5
Heavy atoms / rings
28 / 3
Activity summary
Ki unknown 160.00000000 nM
4 activity record(s) imported
InChIKey
OSSVQVKVEZPBSO-UHFFFAOYSA-N
SMILES
O=C(Nc1ccc(Oc2cncc(Cl)n2)cc1C(=O)O)c1ccc(Cl)cc1Cl
Aliases
BDBM50121424 (preferred) 5-(6-Chloropyrazin-2-yl)oxy-2-[(2,4-dichlorobenzoyl)amino]benzoic acid (source_name) BDBM50121424 (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:BDBM50121424 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM50121424 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50121424 Open - 10.1016/s0960-894x(02)00791-6 PMID: 12443777
PubChem CID10296909 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready O=C(Nc1ccc(Oc2cncc(Cl)n2)cc1C(=O)O)c1ccc(Cl)cc1Cl keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB046123/BDB046123.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB046123/BDB046123.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB046123/BDB046123.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB046123/BDB046123.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB046123/BDB046123.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component 		BindingDB:BDBM50121424 EC50 >100000 nM Low DOI: 10.1016/s0960-894x(02)00791-6
PMID: 12443777 		1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component 		BindingDB:BDBM50121424 Ki 21000 nM Low DOI: 10.1016/s0960-894x(02)00791-6
PMID: 12443777 		1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50121424 EC50 450 nM Moderate DOI: 10.1016/s0960-894x(02)00791-6
PMID: 12443777 		1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50121424 Ki 160 nM Moderate DOI: 10.1016/s0960-894x(02)00791-6
PMID: 12443777 		1