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BDBM50334836

E3L052967
Internal ID: BDB052967
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB052967/BDB052967.sdf
Basic Properties
Compound ID
E3L052967
Internal ID
BDB052967
Molecular formula
C25H22Cl2N2O4
Molecular weight
485.367000
Exact mass
484.095663
XLogP
5.4608
TPSA
78.8700
HBA / HBD
4 / 2
Rotatable bonds
7
Heavy atoms / rings
33 / 4
Activity summary
EC50 > 30000.00000000 nM
2 activity record(s) imported
InChIKey
MRCUMHGGUAFXSG-DEOSSOPVSA-N
SMILES
Cc1cc(CN2Cc3ccccc3[C@H]2C(=O)Nc2ccc(Cl)cc2Cl)ccc1OCC(=O)O
Aliases
BDBM50334836 (preferred) [4-({(1s)-1-[(2,4-Dichlorophenyl)carbamoyl]-1,3-Dihydro-2h-Isoindol-2-Yl}methyl)-2-Methylphenoxy]acetic Acid (source_name) BDBM50334836 (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:BDBM50334836 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50334836 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50334836 Open - 10.1016/j.bmcl.2010.10.117 PMID: 21094606
PubChem CID49837873 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1cc(CN2Cc3ccccc3[C@H]2C(=O)Nc2ccc(Cl)cc2Cl)ccc1OCC(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB052967/BDB052967.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB052967/BDB052967.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB052967/BDB052967.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB052967/BDB052967.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB052967/BDB052967.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50334836 EC50 >30000 nM Low DOI: 10.1016/j.bmcl.2010.10.117
PMID: 21094606
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50334836 EC50 >30000 nM Low DOI: 10.1016/j.bmcl.2010.10.117
PMID: 21094606
1