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BDBM147424

E3L006533
Internal ID: BDB006533
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB006533/BDB006533.sdf
Basic Properties
Compound ID
E3L006533
Internal ID
BDB006533
Molecular formula
C32H28ClN3O3
Molecular weight
538.047000
Exact mass
537.181919
XLogP
7.2110
TPSA
84.2200
HBA / HBD
3 / 2
Rotatable bonds
7
Heavy atoms / rings
39 / 5
Activity summary
IC50 unknown 144.00000000 nM
1 activity record(s) imported
InChIKey
FHWUAKZRPWCAON-FQEVSTJZSA-N
SMILES
Cc1c(C)n(Cc2ccc(-c3ccccc3C(=O)O)cc2)c2ccc(C(=O)N[C@@H](C)c3ccc(Cl)nc3)cc12
Aliases
BDBM147424 (preferred) 2-[4-[[5-[[(1S)-1-(6-chloro-3-pyridinyl)ethyl]carbamoyl]-2,3-dimethylindol-1-yl]methyl]phenyl]benzoic acid (source_name) BDBM147424 (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:BDBM147424 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM147424 Open - 10.7270/Q2X63KNR
PubChem CID89251903 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1c(C)n(Cc2ccc(-c3ccccc3C(=O)O)cc2)c2ccc(C(=O)N[C@@H](C)c3ccc(Cl)nc3)cc12 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB006533/BDB006533.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB006533/BDB006533.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB006533/BDB006533.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB006533/BDB006533.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB006533/BDB006533.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM147424 IC50 144 nM Moderate DOI: 10.7270/Q2X63KNR 1