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BDBM50216936

E3L048753
Internal ID: BDB048753
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB048753/BDB048753.sdf
Basic Properties
Compound ID
E3L048753
Internal ID
BDB048753
Molecular formula
C26H30N2O3
Molecular weight
418.537000
Exact mass
418.225643
XLogP
5.0839
TPSA
64.3500
HBA / HBD
3 / 1
Rotatable bonds
8
Heavy atoms / rings
31 / 4
Activity summary
EC50 unknown 31.00000000 nM
2 activity record(s) imported
InChIKey
RNVUYHUTJDDRFV-NRFANRHFSA-N
SMILES
CCc1ccc(-c2nc(C)c(CCOc3ccc4c(c3)CC[C@H]4CC(=O)O)n2C)cc1
Aliases
BDBM50216936 (preferred) (S)-2-(5-(2-(2-(4-ethylphenyl)-1,4-dimethyl-1H-imidazol-5-yl)ethoxy)-2,3-dihydro-1H-inden-1-yl)acetic acid (source_name) BDBM50216936 (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:BDBM50216936 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50216936 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50216936 Open - 10.1016/j.bmcl.2007.03.057 PMID: 17601734
PubChem CID44442465 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCc1ccc(-c2nc(C)c(CCOc3ccc4c(c3)CC[C@H]4CC(=O)O)n2C)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB048753/BDB048753.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB048753/BDB048753.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB048753/BDB048753.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB048753/BDB048753.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB048753/BDB048753.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50216936 EC50 10000 nM Low DOI: 10.1016/j.bmcl.2007.03.057
PMID: 17601734
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50216936 EC50 31 nM High DOI: 10.1016/j.bmcl.2007.03.057
PMID: 17601734
1