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BDBM50426770

E3L055669
Internal ID: BDB055669
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB055669/BDB055669.sdf
Basic Properties
Compound ID
E3L055669
Internal ID
BDB055669
Molecular formula
C28H29N7O
Molecular weight
479.588000
Exact mass
479.243359
XLogP
4.7991
TPSA
94.2800
HBA / HBD
5 / 1
Rotatable bonds
6
Heavy atoms / rings
36 / 6
Activity summary
EC50 unknown 1710.00000000 nM
1 activity record(s) imported
InChIKey
BRVNNIGOENBZSY-DEOSSOPVSA-N
SMILES
CCc1nc2ccn(CC(C)C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21
Aliases
BDBM50426770 (preferred) 2-ethyl-5-(2-methylpropyl)-3-[(1S)-5-[2-(2H-tetrazol-5-yl)phenyl]-2,3-dihydro-1H-inden-1-yl]imidazo[4,5-c]pyridin-4-one (source_name) BDBM50426770 (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:BDBM50426770 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50426770 Open - 10.1016/j.bmcl.2012.11.088 PMID: 23265881
PubChem CID71521299 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCc1nc2ccn(CC(C)C)c(=O)c2n1[C@H]1CCc2cc(-c3ccccc3-c3nnn[nH]3)ccc21 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB055669/BDB055669.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB055669/BDB055669.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB055669/BDB055669.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB055669/BDB055669.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB055669/BDB055669.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50426770 EC50 1710 nM Low DOI: 10.1016/j.bmcl.2012.11.088
PMID: 23265881
1