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BDBM50135783

E3L046481
Internal ID: BDB046481
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB046481/BDB046481.sdf
Basic Properties
Compound ID
E3L046481
Internal ID
BDB046481
Molecular formula
C28H37N3O5
Molecular weight
495.620000
Exact mass
495.273321
XLogP
4.7092
TPSA
95.5800
HBA / HBD
5 / 1
Rotatable bonds
14
Heavy atoms / rings
36 / 3
Activity summary
EC50 unknown 2200.00000000 nM
2 activity record(s) imported
InChIKey
MBBHBQQBNLSENT-UHFFFAOYSA-N
SMILES
CCCCCCn1c(CCc2ccc(OC(C)(C)C(=O)O)cc2)nn(Cc2cccc(OC)c2)c1=O
Aliases
BDBM50135783 (preferred) 2-(4-{2-[4-Hexyl-1-(3-methoxy-benzyl)-5-oxo-4,5-dihydro-1H-[1,2,4]triazol-3-yl]-ethyl}-phenoxy)-2-methyl-propionic acid (source_name) BDBM50135783 (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:BDBM50135783 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM50135783 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50135783 Open - 10.1021/jm034173l PMID: 14613314
PubChem CID11156185 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCCCCCn1c(CCc2ccc(OC(C)(C)C(=O)O)cc2)nn(Cc2cccc(OC)c2)c1=O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB046481/BDB046481.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB046481/BDB046481.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB046481/BDB046481.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB046481/BDB046481.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB046481/BDB046481.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component 		BindingDB:BDBM50135783 EC50 2200 nM Low DOI: 10.1021/jm034173l
PMID: 14613314 		1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50135783 EC50 2600 nM Low DOI: 10.1021/jm034173l
PMID: 14613314 		1