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BDBM50344227

E3L053278
Internal ID: BDB053278
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB053278/BDB053278.sdf
Basic Properties
Compound ID
E3L053278
Internal ID
BDB053278
Molecular formula
C29H34N2O5
Molecular weight
490.600000
Exact mass
490.246772
XLogP
6.9760
TPSA
98.5900
HBA / HBD
6 / 1
Rotatable bonds
11
Heavy atoms / rings
36 / 4
Activity summary
EC50 unknown 2600.00000000 nM
2 activity record(s) imported
InChIKey
TYNRGESLBOBNOI-UHFFFAOYSA-N
SMILES
CCCCc1ccc(-c2nc(CCc3noc4cc(OC(C)(C)C(=O)O)ccc34)c(C(C)C)o2)cc1
Aliases
BDBM50344227 (preferred) 2-[3-[2-[2-(4-Butylphenyl)-5-isopropyl-4-oxazolyl]ethyl]-1,2-benzisoxazol-6-yloxy]-2-methylpropionic acid (source_name) BDBM50344227 (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:BDBM50344227 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50344227 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50344227 Open - 10.1016/j.bmc.2011.03.053 PMID: 21515063
PubChem CID54585711 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCCCc1ccc(-c2nc(CCc3noc4cc(OC(C)(C)C(=O)O)ccc34)c(C(C)C)o2)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB053278/BDB053278.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB053278/BDB053278.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB053278/BDB053278.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB053278/BDB053278.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB053278/BDB053278.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50344227 EC50 3300 nM Low DOI: 10.1016/j.bmc.2011.03.053
PMID: 21515063
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50344227 EC50 2600 nM Low DOI: 10.1016/j.bmc.2011.03.053
PMID: 21515063
1