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BDBM50344223

E3L053274
Internal ID: BDB053274
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB053274/BDB053274.sdf
Basic Properties
Compound ID
E3L053274
Internal ID
BDB053274
Molecular formula
C28H31ClN2O5
Molecular weight
511.018000
Exact mass
510.192150
XLogP
7.2862
TPSA
98.5900
HBA / HBD
6 / 1
Rotatable bonds
12
Heavy atoms / rings
36 / 4
Activity summary
EC50 unknown 2300.00000000 nM
2 activity record(s) imported
InChIKey
PZNVHYMAMHJHPX-UHFFFAOYSA-N
SMILES
CCCCCCc1oc(-c2ccccc2Cl)nc1CCc1noc2cc(OC(C)(C)C(=O)O)ccc12
Aliases
BDBM50344223 (preferred) 2-[3-[2-[2-(2-Chlorophenyl)-5-hexyl-4-oxazolyl]ethyl]-1,2-benzisoxazol-6-yloxy]-2-methylpropionic acid (source_name) BDBM50344223 (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:BDBM50344223 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM50344223 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50344223 Open - 10.1016/j.bmc.2011.03.053 PMID: 21515063
PubChem CID54580814 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCCCCCc1oc(-c2ccccc2Cl)nc1CCc1noc2cc(OC(C)(C)C(=O)O)ccc12 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB053274/BDB053274.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB053274/BDB053274.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB053274/BDB053274.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB053274/BDB053274.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB053274/BDB053274.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component 		BindingDB:BDBM50344223 EC50 2300 nM Low DOI: 10.1016/j.bmc.2011.03.053
PMID: 21515063 		1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50344223 EC50 5900 nM Low DOI: 10.1016/j.bmc.2011.03.053
PMID: 21515063 		1