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BDBM50317117

E3L052373
Internal ID: BDB052373
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB052373/BDB052373.sdf
Basic Properties
Compound ID
E3L052373
Internal ID
BDB052373
Molecular formula
C22H21ClN2O6
Molecular weight
444.871000
Exact mass
444.108814
XLogP
4.7880
TPSA
102.1000
HBA / HBD
6 / 1
Rotatable bonds
8
Heavy atoms / rings
31 / 3
Activity summary
EC50 unknown 73.00000000 nM
2 activity record(s) imported
InChIKey
WUZGKDCLUSLLOH-AWEZNQCLSA-N
SMILES
COC(=O)N(CC(=O)O)[C@@H](C)c1cccc(OCc2coc(-c3ccc(Cl)cc3)n2)c1
Aliases
BDBM50317117 (preferred) (S)-2-((1-(3-((2-(4-chlorophenyl)oxazol-4-yl)methoxy)phenyl)ethyl)(methoxycarbonyl)amino)acetic acid (source_name) BDBM50317117 (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:BDBM50317117 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50317117 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50317117 Open - 10.1016/j.bmcl.2010.03.019 PMID: 20356736
PubChem CID46888993 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready COC(=O)N(CC(=O)O)[C@@H](C)c1cccc(OCc2coc(-c3ccc(Cl)cc3)n2)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB052373/BDB052373.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB052373/BDB052373.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB052373/BDB052373.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB052373/BDB052373.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB052373/BDB052373.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50317117 EC50 73 nM High DOI: 10.1016/j.bmcl.2010.03.019
PMID: 20356736
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50317117 EC50 >8300 nM Low DOI: 10.1016/j.bmcl.2010.03.019
PMID: 20356736
1