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BDBM50314833

E3L052197
Internal ID: BDB052197
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB052197/BDB052197.sdf
Basic Properties
Compound ID
E3L052197
Internal ID
BDB052197
Molecular formula
C25H25ClN2O6
Molecular weight
484.936000
Exact mass
484.140114
XLogP
5.3156
TPSA
102.1000
HBA / HBD
6 / 1
Rotatable bonds
10
Heavy atoms / rings
34 / 4
Activity summary
EC50 unknown 6.30000000 nM
4 activity record(s) imported
InChIKey
LCGZOVMJVMQILM-UHFFFAOYSA-N
SMILES
Cc1oc(-c2ccc(Cl)cc2)nc1COc1cccc(CN(CC(=O)O)C(=O)OCC2CC2)c1
Aliases
BDBM50314833 (preferred) 2-((3-((2-(4-Chlorophenyl)-5-methyloxazol-4-yl)methoxy)benzyl)((cyclopropylmethoxy)carbonyl)amino)acetic acid (source_name) BDBM50314833 (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:BDBM50314833 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50314833 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50314833 Open - 10.1021/jm9016812 PMID: 20218621
PubChem CID46196686 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1oc(-c2ccc(Cl)cc2)nc1COc1cccc(CN(CC(=O)O)C(=O)OCC2CC2)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB052197/BDB052197.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB052197/BDB052197.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB052197/BDB052197.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB052197/BDB052197.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB052197/BDB052197.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50314833 IC50 351 nM Moderate DOI: 10.1021/jm9016812
PMID: 20218621
1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50314833 EC50 6.3 nM Very high DOI: 10.1021/jm9016812
PMID: 20218621
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50314833 IC50 5336 nM Low DOI: 10.1021/jm9016812
PMID: 20218621
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50314833 EC50 826 nM Moderate DOI: 10.1021/jm9016812
PMID: 20218621
1