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BDBM50471973

E3L057494
Internal ID: BDB057494
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB057494/BDB057494.sdf
Basic Properties
Compound ID
E3L057494
Internal ID
BDB057494
Molecular formula
C32H34N4O4S
Molecular weight
570.715000
Exact mass
570.230077
XLogP
4.8214
TPSA
103.7900
HBA / HBD
8 / 3
Rotatable bonds
12
Heavy atoms / rings
41 / 5
Activity summary
Ki unknown 4.40000000 nM
5 activity record(s) imported
InChIKey
XZIMKCMTLPLEJK-LJAQVGFWSA-N
SMILES
Cc1sc(N2CCNCC2)nc1CCOc1ccc(C[C@H](Nc2ccccc2C(=O)c2ccccc2)C(=O)O)cc1
Aliases
BDBM50471973 (preferred) (2S)-2-(2-benzoylanilino)-3-[4-[2-(5-methyl-2-piperazin-1-yl-1,3-thiazol-4-yl)ethoxy]phenyl]propanoic acid (source_name) BDBM50471973 (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:BDBM50471973 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50471973 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50471973 Open - 10.1021/jm980413z PMID: 9836621
PubChem CID10674589 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1sc(N2CCNCC2)nc1CCOc1ccc(C[C@H](Nc2ccccc2C(=O)c2ccccc2)C(=O)O)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB057494/BDB057494.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB057494/BDB057494.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB057494/BDB057494.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB057494/BDB057494.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB057494/BDB057494.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50471973 EC50 <10000 nM Uncertain DOI: 10.1021/jm980413z
PMID: 9836621
1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM50471973 Ki <3020 nM Uncertain DOI: 10.1021/jm980413z
PMID: 9836621
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50471973 EC50 117 nM Moderate DOI: 10.1021/jm980413z
PMID: 9836621
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50471973 EC50 339 nM Moderate DOI: 10.1021/jm980413z
PMID: 9836621
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50471973 Ki 4.4 nM Very high DOI: 10.1021/jm980413z
PMID: 9836621
1