< Back to small molecule database

BDBM28719

E3L001226
Internal ID: BDB001226
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB001226/BDB001226.sdf
Basic Properties
Compound ID
E3L001226
Internal ID
BDB001226
Molecular formula
C22H23N3O4S
Molecular weight
425.510000
Exact mass
425.140927
XLogP
3.8727
TPSA
114.5400
HBA / HBD
6 / 3
Rotatable bonds
7
Heavy atoms / rings
30 / 3
Activity summary
EC50 unknown 5640.00000000 nM
2 activity record(s) imported
InChIKey
DPCYQMIKQCAHLO-UHFFFAOYSA-N
SMILES
Cc1nc(-c2ccc(N)cc2)sc1C(=O)NCc1ccc(OC(C)(C)C(=O)O)cc1
Aliases
BDBM28719 (preferred) 2-[4-({[2-(4-Aminophenyl)-4-methyl-1,3-thiazol-5-yl]formamido}methyl)phenoxy]-2-methylpropanoic acid (source_name) BDBM28719 (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:BDBM28719 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM28719 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM28719 Open - 10.1021/jm058056x PMID: 17243659
PubChem CID10295993 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1nc(-c2ccc(N)cc2)sc1C(=O)NCc1ccc(OC(C)(C)C(=O)O)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB001226/BDB001226.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB001226/BDB001226.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB001226/BDB001226.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB001226/BDB001226.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB001226/BDB001226.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM28719 EC50 5640 nM Low DOI: 10.1021/jm058056x
PMID: 17243659
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM28719 EC50 >10000 nM Low DOI: 10.1021/jm058056x
PMID: 17243659
1