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BDBM28752

E3L001234
Internal ID: BDB001234
Activity data available Local docking-ready structure
Dock with P37231 Dock with Q07869
Structure
/e3_file/ligand_db/generated/BDB001234/BDB001234.sdf
Basic Properties
Compound ID
E3L001234
Internal ID
BDB001234
Molecular formula
C20H19ClN2O3S2
Molecular weight
434.970000
Exact mass
434.052562
XLogP
5.7012
TPSA
72.3100
HBA / HBD
6 / 1
Rotatable bonds
7
Heavy atoms / rings
28 / 3
Activity summary
EC50 unknown 186.00000000 nM
4 activity record(s) imported
InChIKey
CHWARMCOUPSGEK-UHFFFAOYSA-N
SMILES
Cc1cc(SCc2nc(-c3ccc(Cl)cc3)ns2)ccc1OC(C)(C)C(=O)O
Aliases
BDBM28752 (preferred) 2-[4-({[3-(4-Chlorophenyl)-1,2,4-thiadiazol-5-yl]methyl}sulfanyl)-2-methylphenoxy]-2-methylpropanoic acid (source_name) BDBM28752 (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:BDBM28752 medium
; target=Peroxisome proliferator-activated receptor gamma
Q07869 PPARA;NR1C1;PPAR
Peroxisome proliferator-activated receptor alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM28752 medium
; target=Peroxisome proliferator-activated receptor alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM28752 Open - 10.1021/jm070511x; 10.1016/j.bmc.2007.12.005 PMID: 17608467; 18155554
PubChem CID11235892 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1cc(SCc2nc(-c3ccc(Cl)cc3)ns2)ccc1OC(C)(C)C(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB001234/BDB001234.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB001234/BDB001234.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB001234/BDB001234.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB001234/BDB001234.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB001234/BDB001234.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM28752 EC50 186 nM Moderate DOI: 10.1016/j.bmc.2007.12.005
PMID: 18155554
1
Peroxisome proliferator-activated receptor alpha
Q07869
E3 ligase component
BindingDB:BDBM28752 EC50 186 nM Moderate DOI: 10.1021/jm070511x
PMID: 17608467
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM28752 EC50 >3000 nM Low DOI: 10.1016/j.bmc.2007.12.005
PMID: 18155554
1
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM28752 EC50 >3000 nM Low DOI: 10.1021/jm070511x
PMID: 17608467
1