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BDBM50652210

E3L065405
Internal ID: BDB065405
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB065405/BDB065405.sdf
Basic Properties
Compound ID
E3L065405
Internal ID
BDB065405
Molecular formula
C26H19NO3S2
Molecular weight
457.576000
Exact mass
457.080635
XLogP
7.2385
TPSA
46.6100
HBA / HBD
5 / 0
Rotatable bonds
5
Heavy atoms / rings
32 / 5
Activity summary
EC50 unknown 3565.00000000 nM
1 activity record(s) imported
InChIKey
HCKMTHLYPNHWOD-HAHDFKILSA-N
SMILES
Cc1ccc(CN2C(=O)S/C(=C\c3ccc(Oc4ccc5ccccc5c4)s3)C2=O)cc1
Aliases
BDBM50652210 (preferred) (5Z)-3-[(4-methylphenyl)methyl]-5-[(5-naphthalen-2-yloxythiophen-2-yl)methylidene]-1,3-thiazolidine-2,4-dione (source_name) BDBM50652210 (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:BDBM50652210 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50652210 Open - 10.7270/Q2JW8KMP PMID: 37793328
PubChem CID177372401 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1ccc(CN2C(=O)S/C(=C\c3ccc(Oc4ccc5ccccc5c4)s3)C2=O)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB065405/BDB065405.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB065405/BDB065405.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB065405/BDB065405.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB065405/BDB065405.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB065405/BDB065405.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50652210 EC50 3565 nM Low DOI: 10.7270/Q2JW8KMP
PMID: 37793328 		1