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BDBM50471986

E3L057507
Internal ID: BDB057507
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB057507/BDB057507.sdf
Basic Properties
Compound ID
E3L057507
Internal ID
BDB057507
Molecular formula
C33H28N2O4S
Molecular weight
548.664000
Exact mass
548.176978
XLogP
6.7704
TPSA
88.5200
HBA / HBD
6 / 2
Rotatable bonds
12
Heavy atoms / rings
40 / 5
Activity summary
Ki unknown 1445.00000000 nM
1 activity record(s) imported
InChIKey
WHXOFSYNZVGELV-LJAQVGFWSA-N
SMILES
O=C(c1ccccc1)c1ccccc1N[C@@H](Cc1ccc(OCCc2scnc2-c2ccccc2)cc1)C(=O)O
Aliases
BDBM50471986 (preferred) (2S)-2-(2-benzoylanilino)-3-[4-[2-(4-phenyl-1,3-thiazol-5-yl)ethoxy]phenyl]propanoic acid (source_name) BDBM50471986 (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:BDBM50471986 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50471986 Open - 10.1021/jm980413z PMID: 9836621
PubChem CID10674186 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready O=C(c1ccccc1)c1ccccc1N[C@@H](Cc1ccc(OCCc2scnc2-c2ccccc2)cc1)C(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB057507/BDB057507.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB057507/BDB057507.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB057507/BDB057507.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB057507/BDB057507.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB057507/BDB057507.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component 		BindingDB:BDBM50471986 Ki 1445 nM Low DOI: 10.1021/jm980413z
PMID: 9836621 		1