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BDBM50471999

E3L057520
Internal ID: BDB057520
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB057520/BDB057520.sdf
Basic Properties
Compound ID
E3L057520
Internal ID
BDB057520
Molecular formula
C38H34N2O4
Molecular weight
582.700000
Exact mass
582.251858
XLogP
7.2256
TPSA
78.8700
HBA / HBD
5 / 2
Rotatable bonds
12
Heavy atoms / rings
44 / 6
Activity summary
Ki unknown 1622.00000000 nM
1 activity record(s) imported
InChIKey
OMWJGDTVCBGYPM-SFCXHYMASA-N
SMILES
O=C(c1ccccc1)c1ccccc1N[C@@H](Cc1ccc(OC2CCN2C(c2ccccc2)c2ccccc2)cc1)C(=O)O
Aliases
BDBM50471999 (preferred) (2S)-3-[4-(1-benzhydrylazetidin-2-yl)oxyphenyl]-2-(2-benzoylanilino)propanoic acid (source_name) BDBM50471999 (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:BDBM50471999 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50471999 Open - 10.1021/jm980413z PMID: 9836621
PubChem CID10698507 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(OC2CCN2C(c2ccccc2)c2ccccc2)cc1)C(=O)O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB057520/BDB057520.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB057520/BDB057520.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB057520/BDB057520.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB057520/BDB057520.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB057520/BDB057520.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50471999 Ki 1622 nM Low DOI: 10.1021/jm980413z
PMID: 9836621
1