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BDBM50632633

E3L064425
Internal ID: BDB064425
Activity data available Local docking-ready structure
Dock with P37231
Structure
/e3_file/ligand_db/generated/BDB064425/BDB064425.sdf
Basic Properties
Compound ID
E3L064425
Internal ID
BDB064425
Molecular formula
C19H19ClIN5O2
Molecular weight
511.751000
Exact mass
511.027201
XLogP
2.8282
TPSA
96.0900
HBA / HBD
6 / 3
Rotatable bonds
5
Heavy atoms / rings
28 / 5
Activity summary
Ki unknown 1900.00000000 nM
1 activity record(s) imported
InChIKey
UKLCLLCNEQKBHK-FKQYMORYSA-N
SMILES
O[C@@H]1C[C@@H]2C[C@]2(Cn2cnc3c(NCc4cccc(I)c4)nc(Cl)nc32)[C@@H]1O
Aliases
BDBM50632633 (preferred) (1S,2S,3R,5S)-1-[[2-chloro-6-[(3-iodophenyl)methylamino]purin-9-yl]methyl]bicyclo[3.1.0]hexane-2,3-diol (source_name) BDBM50632633 (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:BDBM50632633 medium
; target=Peroxisome proliferator-activated receptor gamma
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50632633 Open - 10.1021/acs.jmedchem.2c02071 PMID: 36967575
PubChem CID172453524 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready O[C@@H]1C[C@@H]2C[C@]2(Cn2cnc3c(NCc4cccc(I)c4)nc(Cl)nc32)[C@@H]1O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB064425/BDB064425.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB064425/BDB064425.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB064425/BDB064425.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB064425/BDB064425.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB064425/BDB064425.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Peroxisome proliferator-activated receptor gamma
P37231
E3 ligase component
BindingDB:BDBM50632633 Ki 1900 nM Low DOI: 10.1021/acs.jmedchem.2c02071
PMID: 36967575
1