< Back to small molecule database

BDBM50527584

E3L059413
Internal ID: BDB059413
Activity data available Local docking-ready structure
Dock with Q09472
Structure
/e3_file/ligand_db/generated/BDB059413/BDB059413.sdf
Basic Properties
Compound ID
E3L059413
Internal ID
BDB059413
Molecular formula
C22H19F2N3O4S
Molecular weight
459.474000
Exact mass
459.106434
XLogP
4.4351
TPSA
92.6700
HBA / HBD
4 / 2
Rotatable bonds
6
Heavy atoms / rings
32 / 4
Activity summary
IC50 unknown 4000.00000000 nM
1 activity record(s) imported
InChIKey
XVUBVQJAASLZOI-UHFFFAOYSA-N
SMILES
CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cc(C)c3c(=O)[nH]ccn23)c1
Aliases
BDBM50527584 (preferred) N-[4-(2,4-difluorophenoxy)-3-(8-methyl-1-oxo-2H-pyrrolo[1,2-a]pyrazin-6-yl)phenyl]ethanesulfonamide (source_name) BDBM50527584 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
Q09472 EP300;P300
Histone acetyltransferase p300
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50527584 medium
; target=Histone acetyltransferase p300
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50527584 Open - 10.1021/acs.jmedchem.9b01784 PMID: 32208600
PubChem CID139341516 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CCS(=O)(=O)Nc1ccc(Oc2ccc(F)cc2F)c(-c2cc(C)c3c(=O)[nH]ccn23)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB059413/BDB059413.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB059413/BDB059413.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB059413/BDB059413.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB059413/BDB059413.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB059413/BDB059413.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Histone acetyltransferase p300
Q09472
E3 ligase component
BindingDB:BDBM50527584 IC50 4000 nM Low DOI: 10.1021/acs.jmedchem.9b01784
PMID: 32208600
1