< Back to small molecule database

BDBM50527592

E3L059420
Internal ID: BDB059420
Activity data available Local docking-ready structure
Dock with Q09472
Structure
/e3_file/ligand_db/generated/BDB059420/BDB059420.sdf
Basic Properties
Compound ID
E3L059420
Internal ID
BDB059420
Molecular formula
C21H19N3O4S
Molecular weight
409.467000
Exact mass
409.109627
XLogP
3.7668
TPSA
92.6700
HBA / HBD
4 / 2
Rotatable bonds
5
Heavy atoms / rings
29 / 4
Activity summary
IC50 unknown 25100.00000000 nM
1 activity record(s) imported
InChIKey
RZNRDMSSIKQWGN-UHFFFAOYSA-N
SMILES
Cc1cc(-c2cc(NS(C)(=O)=O)ccc2Oc2ccccc2)n2cc[nH]c(=O)c12
Aliases
BDBM50527592 (preferred) N-[3-(8-methyl-1-oxidanylidene-2H-pyrrolo[1,2-a]pyrazin-6-yl)-4-phenoxy-phenyl]methanesulfonamide (source_name) BDBM50527592 (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:BDBM50527592 medium
; target=Histone acetyltransferase p300
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50527592 Open - 10.1021/acs.jmedchem.9b01784 PMID: 32208600
PubChem CID139341527 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cc1cc(-c2cc(NS(C)(=O)=O)ccc2Oc2ccccc2)n2cc[nH]c(=O)c12 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB059420/BDB059420.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB059420/BDB059420.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB059420/BDB059420.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB059420/BDB059420.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB059420/BDB059420.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Histone acetyltransferase p300
Q09472
E3 ligase component 		BindingDB:BDBM50527592 IC50 25100 nM Low DOI: 10.1021/acs.jmedchem.9b01784
PMID: 32208600 		1