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BDBM513845

E3L021363
Internal ID: BDB021363
Activity data available Local docking-ready structure
Dock with O75530 Dock with Q09028
Structure
/e3_file/ligand_db/generated/BDB021363/BDB021363.sdf
Basic Properties
Compound ID
E3L021363
Internal ID
BDB021363
Molecular formula
C26H24FN5O3
Molecular weight
473.508000
Exact mass
473.186318
XLogP
4.2877
TPSA
93.7000
HBA / HBD
7 / 1
Rotatable bonds
8
Heavy atoms / rings
35 / 5
Activity summary
IC50 unknown 300.00000000 nM
10 activity record(s) imported
InChIKey
DUXYHMYBFJIRAW-UHFFFAOYSA-N
SMILES
COCCOc1ccc(-c2cnc(NCc3c(F)ccc4c3CCO4)n3cc(C#N)nc23)c(C)c1
Aliases
BDBM513845 (preferred) 5-(((5-Fluoro-2,3-dihydrobenzofuran-4-yl)methyl)amino)-8-(4-(2-methoxyethoxy)-2-methylphenyl)imidazo[1,2-c]pyrimidine-2-carbonitrile (source_name) BDBM513845 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
O75530 EED
Polycomb protein EED
reported_binder bindingdb_reported Yes No low BindingDB:BDBM513845 medium
; target=Histone-lysine N-methyltransferase EZH2; Polycomb protein EED
Q09028 RBBP4;RBAP48
Histone-binding protein RBBP4
reported_binder bindingdb_reported Yes No low BindingDB:BDBM513845 medium
; target=Histone-lysine N-methyltransferase EZH2; Polycomb protein EED
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM513845 Open - 10.7270/Q2V69NQ4; 10.7270/Q2J969K9; 10.7270/Q2HQ43R4
PubChem CID139371008 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready COCCOc1ccc(-c2cnc(NCc3c(F)ccc4c3CCO4)n3cc(C#N)nc23)c(C)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB021363/BDB021363.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB021363/BDB021363.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB021363/BDB021363.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB021363/BDB021363.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB021363/BDB021363.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Histone-lysine N-methyltransferase EZH2
Q09028
E3 ligase component
BindingDB:BDBM513845 IC50 300 nM Moderate DOI: 10.7270/Q2V69NQ4 1
Histone-lysine N-methyltransferase EZH2
O75530
E3 ligase component
BindingDB:BDBM513845 IC50 300 nM Moderate DOI: 10.7270/Q2J969K9 3 source records
Histone-lysine N-methyltransferase EZH2
Q09028
E3 ligase component
BindingDB:BDBM513845 IC50 300 nM Moderate DOI: 10.7270/Q2J969K9 3 source records
Histone-lysine N-methyltransferase EZH2
O75530
E3 ligase component
BindingDB:BDBM513845 IC50 300 nM Moderate DOI: 10.7270/Q2V69NQ4 1
Polycomb protein EED
Q09028
E3 ligase component
BindingDB:BDBM513845 IC50 300 nM Moderate DOI: 10.7270/Q2HQ43R4 1
Polycomb protein EED
O75530
E3 ligase component
BindingDB:BDBM513845 IC50 300 nM Moderate DOI: 10.7270/Q2HQ43R4 1