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4-methyl-N-[3-(4-methyl-

E3L016332
Internal ID: BDB016332
Activity data available Local docking-ready structure
Dock with Q92793
Structure
/e3_file/ligand_db/generated/BDB016332/BDB016332.sdf
Basic Properties
Compound ID
E3L016332
Internal ID
BDB016332
Molecular formula
C20H20N6O2
Molecular weight
376.420000
Exact mass
376.164774
XLogP
2.8770
TPSA
100.9400
HBA / HBD
5 / 3
Rotatable bonds
3
Heavy atoms / rings
28 / 4
Activity summary
IC50 unknown 403.00000000 nM
1 activity record(s) imported
InChIKey
DSPRUHNYLWDVCX-UHFFFAOYSA-N
SMILES
CC1CC(=O)Nc2cccc(C(=O)Nc3cccc(-c4nncn4C)c3)c2N1
Aliases
BDBM349410 (preferred) 4-methyl-N-[3-(4-methyl- (source_name) BDBM349410 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
Q92793 CREBBP;CBP
CREB-binding protein
reported_binder bindingdb_reported Yes No low BindingDB:BDBM349410 medium
; target=CREB-binding protein
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM349410 Open - 10.7270/Q2GM89FR
PubChem CID121278106 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CC1CC(=O)Nc2cccc(C(=O)Nc3cccc(-c4nncn4C)c3)c2N1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB016332/BDB016332.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB016332/BDB016332.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB016332/BDB016332.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB016332/BDB016332.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB016332/BDB016332.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
CREB-binding protein
Q92793
E3 ligase component
BindingDB:BDBM349410 IC50 403 nM Moderate DOI: 10.7270/Q2GM89FR 1