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N-[[4-[(4R)-4-methyl-

E3L016394
Internal ID: BDB016394
Activity data available Local docking-ready structure
Dock with Q92793
Structure
/e3_file/ligand_db/generated/BDB016394/BDB016394.sdf
Basic Properties
Compound ID
E3L016394
Internal ID
BDB016394
Molecular formula
C18H21N3O3S
Molecular weight
359.451000
Exact mass
359.130363
XLogP
2.5454
TPSA
87.3000
HBA / HBD
4 / 3
Rotatable bonds
4
Heavy atoms / rings
25 / 3
Activity summary
IC50 unknown 387.00000000 nM
1 activity record(s) imported
InChIKey
KCYUOOTWTRKDQK-GFCCVEGCSA-N
SMILES
C[C@@H]1CC(=O)Nc2cccc(-c3ccc(CNS(C)(=O)=O)cc3)c2N1
Aliases
BDBM349472 (preferred) N-[[4-[(4R)-4-methyl- (source_name) BDBM349472 (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:BDBM349472 medium
; target=CREB-binding protein
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM349472 Open - 10.7270/Q2GM89FR
PubChem CID121278211 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready C[C@@H]1CC(=O)Nc2cccc(-c3ccc(CNS(C)(=O)=O)cc3)c2N1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB016394/BDB016394.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB016394/BDB016394.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB016394/BDB016394.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB016394/BDB016394.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB016394/BDB016394.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
CREB-binding protein
Q92793
E3 ligase component
BindingDB:BDBM349472 IC50 387 nM Moderate DOI: 10.7270/Q2GM89FR 1