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US10155764, Example 14B

E3L013668
Internal ID: BDB013668
Activity data available Local docking-ready structure
Dock with Q92831
Structure
/e3_file/ligand_db/generated/BDB013668/BDB013668.sdf
Basic Properties
Compound ID
E3L013668
Internal ID
BDB013668
Molecular formula
C14H19N5O
Molecular weight
273.340000
Exact mass
273.158960
XLogP
1.0103
TPSA
85.8300
HBA / HBD
5 / 2
Rotatable bonds
2
Heavy atoms / rings
20 / 3
Activity summary
IC50 unknown 1500.00000000 nM
1 activity record(s) imported
InChIKey
YMSYHVGICLNROS-MNOVXSKESA-N
SMILES
Cn1nc(N[C@H]2CCCC[C@H]2N)c2ncccc2c1=O
Aliases
BDBM311421 (preferred) US10155764, Example 14B (source_name) BDBM311421 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
Q92831 KAT2B;PCAF
Histone acetyltransferase KAT2B
reported_binder bindingdb_reported Yes No low BindingDB:BDBM311421 medium
; target=Histone acetyltransferase KAT2B
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM311421 Open - 10.7270/Q25M67T9
PubChem CID118928658 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cn1nc(N[C@H]2CCCC[C@H]2N)c2ncccc2c1=O keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB013668/BDB013668.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB013668/BDB013668.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB013668/BDB013668.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB013668/BDB013668.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB013668/BDB013668.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Histone acetyltransferase KAT2B
Q92831
E3 ligase component
BindingDB:BDBM311421 IC50 1500 nM Low DOI: 10.7270/Q25M67T9 1