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US20240166635, Example 86

E3L033751
Internal ID: BDB033751
Activity data available Local docking-ready structure
Dock with P51948
Structure
/e3_file/ligand_db/generated/BDB033751/BDB033751.sdf
Basic Properties
Compound ID
E3L033751
Internal ID
BDB033751
Molecular formula
C15H18FN5O2S
Molecular weight
351.407000
Exact mass
351.116524
XLogP
1.9970
TPSA
101.2100
HBA / HBD
6 / 2
Rotatable bonds
4
Heavy atoms / rings
24 / 3
Activity summary
IC50 > 1000.00000000 nM
1 activity record(s) imported
InChIKey
FTJDGUPVEVBZFA-UHFFFAOYSA-N
SMILES
NS(=O)(=O)c1ccc(Nc2ncc(F)c(N3CCCCC3)n2)cc1
Aliases
BDBM676366 (preferred) US20240166635, Example 86 (source_name) BDBM676366 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
P51948 MNAT1;CAP35;MAT1;RNF66
CDK-activating kinase assembly factor MAT1
reported_binder bindingdb_reported Yes No low BindingDB:BDBM676366 medium
; target=Cyclin-H
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM676366 Open - 10.7270/Q2GM8CMT
PubChem CID167090155 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready NS(=O)(=O)c1ccc(Nc2ncc(F)c(N3CCCCC3)n2)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB033751/BDB033751.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB033751/BDB033751.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB033751/BDB033751.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB033751/BDB033751.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB033751/BDB033751.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Cyclin-H
P51948
E3 ligase component
BindingDB:BDBM676366 IC50 >1000 nM Moderate DOI: 10.7270/Q2GM8CMT 1