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BDBM50148477

E3L046743
Internal ID: BDB046743
Activity data available Local docking-ready structure
Dock with O15164
Structure
/e3_file/ligand_db/generated/BDB046743/BDB046743.sdf
Basic Properties
Compound ID
E3L046743
Internal ID
BDB046743
Molecular formula
C25H25N3O4S
Molecular weight
463.559000
Exact mass
463.156577
XLogP
4.3489
TPSA
82.3300
HBA / HBD
4 / 1
Rotatable bonds
5
Heavy atoms / rings
33 / 5
Activity summary
IC50 > 10000.00000000 nM
1 activity record(s) imported
InChIKey
IYDPIUJNHMAJPB-UHFFFAOYSA-N
SMILES
Cn1c(=O)n(C)c2cc(Oc3ccccc3)c(NS(=O)(=O)c3ccc4c(c3)CCCC4)cc21
Aliases
BDBM50148477 (preferred) N-(1,3-dimethyl-2-oxo-6-phenoxybenzimidazol-5-yl)-5,6,7,8-tetrahydronaphthalene-2-sulfonamide (source_name) BDBM50148477 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
O15164 TRIM24;RNF82;TIF1;TIF1A
Transcription intermediary factor 1-alpha
reported_binder bindingdb_reported Yes No low BindingDB:BDBM50148477 medium
; target=Transcription intermediary factor 1-alpha
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50148477 Open - 10.1021/acs.jmedchem.5b00458 PMID: 25974391
PubChem CID127029370 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready Cn1c(=O)n(C)c2cc(Oc3ccccc3)c(NS(=O)(=O)c3ccc4c(c3)CCCC4)cc21 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB046743/BDB046743.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB046743/BDB046743.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB046743/BDB046743.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB046743/BDB046743.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB046743/BDB046743.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Transcription intermediary factor 1-alpha
O15164
E3 ligase component
BindingDB:BDBM50148477 IC50 >10000 nM Low DOI: 10.1021/acs.jmedchem.5b00458
PMID: 25974391
1