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BDBM50539918

E3L059891
Internal ID: BDB059891
Activity data available Local docking-ready structure
Dock with P51948
Structure
/e3_file/ligand_db/generated/BDB059891/BDB059891.sdf
Basic Properties
Compound ID
E3L059891
Internal ID
BDB059891
Molecular formula
C27H34N6O3S
Molecular weight
522.675000
Exact mass
522.241310
XLogP
4.5596
TPSA
112.3900
HBA / HBD
8 / 3
Rotatable bonds
9
Heavy atoms / rings
37 / 4
Activity summary
IC50 unknown 8870.00000000 nM
1 activity record(s) imported
InChIKey
BULBBWSMORELAY-HXUWFJFHSA-N
SMILES
C=CC(=O)Nc1ccc(C(=O)N2CCC[C@@H](Nc3ncc(CNCc4ncc(C(C)(C)C)o4)s3)C2)cc1
Aliases
BDBM50539918 (preferred) N-[4-[(3R)-3-[[5-[[(5-tert-butyl-1,3-oxazol-2-yl)methylamino]methyl]-1,3-thiazol-2-yl]amino]piperidine-1-carbonyl]phenyl]prop-2-enamide (source_name) BDBM50539918 (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:BDBM50539918 medium
; target=Cyclin-H
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50539918 Open - 10.1021/acs.jmedchem.9b01929 PMID: 32502343
PubChem CID145749889 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready C=CC(=O)Nc1ccc(C(=O)N2CCC[C@@H](Nc3ncc(CNCc4ncc(C(C)(C)C)o4)s3)C2)cc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB059891/BDB059891.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB059891/BDB059891.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB059891/BDB059891.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB059891/BDB059891.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB059891/BDB059891.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Cyclin-H
P51948
E3 ligase component 		BindingDB:BDBM50539918 IC50 8870 nM Low DOI: 10.1021/acs.jmedchem.9b01929
PMID: 32502343 		1