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BDBM50539911

E3L059884
Internal ID: BDB059884
Activity data available Local docking-ready structure
Dock with P51948
Structure
/e3_file/ligand_db/generated/BDB059884/BDB059884.sdf
Basic Properties
Compound ID
E3L059884
Internal ID
BDB059884
Molecular formula
C26H30FN5O3S2
Molecular weight
543.690000
Exact mass
543.177410
XLogP
5.7012
TPSA
100.3600
HBA / HBD
8 / 2
Rotatable bonds
8
Heavy atoms / rings
37 / 4
Activity summary
IC50 unknown 5540.00000000 nM
1 activity record(s) imported
InChIKey
APFZUNBSYNZMFG-QGZVFWFLSA-N
SMILES
C=CC(=O)Nc1ccc(C(=O)N2CCC[C@@H](Nc3ncc(SCc4ncc(C(C)(C)C)o4)s3)C2)cc1F
Aliases
BDBM50539911 (preferred) N-[4-[(3R)-3-[[5-[(5-tert-butyl-1,3-oxazol-2-yl)methylsulfanyl]-1,3-thiazol-2-yl]amino]piperidine-1-carbonyl]-2-fluorophenyl]prop-2-enamide (source_name) BDBM50539911 (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:BDBM50539911 medium
; target=Cyclin-H
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM50539911 Open - 10.1021/acs.jmedchem.9b01929 PMID: 32502343
PubChem CID146646573 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(SCc4ncc(C(C)(C)C)o4)s3)C2)cc1F keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB059884/BDB059884.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB059884/BDB059884.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB059884/BDB059884.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB059884/BDB059884.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB059884/BDB059884.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Cyclin-H
P51948
E3 ligase component 		BindingDB:BDBM50539911 IC50 5540 nM Low DOI: 10.1021/acs.jmedchem.9b01929
PMID: 32502343 		1