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BDBM526556

E3L022629
Internal ID: BDB022629
Activity data available Local docking-ready structure
Dock with P51948
Structure
/e3_file/ligand_db/generated/BDB022629/BDB022629.sdf
Basic Properties
Compound ID
E3L022629
Internal ID
BDB022629
Molecular formula
C30H40N8O4
Molecular weight
576.702000
Exact mass
576.317252
XLogP
3.3650
TPSA
135.0100
HBA / HBD
9 / 3
Rotatable bonds
10
Heavy atoms / rings
42 / 5
Activity summary
IC50 unknown 650.00000000 nM
1 activity record(s) imported
InChIKey
UWPGYPLYDBZYFN-UHFFFAOYSA-N
SMILES
C=CC(=O)N1CCOCC1C(=O)Nc1ccc(CC)c(CNc2nc(NC3CCOCC3)nc3c(C(C)C)cnn23)c1
Aliases
BDBM526556 (preferred) 4-acryloyl-N-(4-ethyl-3-(((8-isopropyl-2-((tetrahydro-2H-pyran-4-yl)amino) pyrazolo[1,5-a][1,3,5]triazin-4-yl)amino)methyl)phenyl)morpholine-3-carboxamide (source_name) BDBM526556 (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:BDBM526556 medium
; target=Cyclin-H
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM526556 Open - 10.7270/Q2Z03CCX
PubChem CID122517747 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready C=CC(=O)N1CCOCC1C(=O)Nc1ccc(CC)c(CNc2nc(NC3CCOCC3)nc3c(C(C)C)cnn23)c1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB022629/BDB022629.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB022629/BDB022629.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB022629/BDB022629.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB022629/BDB022629.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB022629/BDB022629.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Cyclin-H
P51948
E3 ligase component 		BindingDB:BDBM526556 IC50 650 nM Moderate DOI: 10.7270/Q2Z03CCX 1