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BDBM788156

E3L043027
Internal ID: BDB043027
Activity data available Local docking-ready structure
Dock with P51948
Structure
/e3_file/ligand_db/generated/BDB043027/BDB043027.sdf
Basic Properties
Compound ID
E3L043027
Internal ID
BDB043027
Molecular formula
C26H34N8O
Molecular weight
474.613000
Exact mass
474.285558
XLogP
3.3722
TPSA
103.8100
HBA / HBD
7 / 4
Rotatable bonds
8
Heavy atoms / rings
35 / 6
Activity summary
IC50 unknown 226.00000000 nM
1 activity record(s) imported
InChIKey
BZQQJGZLMVFPHN-GCJKJVERSA-N
SMILES
CC(C)c1cnn2c(NCc3cn4cccc(C5CC5)c4n3)cc(NC[C@H]3CCNC[C@@H]3O)nc12
Aliases
BDBM788156 (preferred) (3R,4R)-4-[[[7-[(8-cyclopropylimidazo[1,2-a]pyridin-2-yl)methylamino]-3-propan-2-ylpyrazolo[1,5-a]pyrimidin-5-yl]amino]methyl]piperidin-3-ol (source_name) BDBM788156 (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:BDBM788156 medium
; target=Cyclin-H
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM788156 Open - 10.7270/Q2BC44B5
PubChem CID156525399 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CC(C)c1cnn2c(NCc3cn4cccc(C5CC5)c4n3)cc(NC[C@H]3CCNC[C@@H]3O)nc12 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB043027/BDB043027.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB043027/BDB043027.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB043027/BDB043027.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB043027/BDB043027.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB043027/BDB043027.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Cyclin-H
P51948
E3 ligase component 		BindingDB:BDBM788156 IC50 226 nM Moderate DOI: 10.7270/Q2BC44B5 1