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BDBM530380

E3L022970
Internal ID: BDB022970
Activity data available Local docking-ready structure
Dock with P51948
Structure
/e3_file/ligand_db/generated/BDB022970/BDB022970.sdf
Basic Properties
Compound ID
E3L022970
Internal ID
BDB022970
Molecular formula
C31H37N5O2
Molecular weight
511.670000
Exact mass
511.294725
XLogP
4.1140
TPSA
70.5900
HBA / HBD
6 / 1
Rotatable bonds
7
Heavy atoms / rings
38 / 6
Activity summary
IC50 unknown 6.31000000 nM
2 activity record(s) imported
InChIKey
ANXJNRMEWJLRAK-KKVCJECGSA-N
SMILES
C[C@@H]1Cc2cnc(NCc3ccccc3)nc2CN1C(=O)[C@H]1CCN(CC2COC2)C[C@@H]1c1ccccc1
Aliases
BDBM530380 (preferred) [(6R)-2-(benzylamino)-6-methyl-6,8-dihydro-5H-pyrido[3,4-d]pyrimidin-7-yl]-[(3S,4S)-1-(oxetan-3-ylmethyl)-3-phenylpiperidin-4-yl]methanone (source_name) BDBM530380 (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:BDBM530380 medium
; target=Cyclin-H
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM530380 Open - 10.7270/Q2MC936B
PubChem CID163200310 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready C[C@@H]1Cc2cnc(NCc3ccccc3)nc2CN1C(=O)[C@H]1CCN(CC2COC2)C[C@@H]1c1ccccc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB022970/BDB022970.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB022970/BDB022970.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB022970/BDB022970.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB022970/BDB022970.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB022970/BDB022970.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Cyclin-H
P51948
E3 ligase component 		BindingDB:BDBM530380 IC50 <9.77 nM Very high DOI: 10.7270/Q2MC936B 1
Cyclin-H
P51948
E3 ligase component 		BindingDB:BDBM530380 IC50 6.31 nM Very high DOI: 10.7270/Q2MC936B 1