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BDBM530283

E3L022883
Internal ID: BDB022883
Activity data available Local docking-ready structure
Dock with P51948
Structure
/e3_file/ligand_db/generated/BDB022883/BDB022883.sdf
Basic Properties
Compound ID
E3L022883
Internal ID
BDB022883
Molecular formula
C28H31F2N5O
Molecular weight
491.586000
Exact mass
491.249667
XLogP
4.3756
TPSA
61.3600
HBA / HBD
5 / 1
Rotatable bonds
5
Heavy atoms / rings
36 / 5
Activity summary
IC50 unknown 13.00000000 nM
1 activity record(s) imported
InChIKey
FCALXDFJLVUWIQ-RZFNWQHOSA-N
SMILES
C[C@@H]1Cc2cnc(NCc3c(F)cccc3F)nc2CN1C(=O)[C@H]1CCN(C)C[C@@H]1c1ccccc1
Aliases
BDBM530283 (preferred) [(6R)-2-[(2,6-difluorophenyl)methylamino]-6-methyl-6,8-dihydro-5H-pyrido[3,4-d]pyrimidin-7-yl]-[(3S,4S)-1-methyl-3-phenylpiperidin-4-yl]methanone (source_name) BDBM530283 (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:BDBM530283 medium
; target=Cyclin-H
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM530283 Open - 10.7270/Q2MC936B
PubChem CID163200224 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready C[C@@H]1Cc2cnc(NCc3c(F)cccc3F)nc2CN1C(=O)[C@H]1CCN(C)C[C@@H]1c1ccccc1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB022883/BDB022883.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB022883/BDB022883.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB022883/BDB022883.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB022883/BDB022883.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB022883/BDB022883.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Cyclin-H
P51948
E3 ligase component 		BindingDB:BDBM530283 IC50 13 nM High DOI: 10.7270/Q2MC936B 1