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BDBM625600

E3L031206
Internal ID: BDB031206
Activity data available Local docking-ready structure
Dock with Q9HC35
Structure
/e3_file/ligand_db/generated/BDB031206/BDB031206.sdf
Basic Properties
Compound ID
E3L031206
Internal ID
BDB031206
Molecular formula
C30H40Br2N7O2P
Molecular weight
721.479000
Exact mass
719.134784
XLogP
6.2700
TPSA
85.8600
HBA / HBD
9 / 2
Rotatable bonds
8
Heavy atoms / rings
42 / 5
Activity summary
IC50 unknown 14.00000000 nM
1 activity record(s) imported
InChIKey
KUXIUJQTRQQZQQ-UHFFFAOYSA-N
SMILES
COc1cc(N2CCC(N3CCN(C)CC3)CC2)c(Br)cc1Nc1ncc(Br)c(Nc2ccc(C)cc2P(C)(C)=O)n1
Aliases
BDBM625600 (preferred) 5-bromo-2-N-[5-bromo-2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl]-4-N-(2-dimethylphosphoryl-4-methylphenyl)pyrimidine-2,4-diamine (source_name) BDBM625600 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
Q9HC35 EML4;C2orf2;EMAPL4
Echinoderm microtubule-associated protein-like 4		 reported_binder bindingdb_reported Yes No low BindingDB:BDBM625600 medium
; target=ALK tyrosine kinase receptor
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM625600 Open - 10.7270/Q2S46X3X
PubChem CID166930852 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready COc1cc(N2CCC(N3CCN(C)CC3)CC2)c(Br)cc1Nc1ncc(Br)c(Nc2ccc(C)cc2P(C)(C)=O)n1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB031206/BDB031206.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB031206/BDB031206.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB031206/BDB031206.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB031206/BDB031206.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB031206/BDB031206.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
ALK tyrosine kinase receptor
Q9HC35
E3 ligase component 		BindingDB:BDBM625600 IC50 14 nM High DOI: 10.7270/Q2S46X3X 1