BDBM808591 7-(2-fluoro-6-methyl-phenyl)-5-[(3R)- 3-(methylamino)-1- piperidyl]isoquinolin-3-amine::US12637428, Example E19

SMILES CN[C@@H]1CCCN(c2cc(-c3c(C)cccc3F)cc3cnc(N)cc23)C1

InChI Key InChIKey=WPSQPXOTPCDCFY-UHFFFAOYSA-N

Data  6 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 808591   

TargetSerine/threonine-protein kinase SIK2(Human)
Cancer Research Technology

US Patent
LigandChemical structure of BindingDB Monomer ID 808591BDBM808591(7-(2-fluoro-6-methyl-phenyl)-5-[(3R)- 3-(methylami...)
Affinity DataKi:  0.113nMAssay Description:An enzymatic assay with recombinant human CHIT1 was used in order to establish inhibitory activity of the compounds (Boot et al., 2001, JBC: 276). Th...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
1/21/2020
Entry Details
US Patent

TargetSerine/threonine-protein kinase SIK1(Human)
Cancer Research Technology

US Patent
LigandChemical structure of BindingDB Monomer ID 808591BDBM808591(7-(2-fluoro-6-methyl-phenyl)-5-[(3R)- 3-(methylami...)
Affinity DataKi:  0.476nMAssay Description:An enzymatic assay with recombinant human AMCase was used in order to establish inhibitory activity of the compounds (Boot et al., 2001, JBC: 276). T...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
1/21/2020
Entry Details
US Patent

TargetSerine/threonine-protein kinase SIK3(Human)
Cancer Research Technology

US Patent
LigandChemical structure of BindingDB Monomer ID 808591BDBM808591(7-(2-fluoro-6-methyl-phenyl)-5-[(3R)- 3-(methylami...)
Affinity DataKi:  4.45nMAssay Description:An enzymatic assay with recombinant human AMCase was used in order to establish inhibitory activity of the compounds (Boot et al., 2001, JBC: 276). T...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
1/21/2020
Entry Details
US Patent

TargetTyrosine-protein kinase ABL1(Human)
Cancer Research Technology

US Patent
LigandChemical structure of BindingDB Monomer ID 808591BDBM808591(7-(2-fluoro-6-methyl-phenyl)-5-[(3R)- 3-(methylami...)
Affinity DataKi:  24.6nMAssay Description:An enzymatic assay with recombinant human CHIT1 was used in order to establish inhibitory activity of the compounds (Boot et al., 2001, JBC: 276). Th...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
1/21/2020
Entry Details
US Patent

TargetProto-oncogene tyrosine-protein kinase Src(Human)
Cancer Research Technology

US Patent
LigandChemical structure of BindingDB Monomer ID 808591BDBM808591(7-(2-fluoro-6-methyl-phenyl)-5-[(3R)- 3-(methylami...)
Affinity DataKi:  306nMAssay Description:An enzymatic assay with recombinant human CHIT1 was used in order to establish inhibitory activity of the compounds (Boot et al., 2001, JBC: 276). Th...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
1/21/2020
Entry Details
US Patent

TargetEphrin type-A receptor 2(Human)
Cancer Research Technology

US Patent
LigandChemical structure of BindingDB Monomer ID 808591BDBM808591(7-(2-fluoro-6-methyl-phenyl)-5-[(3R)- 3-(methylami...)
Affinity DataKi: >1.00E+3nMAssay Description:An enzymatic assay with recombinant human AMCase was used in order to establish inhibitory activity of the compounds (Boot et al., 2001, JBC: 276). T...More data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
1/21/2020
Entry Details
US Patent