null

SMILES CCN1CCC(CC1)n1nc(Cc2cccc3ccccc23)c2c(N)ncnc12

InChI Key InChIKey=BSGWEWBSWAVORO-UHFFFAOYSA-N

  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 4 hits for monomerid = 50345717   

TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
University of Washington Through its Center for Commercialization

US Patent
LigandPNGBDBM50345717(1-(1-ethylpiperidin-4-yl)-3-(naphthalen-1-ylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 360nMAssay Description:Inhibition of human tyrosine kinases.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56MVCUS Patent
TargetCalmodulin-domain protein kinase 1(Toxoplasma gondii)
University of Washington Through its Center for Commercialization

US Patent
LigandPNGBDBM50345717(1-(1-ethylpiperidin-4-yl)-3-(naphthalen-1-ylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Most known kinase inhibitors bind in the ATP-binding pocket of the active site19,20. These inhibitors exploit many of the same hydrophobic contacts a...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56MVCUS Patent
TargetCalcium-dependent protein kinase 1(Cryptosporidium parvum)
University of Washington Through its Center for Commercialization

US Patent
LigandPNGBDBM50345717(1-(1-ethylpiperidin-4-yl)-3-(naphthalen-1-ylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Two types of enzyme assays were developed to follow TgCDPK1 activity, a radiometric scintillation proximity assay measured the labeled γ-phospha...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56MVCUS Patent
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Washington Through its Center for Commercialization

US Patent
LigandPNGBDBM50345717(1-(1-ethylpiperidin-4-yl)-3-(naphthalen-1-ylmethyl...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibition of human tyrosine kinases.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2B56MVCUS Patent