Compile Data Set for Download or QSAR

Found 7 hits of Enzyme Inhibition Constant Data   

TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Rhode Island

Curated by ChEMBL
LigandPNGBDBM50101077((1S,4S)-2-((S)-2-{(S)-2-[2-Amino-3-(4-phosphonooxy...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+3nMAssay Description:Inhibitory concentration against Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W37VWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Rhode Island

Curated by ChEMBL
LigandPNGBDBM50174137((S)-4-[(S)-2-((2S,3S)-2-Amino-3-methyl-pentanoylam...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W37VWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Rhode Island

Curated by ChEMBL
LigandPNGBDBM50174138((S)-4-[(S)-2-((1S,4S)-2-Amino-3-methyl-pentanoylam...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W37VWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Rhode Island

Curated by ChEMBL
LigandPNGBDBM50174134((2S,3S)-2-{(S)-2-[(S)-2-((S)-2-Amino-3-phenyl-prop...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W37VWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Rhode Island

Curated by ChEMBL
LigandPNGBDBM50174135((2S,3S)-2-((S)-2-{(S)-2-[(S)-2-Amino-3-(4-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W37VWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Rhode Island

Curated by ChEMBL
LigandPNGBDBM50174136((S)-4-[(S)-2-((2S,3S)-2-Amino-3-methyl-pentanoylam...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W37VWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Rhode Island

Curated by ChEMBL
LigandPNGBDBM50101077((1S,4S)-2-((S)-2-{(S)-2-[2-Amino-3-(4-phosphonooxy...)copy SMILEScopy InChI
Affinity DataKd:  100nMAssay Description:Dissociation constant against Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2W37VWCPubMed
* indicates data uncertainty>20%