Compile Data Set for Download or QSAR

Found 43 hits of Enzyme Inhibition Constant Data   

TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM14680(2-formylphenoxyphosphonic acid | 2-formylphenyl di...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+5nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112464(CHEMBL26549 | Phosphoric acid mono-(8-hydroxy-3,4-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+5nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112470(CHEMBL279466 | Phosphoric acid mono-(2,6-diformyl-...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+5nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112456(CHEMBL287216 | Phosphoric acid mono-(4-amino-pheny...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+5nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112450(CHEMBL24656 | {[4-(benzyloxy)phenyl]amino}carbonyl...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+5nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM14679(2-formyl-6-methoxyphenoxyphosphonic acid | 2-formy...)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+5nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM24514(4-nitrophenoxyphosphonic acid | 4-nitrophenyl phos...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50080266(CHEMBL24745 | Phosphoric acid mono-naphthalen-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112452(CHEMBL25431 | Phosphoric acid mono-naphthalen-2-yl...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112460(CHEMBL24336 | Phosphoric acid mono-(4-trifluoromet...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112448(2-Phosphonooxy-benzoic acid | CHEMBL287275 | Fosfo...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112467(CHEMBL24164 | Phosphoric acid mono-p-tolyl ester)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112458(CHEMBL26438 | Phosphoric acid 2-formyl-phenyl este...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112442(CHEMBL25950 | [(3,4,5-trimethoxyphenyl)amino]carbo...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM14685((cyclohexylmethoxy)(2-formylphenoxy)phosphinic aci...)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112457(CHEMBL287306 | Phosphoric acid mono-(3-formyl-phen...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112445(CHEMBL24730 | [Hydroxy-(4-propoxy-phenyl)-methyl]-...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM14675(CHEMBL26128 | Fragment 5 | Phenylphosphate | pheno...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112454(3-Phosphonooxy-naphthalene-2-carboxylic acid methy...)copy SMILEScopy InChI
Affinity DataIC50: 3.20E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112453(CHEMBL24060 | Phosphoric acid 2-formyl-phenyl este...)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112472(CHEMBL26404 | Phosphoric acid mono-(2-chloro-pheny...)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112469(CHEMBL285775 | Phosphoric acid mono-(2-acetyl-naph...)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112461(CHEMBL26164 | {[4-(ethoxycarbonyl)phenyl]amino}car...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112462(CHEMBL24771 | [(4-butoxyphenyl)amino]carbonylphosp...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112468(4-Phosphonooxy-benzoic acid methyl ester | CHEMBL2...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112449(3-Phosphonooxy-benzoic acid methyl ester | CHEMBL2...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112440(CHEMBL26166 | {[2-(trifluoromethoxy)phenyl]amino}c...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112447(CHEMBL287555 | Phosphoric acid mono-m-tolyl ester)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112443(CHEMBL25780 | Phosphoric acid mono-(4-tert-butyl-p...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112466(CHEMBL24124 | Phosphoric acid mono-(4-methoxy-phen...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50011995((Hydroxy-naphthalen-2-yl-methyl)-phosphonic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 4.40E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112441((benzylamino)carbonylphosphonic acid | CHEMBL28727...)copy SMILEScopy InChI
Affinity DataIC50: 4.40E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM14687(CHEMBL284362 | Fragment 17 | ISO24 | [(4-ETHYLPHEN...)copy SMILEScopy InChI
Affinity DataIC50: 4.40E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112446(CHEMBL24447 | [(2-phenylethyl)amino]carbonylphosph...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM14683(CHEMBL286758 | DPI59 | Fragment 13 | [hydroxy(1-na...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+6nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112455((Hydroxy-phenyl-methyl)-phosphonic acid | Alpha Hy...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112459(CHEMBL286467 | Phosphoric acid mono-(2-cyano-8-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112439((Cyclohexyl-hydroxy-methyl)-phosphonic acid | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112451(CHEMBL26349 | Phosphoric acid mono-(2,6-dimethyl-p...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112471(CHEMBL285665 | Phosphoric acid mono-(8-hydroxy-8aH...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112465(CHEMBL24648 | [Hydroxy-(2-methoxy-phenyl)-methyl]-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112444(CHEMBL24645 | [Hydroxy-(4-isopropyl-phenyl)-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
Aventis Pharma

Curated by ChEMBL
LigandPNGBDBM50112463((Biphenyl-4-yl-hydroxy-methyl)-phosphonic acid | C...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:The compound was evaluated for its binding affinity towards phosphotyrosine binding pocket of Src protein tryrosine kinase SH2 domainMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959GW0PubMed
* indicates data uncertainty>20%