Compile Data Set for Download or QSAR
Found 292 with Last Name = 'green' and Initial = 't'
Target5-hydroxytryptamine receptor 3A(Mus musculus (house mouse))
Medical Research Council Centre

Curated by PDSP Ki Database
LigandPNGBDBM82473(CAS_124006 | GR 65630 | NSC_124006)copy SMILEScopy InChI
Affinity DataKi:  0.210nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9GR6PubMed
Target5-hydroxytryptamine receptor 3A(Mus musculus (house mouse))
Medical Research Council Centre

Curated by PDSP Ki Database
LigandPNGBDBM82474(1-(3-CHLOROPHENYL)BIGUANIDE HYDROCHLORIDE | CAS_21...)copy SMILEScopy InChI
Affinity DataKi:  0.940nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9GR6PubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM50252103((2S,3S,4S)-2-CARBOXY-4-[(1Z,3E,5R)-5-CARBOXY-1-MET...)copy SMILEScopy InChI
Affinity DataKi:  1.5nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM50002369((2S-(2alpha,3beta,4beta))-2-carboxy-4-(1-methyleth...)copy SMILEScopy InChI
Affinity DataKi:  1.80nMMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 3A(Mus musculus (house mouse))
Medical Research Council Centre

Curated by PDSP Ki Database
LigandPNGBDBM50241143((MDL 72222)3,5-Dichloro-benzoic acid 8-methyl-8-az...)copy SMILEScopy InChI
Affinity DataKi:  13nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9GR6PubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM85740(Dysiherbaine)copy SMILEScopy InChI
Affinity DataKi:  26nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM17657((2S)-2-aminopentanedioic acid | (S)-Glu | D-Glutam...)copy SMILEScopy InChI
Affinity DataKi:  62nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM17657((2S)-2-aminopentanedioic acid | (S)-Glu | D-Glutam...)copy SMILEScopy InChI
Affinity DataKi:  62nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM17657((2S)-2-aminopentanedioic acid | (S)-Glu | D-Glutam...)copy SMILEScopy InChI
Affinity DataKi:  89nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM85740(Dysiherbaine)copy SMILEScopy InChI
Affinity DataKi:  153nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM50252103((2S,3S,4S)-2-CARBOXY-4-[(1Z,3E,5R)-5-CARBOXY-1-MET...)copy SMILEScopy InChI
Affinity DataKi:  927nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM50002343(2-Methylamino-succinic acid | CHEMBL275325 | NMDA)copy SMILEScopy InChI
Affinity DataKi:  3.90E+3nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetGlutamate receptor 3(RAT)
Kitasato University

Curated by PDSP Ki Database
LigandPNGBDBM85740(Dysiherbaine)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2M0440CPubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
ARIAD Pharmaceuticals, Inc.

Curated by ChEMBL
LigandPNGBDBM23222(Oxalamic acid | Oxamate | Oxamate, 3 | Oxamidic Ac...)copy SMILEScopy InChI
Affinity DataKi:  2.60E+4nMAssay Description:Inhibition of human LDH-AMore data for this Ligand-Target Pair
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12255(AZD0530 | CHEMBL217092 | Compound 33 | N-(5-chloro...)copy SMILEScopy InChI
Affinity DataIC50: 2.70nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12241(AZD0530 analogue 19 | N-(5-chloro-2H-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50322823((S)-N-(4-(3-chloro-4-fluorophenylamino)-7-(tetrahy...)copy SMILEScopy InChI
Affinity DataIC50: 3.5nMMore data for this Ligand-Target Pair
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12247(AZD0530 analogue 25 | N-(5-chloro-2H-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12250(AZD0530 analogue 28 | N-(5-Chloro-1,3-benzodioxol-...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12252(AZD0530 analogue 30 | N-(5-Chloro-1,3-benzodioxol-...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6204(Benzofuran deriv. 13 | N-(3-Chloro-1-benzofuran-7-...)copy SMILEScopy InChI
Affinity DataIC50: 4nMpH: 7.4 T: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6210(Benzodioxole deriv. 19 | N-(5-Chloro-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 4nMpH: 7.4 T: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6211(Benzodioxole deriv. 20 | N-(5-Bromo-1,3-benzodioxo...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6219(BMCL182776 Compound 1 | Chlorobenzodioxole deriv. ...)copy SMILEScopy InChI
Affinity DataIC50: 4nMT: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12231(AZD0530 analogue 9 | N-(2-chloro-5-methoxyphenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 4nMpH: 7.4 T: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12237(AZD0530 analogue 15 | N-(5-chloro-2H-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12243(AZD0530 analogue 21 | N-(2-chloro-5-methoxyphenyl)...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12253(AZD0530 analogue 31 | N-(5-chloro-2H-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6218(AZD0530 analogue 34 | Chlorobenzodioxole deriv. 27...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12259(AZD0530 analogue 37 | N-(5-chloro-2H-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM50174939(CHEMBL424664 | N-(3-chloro-6-methoxypyridin-2-yl)-...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibitory activity against c-Src kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765DWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM50174932(CHEMBL197287 | N-(2-chloro-5-methoxypyridin-3-yl)-...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibitory activity against c-Src kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765DWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6218(AZD0530 analogue 34 | Chlorobenzodioxole deriv. 27...)copy SMILEScopy InChI
Affinity DataIC50: 5nMT: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM50174934(CHEMBL424839 | N-(3-chloro-6-methoxypyridin-2-yl)-...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibitory activity against c-Src kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765DWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12238(AZD0530 analogue 16 | N-(5-chloro-2H-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12240(AZD0530 analogue 18 | N-(5-Chloro-1,3-benzodioxol-...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12251(AZD0530 analogue 29 | N-(5-chloro-2H-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM50174935(CHEMBL371688 | N-(3-chloro-6-methoxypyridin-2-yl)-...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibitory activity against c-Src kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765DWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM50174929(CHEMBL369899 | N-(2-chloro-5-methoxypyridin-3-yl)-...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibitory activity against c-Src kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765DWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM50174936(1-(4-(2-(4-(3-chloro-6-methoxypyrazin-2-ylamino)-5...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibitory activity against c-Src kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765DWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12246(AZD0530 analogue 24 | N-(5-Chloro-1,3-benzodioxol-...)copy SMILEScopy InChI
Affinity DataIC50: 9.5nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM50174933(1-(4-(2-(4-(3-chloro-6-methoxypyridin-2-ylamino)-5...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibitory activity against c-Src kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765DWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM12229(AZD0530 analogue 7 | CHEMBL200217 | N-(2-Chloro-5-...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibitory activity against c-Src kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2765DWCPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6198(AZD0530 analogue 35 | M475271 | Methoxy Aniline 7 ...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67F5XPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6196(Methoxy Aniline 5 | N-(2-Chloro-5-methoxyphenyl)-6...)copy SMILEScopy InChI
Affinity DataIC50: 10nMpH: 7.4 T: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6198(AZD0530 analogue 35 | M475271 | Methoxy Aniline 7 ...)copy SMILEScopy InChI
Affinity DataIC50: 10nMpH: 7.4 T: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6200(Benzofuran deriv. 9 | N-(5-Chloro-1-benzofuran-4-y...)copy SMILEScopy InChI
Affinity DataIC50: 10nMpH: 7.4 T: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6202(Benzofuran deriv. 11 | N-(6-Chloro-1-benzofuran-7-...)copy SMILEScopy InChI
Affinity DataIC50: 10nMpH: 7.4 T: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6216(Benzodioxole deriv. 25 | N-(5-Chloro-1,3-benzodiox...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
AstraZeneca

LigandPNGBDBM6220(4-[({4-[(5-chloro-2H-1,3-benzodioxol-4-yl)amino]-6...)copy SMILEScopy InChI
Affinity DataIC50: 10nMT: 2°CAssay Description:This assay determines the ability of test compounds to inhibit Src kinase activity that catalyzes the transfer of the terminal phosphate to the immob...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930RCGPubMed
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