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Found 81 with Last Name = 'sastry' and Initial = 'gn'
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM21173(1,3-dipropyl-8-cyclopentylxanthine | 8-cyclopentyl...)
Affinity DataKi:  0.5nMAssay Description:Displacement of [3H]CCPA from adenosine A1 receptor in rat brain cortical membrane after 90 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316843(2-Phenyl-4-(prop-2-yn-1-yloxy)-5,6,7,8-tetrahydro[...)
Affinity DataKi:  3nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316849(2-(4-Fluorobenzyl)-5,6-dimethyl-3-prop-2-yn-1-ylth...)
Affinity DataKi:  4nMAssay Description:Displacement of [3H]CCPA from adenosine A1 receptor in rat brain cortical membrane after 90 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316851(2-Phenyl-3-prop-2-yn-1-yl-3,5,6,7-tetrahydro-4H-cy...)
Affinity DataKi:  5nMAssay Description:Displacement of [3H]CCPA from adenosine A1 receptor in rat brain cortical membrane after 90 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316847(2,5,6-Trimethyl-3-prop-2-yn-1-ylthieno[2,3-d]pyrim...)
Affinity DataKi:  6nMAssay Description:Displacement of [3H]CCPA from adenosine A1 receptor in rat brain cortical membrane after 90 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316850(2-Methyl-3-prop-2-yn-1-yl-3,5,6,7-tetrahydro-4H-cy...)
Affinity DataKi:  6nMAssay Description:Displacement of [3H]CCPA from adenosine A1 receptor in rat brain cortical membrane after 90 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316845(2-Methyl-3-prop-2-yn-1-yl-5, 6, 7, 8-tetrahydro [1...)
Affinity DataKi:  7nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316846(2-(4-Fluorobenzyl)-3-prop-2-yn-1-yl-5,6,7,8-tetrah...)
Affinity DataKi:  14nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316850(2-Methyl-3-prop-2-yn-1-yl-3,5,6,7-tetrahydro-4H-cy...)
Affinity DataKi:  18nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316846(2-(4-Fluorobenzyl)-3-prop-2-yn-1-yl-5,6,7,8-tetrah...)
Affinity DataKi:  21nMAssay Description:Displacement of [3H]CCPA from adenosine A1 receptor in rat brain cortical membrane after 90 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316848(5,6-Dimethyl-2-phenyl-3-prop-2-yn-1-ylthieno[2, 3-...)
Affinity DataKi:  29nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM21173(1,3-dipropyl-8-cyclopentylxanthine | 8-cyclopentyl...)
Affinity DataKi:  157nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316847(2,5,6-Trimethyl-3-prop-2-yn-1-ylthieno[2,3-d]pyrim...)
Affinity DataKi:  3.79E+3nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316849(2-(4-Fluorobenzyl)-5,6-dimethyl-3-prop-2-yn-1-ylth...)
Affinity DataKi:  7.62E+3nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Institute Of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50316851(2-Phenyl-3-prop-2-yn-1-yl-3,5,6,7-tetrahydro-4H-cy...)
Affinity DataKi:  9.70E+3nMAssay Description:Displacement of [3H]MSX-2 from adenosine A2A receptor in rat brain striatal membrane after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099348(2-(2,4-Dimethyl-phenoxy)-4-[5-(4-fluoro-phenyl)-3-...)
Affinity DataIC50:  6nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099358(2-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imid...)
Affinity DataIC50:  6.60nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099373(2-(4-Ethyl-phenoxy)-4-[5-(4-fluoro-phenyl)-3-piper...)
Affinity DataIC50:  7.40nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099345(2-(2,5-Dimethyl-phenoxy)-4-[5-(4-fluoro-phenyl)-3-...)
Affinity DataIC50:  11nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099343(2-(2-Fluoro-phenoxy)-4-[5-(4-fluoro-phenyl)-3-pipe...)
Affinity DataIC50:  13nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099367(4-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imid...)
Affinity DataIC50:  14nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099349(2-(2,3-Dimethyl-phenoxy)-4-[5-(4-fluoro-phenyl)-3-...)
Affinity DataIC50:  15nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099342(4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imidazo...)
Affinity DataIC50:  15nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099374(4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imidazo...)
Affinity DataIC50:  19nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099352(4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imidazo...)
Affinity DataIC50:  19nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099341(4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imidazo...)
Affinity DataIC50:  20nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099347(2-(3,4-Dimethyl-phenoxy)-4-[5-(4-fluoro-phenyl)-3-...)
Affinity DataIC50:  22nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099338(2-(Benzo[1,3]dioxol-5-yloxy)-4-[5-(4-fluoro-phenyl...)
Affinity DataIC50:  23nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099334(4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imidazo...)
Affinity DataIC50:  25nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099353(2-(2,6-Dimethyl-phenoxy)-4-[5-(4-fluoro-phenyl)-3-...)
Affinity DataIC50:  34.3nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099333(2-(3,5-Dimethyl-phenoxy)-4-[5-(4-fluoro-phenyl)-3-...)
Affinity DataIC50:  41nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099365(4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imidazo...)
Affinity DataIC50:  41nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099329(3-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imid...)
Affinity DataIC50:  56nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099328(2-(Biphenyl-4-yloxy)-4-[5-(4-fluoro-phenyl)-3-pipe...)
Affinity DataIC50:  60nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099364(3-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imid...)
Affinity DataIC50:  75nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099340(2-(4-tert-Butyl-phenoxy)-4-[5-(4-fluoro-phenyl)-3-...)
Affinity DataIC50:  79nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099360(4-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imid...)
Affinity DataIC50:  82nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50345778(CHEMBL1784928 | ethyl 4-(4-(4-(4-fluorophenyl)-1-(...)
Affinity DataIC50:  85.4nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099350(4-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imid...)
Affinity DataIC50:  89.7nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099346(2-(3-Fluoro-phenoxy)-4-[5-(4-fluoro-phenyl)-3-pipe...)
Affinity DataIC50:  95nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099366(2-(4-Chloro-phenoxy)-4-[5-(4-fluoro-phenyl)-3-pipe...)
Affinity DataIC50:  114nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099332((4-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imi...)
Affinity DataIC50:  119nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099359(4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imidazo...)
Affinity DataIC50:  130nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099335(4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imidazo...)
Affinity DataIC50:  132nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50345779(2-(2-(4-(4-(4-fluorophenyl)-1-(piperidin-4-yl)-1H-...)
Affinity DataIC50:  134nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50345780(3-(2-(4-(4-(4-fluorophenyl)-1-(piperidin-4-yl)-1H-...)
Affinity DataIC50:  151nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099357(2-(3,4-Dichloro-phenoxy)-4-[5-(4-fluoro-phenyl)-3-...)
Affinity DataIC50:  165nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099356(4-(4-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-i...)
Affinity DataIC50:  174nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099337(4-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imid...)
Affinity DataIC50:  177nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 14(Homo sapiens (Human))
University College Of Pharmaceutical Sciences

Curated by ChEMBL
LigandPNGBDBM50099371(3-{4-[5-(4-Fluoro-phenyl)-3-piperidin-4-yl-3H-imid...)
Affinity DataIC50:  191nMAssay Description:Inhibition of p38alphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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