Compile Data Set for Download or QSAR
Found 513 with Last Name = 'fruttero' and Initial = 'r'
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131891(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  0.0940nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1A adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131889(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  0.160nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1A adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50057465(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  0.340nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1A adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131890(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  0.730nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1A adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131891(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  1.20nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1B adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131888(4-[2-(4-{3-[(3-Methyl-4-oxo-2-phenyl-4H-chromene-8...)
Affinity DataKi:  1.20nMAssay Description:Inhibition of [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor serotonergic receptor in human HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1D adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50057465(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  1.5nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1D adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131889(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  1.60nMAssay Description:Inhibition of [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor serotonergic receptor in human HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131888(4-[2-(4-{3-[(3-Methyl-4-oxo-2-phenyl-4H-chromene-8...)
Affinity DataKi:  1.80nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1A adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131890(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  2.20nMAssay Description:Inhibition of [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor serotonergic receptor in human HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050906(CHEMBL3309854)
Affinity DataKi:  2.90nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050905(CHEMBL3309853)
Affinity DataKi:  3.10nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1D adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131891(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  3.5nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1D adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050921(CHEMBL3309370)
Affinity DataKi:  3.80nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050920(CHEMBL3309369)
Affinity DataKi:  3.90nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50057465(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  3.90nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1B adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051028(CHEMBL3309359)
Affinity DataKi:  3.90nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1D adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131890(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  3.90nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1D adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050959(CHEMBL3309354)
Affinity DataKi:  4.20nMAssay Description:Inhibition of human CA2 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1D adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131889(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  4.20nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1D adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131889(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  4.70nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1B adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050958(CHEMBL3309353)
Affinity DataKi:  4.70nMAssay Description:Inhibition of human CA2 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051027(CHEMBL3309358)
Affinity DataKi:  4.80nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051029(CHEMBL3309360)
Affinity DataKi:  5.10nMAssay Description:Inhibition of human CA2 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051028(CHEMBL3309359)
Affinity DataKi:  5.30nMAssay Description:Inhibition of human CA2 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051027(CHEMBL3309358)
Affinity DataKi:  5.5nMAssay Description:Inhibition of human CA2 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050903(CHEMBL3309377)
Affinity DataKi:  5.60nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM10880(AZA | AZA2 | AZM acetazolamide | Acerazolamide, AA...)
Affinity DataKi:  5.70nMAssay Description:Inhibition of human CA12 by stopped-flow assayMore data for this Ligand-Target Pair
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051029(CHEMBL3309360)
Affinity DataKi:  5.80nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051025(CHEMBL3309356)
Affinity DataKi:  5.80nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050904(CHEMBL3309378)
Affinity DataKi:  5.90nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50057465(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  5.90nMAssay Description:Inhibition of [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor serotonergic receptor in human HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051026(CHEMBL3309357)
Affinity DataKi:  5.90nMAssay Description:Inhibition of human CA2 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050907(CHEMBL3309352)
Affinity DataKi:  5.90nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050923(CHEMBL3309372)
Affinity DataKi:  6nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050914(CHEMBL3309367)
Affinity DataKi:  6.10nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050922(CHEMBL3309371)
Affinity DataKi:  6.20nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051030(CHEMBL3309361)
Affinity DataKi:  6.30nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051030(CHEMBL3309361)
Affinity DataKi:  6.30nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050918(CHEMBL3309368)
Affinity DataKi:  6.30nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050963(CHEMBL3309355)
Affinity DataKi:  6.30nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050906(CHEMBL3309854)
Affinity DataKi:  6.40nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051025(CHEMBL3309356)
Affinity DataKi:  6.40nMAssay Description:Inhibition of human CA2 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050908(CHEMBL3309362)
Affinity DataKi:  6.5nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050959(CHEMBL3309354)
Affinity DataKi:  6.5nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Università degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50131890(3-Methyl-4-oxo-2-phenyl-4H-chromene-8-carboxylic a...)
Affinity DataKi:  6.5nMAssay Description:Inhibition of [3H]-prazosin binding to cloned human Alpha-1B adrenergic receptor in CHO-cells (chinese hamster ovary cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051026(CHEMBL3309357)
Affinity DataKi:  6.60nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50051026(CHEMBL3309357)
Affinity DataKi:  6.60nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 9(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50324356(3-phenyl-4-sulfamoyl-1,2,5-oxadiazole 2-oxide | CH...)
Affinity DataKi:  7.10nMAssay Description:Inhibition of human CA9 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 12(Homo sapiens (Human))
Universit£ degli Studi di Torino

Curated by ChEMBL
LigandPNGBDBM50050910(CHEMBL3309364)
Affinity DataKi:  7.10nMAssay Description:Inhibition of human CA12 by CO2 hydration activity based stopped flow assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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