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Found 264 with Last Name = 'turcaud' and Initial = 's'
TargetNeprilysin(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407297(CHEMBL2052008)
Affinity DataKi:  0.700nMAssay Description:In vivo inhibitory potency against neutral endopeptidase by displacement of [3H]-HACBOGly binding in mouse kidneyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407297(CHEMBL2052008)
Affinity DataKi:  0.700nMAssay Description:In vivo inhibitory potency against neutral endopeptidase by displacement of [3H]-HACBOGly binding in mouse kidneyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407299(CHEMBL2052007)
Affinity DataKi:  1.60nMAssay Description:In vivo inhibitory potency against neutral endopeptidase by displacement of [3H]-HACBOGly binding in mouse kidneyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407299(CHEMBL2052007)
Affinity DataKi:  1.60nMAssay Description:In vivo inhibitory potency against neutral endopeptidase by displacement of [3H]-HACBOGly binding in mouse kidneyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Mus musculus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407299(CHEMBL2052007)
Affinity DataKi:  1.90nMAssay Description:Inhibitory potency against angiotensin converting enzyme by displacement of [3H]-trandolaprilate binding in mouse lungMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Mus musculus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407299(CHEMBL2052007)
Affinity DataKi:  1.90nMAssay Description:Inhibitory potency against angiotensin converting enzyme by displacement of [3H]-trandolaprilate binding in mouse lungMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407298(CHEMBL2051772)
Affinity DataKi:  5.30nMAssay Description:In vivo inhibitory potency against neutral endopeptidase by displacement of [3H]-HACBOGly binding in mouse kidneyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Mus musculus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407298(CHEMBL2051772)
Affinity DataKi:  10nMAssay Description:Inhibitory potency against angiotensin converting enzyme by displacement of [3H]-trandolaprilate binding in mouse lungMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Mus musculus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407297(CHEMBL2052008)
Affinity DataKi:  16nMAssay Description:Inhibitory potency against angiotensin converting enzyme by displacement of [3H]-trandolaprilate binding in mouse lungMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Mus musculus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50407297(CHEMBL2052008)
Affinity DataKi:  80nMAssay Description:Inhibitory potency against angiotensin converting enzyme by displacement of [3H]-trandolaprilate binding in mouse lungMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073671((1S,2R)-2-[1-[1-Benzylcarbamoyl-2-(1H-imidazol-4-y...)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073669((S)-1-{(R)-[(S)-1-[(S)-1-Benzylcarbamoyl-2-(3H-imi...)
Affinity DataKi:  3.90E+3nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073670((1R,2S)-2-[1-[1-Benzylcarbamoyl-2-(1H-imidazol-4-y...)
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073668((S)-1-{(R)-[(S)-1-[(S)-1-Carboxy-2-(3H-imidazol-4-...)
Affinity DataKi:  5.00E+3nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073678((1R,2R)-2-[1-[1-Benzylcarbamoyl-2-(1H-imidazol-4-y...)
Affinity DataKi:  6.00E+3nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073679((S)-1-{(S)-[(S)-1-[(S)-1-Benzylcarbamoyl-2-(3H-imi...)
Affinity DataKi:  6.80E+3nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073675((1S,2S)-2-[1-[1-Benzylcarbamoyl-2-(1H-imidazol-4-y...)
Affinity DataKi:  9.60E+3nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073674((S)-1-{(S)-[(S)-1-[(S)-1-Carboxy-2-(3H-imidazol-4-...)
Affinity DataKi:  1.50E+4nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073680(2-Mercapto-1-(3-sulfamoyl-phenyl)-ethyl-ammonium)
Affinity DataKi:  3.50E+4nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073673(N-[(2SR,3S)-3-Amino-5-carbamoyl-2-sulfanylpentanoy...)
Affinity DataKi:  8.00E+4nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073677(N-[(2SR,3S)-3-Amino-5-carbamoyl-2-sulfanylpentanoy...)
Affinity DataKi:  9.00E+4nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073676(N-[(2SR,3S)-3-Amino-5-carbamoyl-2-sulfanylpentanoy...)
Affinity DataKi:  1.00E+5nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073667(N-[(2SR,3S)-3-Amino-5-carbamoyl-2-sulfanylpentanoy...)
Affinity DataKi:  1.00E+5nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073666((R)-1-Mercaptomethyl-3-sulfamoyl-propyl-ammonium)
Affinity DataKi:  1.00E+5nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTetanus toxin(Clostridium tetani)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50073672((R)-3-Carbamoyl-1-mercaptomethyl-propyl-ammonium)
Affinity DataKi:  2.50E+5nMAssay Description:Inhibition of tetanus neurotoxin (TeNt)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050127((S)-3-(4-Hydroxy-phenyl)-2-[(2S,3R)-2-((S)-2-merca...)
Affinity DataIC50:  0.260nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050151(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50:  0.300nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050149(1-[(S)-2-((S)-2-Mercapto-4-phenyl-butyrylamino)-pr...)
Affinity DataIC50:  0.350nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050150(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50:  0.400nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051796((2S,5R)-5-(2-Hydroxy-phenyl)-1-{2-[(S)-2-mercapto-...)
Affinity DataIC50:  0.420nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051798((2S,5R)-5-(4-Hydroxy-phenyl)-1-{2-[(S)-3-(4-hydrox...)
Affinity DataIC50:  0.460nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051784((2S,5R)-5-(2-Hydroxy-phenyl)-1-[2-((S)-2-mercapto-...)
Affinity DataIC50:  0.5nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051785((2S,5R)-1-[2-((S)-2-Mercapto-3-phenyl-propionylami...)
Affinity DataIC50:  0.550nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050156((S)-1-[(S)-2-((2S,3S)-2-Mercapto-3-methyl-pentanoy...)
Affinity DataIC50:  0.580nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051780((2S,5R)-5-(2-Hydroxy-phenyl)-1-{2-[(S)-3-(4-hydrox...)
Affinity DataIC50:  0.600nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051791((2S,5R)-5-(3-Hydroxy-phenyl)-1-{2-[(S)-3-(4-hydrox...)
Affinity DataIC50:  0.700nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050144(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50:  0.850nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051803((2S,5R)-1-{2-[3-(4-Chloro-phenyl)-2-mercapto-propi...)
Affinity DataIC50:  0.900nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051784((2S,5R)-5-(2-Hydroxy-phenyl)-1-[2-((S)-2-mercapto-...)
Affinity DataIC50:  1nMAssay Description:In vitro inhibition of neutral endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050125(1-[(S)-2-((S)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50:  1.10nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051803((2S,5R)-1-{2-[3-(4-Chloro-phenyl)-2-mercapto-propi...)
Affinity DataIC50:  1.20nMAssay Description:In vitro inhibition of neutral endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50041071((2-Mercaptomethyl-3-phenyl-butyrylamino)-acetic ac...)
Affinity DataIC50:  1.30nMAssay Description:In vivo inhibitory potency against neutral endopeptidase by displacement of [3H]-HACBOGly binding in mouse kidneyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050158(1-[(S)-2-((R)-2-Mercapto-3-phenyl-propionylamino)-...)
Affinity DataIC50:  1.30nMAssay Description:Inhibitory activity was tested against neutral endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50002022((2-Benzyl-3-hydroxycarbamoyl-propionylamino)-aceti...)
Affinity DataIC50:  1.40nMAssay Description:Inhibitory potency against neutral endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050127((S)-3-(4-Hydroxy-phenyl)-2-[(2S,3R)-2-((S)-2-merca...)
Affinity DataIC50:  1.40nMAssay Description:Inhibitory activity was tested against neutral endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050162((S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-((S)-2-mercapto-...)
Affinity DataIC50:  1.5nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051800(1-{2-[(S)-3-(4-Hydroxy-phenyl)-2-mercapto-propiony...)
Affinity DataIC50:  1.5nMAssay Description:In vitro inhibition of neutral endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051790((2S,5R)-5-(3-Hydroxy-phenyl)-1-[2-((S)-2-mercapto-...)
Affinity DataIC50:  1.5nMAssay Description:In vitro inhibition of rat angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50051785((2S,5R)-1-[2-((S)-2-Mercapto-3-phenyl-propionylami...)
Affinity DataIC50:  1.60nMAssay Description:In vitro inhibition of neutral endopeptidaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50050148((S)-3-(4-Hydroxy-phenyl)-2-[(S)-2-((S)-2-mercapto-...)
Affinity DataIC50:  1.60nMAssay Description:Inhibitory activity against angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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