Compile Data Set for Download or QSAR
Found 30 with Last Name = 'berger' and Initial = 'y'
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159366((2S,4R)-4-Acetylsulfanyl-2-(2,4,5-trifluoro-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 6.90nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159365((3R,5S)-5-{[(2,5-difluorobenzyl)amino]methyl}-1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 10.4nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50098118((2S,4R)-4-Mercapto-2-(2,4,5-trifluoro-benzyloxymet...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159364(CHEMBL192441 | isopropyl (2S,4R)-2-{[(2,5-difluoro...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159367((2S,4R)-4-Benzoylsulfanyl-2-(2,4,5-trifluoro-benzy...)copy SMILEScopy InChI
Affinity DataIC50: 49.7nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159368((4R)-N'-methyl-N'-[(4-methylbenzene)sulfonyl]-1-(n...)copy SMILEScopy InChI
Affinity DataIC50: 61.3nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50098118((2S,4R)-4-Mercapto-2-(2,4,5-trifluoro-benzyloxymet...)copy SMILEScopy InChI
Affinity DataIC50: 67nMAssay Description:Inhibitory concentration against human ECE-1 expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159365((3R,5S)-5-{[(2,5-difluorobenzyl)amino]methyl}-1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 72.9nMAssay Description:Inhibitory concentration against human ECE-1 expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159366((2S,4R)-4-Acetylsulfanyl-2-(2,4,5-trifluoro-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 76.5nMAssay Description:Inhibitory concentration against human ECE-1 expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159363(CHEMBL177000 | methyl 2-(2-{N-methyl-1-[(4R)-1-(na...)copy SMILEScopy InChI
Affinity DataIC50: 80.8nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159367((2S,4R)-4-Benzoylsulfanyl-2-(2,4,5-trifluoro-benzy...)copy SMILEScopy InChI
Affinity DataIC50: 481nMAssay Description:Inhibitory concentration against human ECE-1 expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50251742((3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydro...)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159364(CHEMBL192441 | isopropyl (2S,4R)-2-{[(2,5-difluoro...)copy SMILEScopy InChI
Affinity DataIC50: 1.09E+3nMAssay Description:Inhibitory concentration against human ECE-1 expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159368((4R)-N'-methyl-N'-[(4-methylbenzene)sulfonyl]-1-(n...)copy SMILEScopy InChI
Affinity DataIC50: 2.53E+3nMAssay Description:Inhibitory concentration against human ECE-1 expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159363(CHEMBL177000 | methyl 2-(2-{N-methyl-1-[(4R)-1-(na...)copy SMILEScopy InChI
Affinity DataIC50: 1.09E+4nMAssay Description:Inhibitory concentration against human ECE-1 expressed in MDCK cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50098118((2S,4R)-4-Mercapto-2-(2,4,5-trifluoro-benzyloxymet...)copy SMILEScopy InChI
Affinity DataIC50: 1.34E+4nMAssay Description:Inhibitory concentration against human angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159368((4R)-N'-methyl-N'-[(4-methylbenzene)sulfonyl]-1-(n...)copy SMILEScopy InChI
Affinity DataIC50: 1.46E+4nMAssay Description:Inhibitory concentration against human angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159369(CGS-31,4447 | CHEMBL415967 | {1-[(S)-2-Biphenyl-4-...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory concentration against human ECE-1 by RIAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159365((3R,5S)-5-{[(2,5-difluorobenzyl)amino]methyl}-1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 3.15E+4nMAssay Description:Inhibitory concentration against human angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159363(CHEMBL177000 | methyl 2-(2-{N-methyl-1-[(4R)-1-(na...)copy SMILEScopy InChI
Affinity DataIC50: 3.66E+4nMAssay Description:Inhibitory concentration against human angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetNeprilysin(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159368((4R)-N'-methyl-N'-[(4-methylbenzene)sulfonyl]-1-(n...)copy SMILEScopy InChI
Affinity DataIC50: 3.92E+4nMAssay Description:Inhibitory concentration against NeprilysinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetNeprilysin(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159363(CHEMBL177000 | methyl 2-(2-{N-methyl-1-[(4R)-1-(na...)copy SMILEScopy InChI
Affinity DataIC50: 8.19E+4nMAssay Description:Inhibitory concentration against NeprilysinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetNeprilysin(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159365((3R,5S)-5-{[(2,5-difluorobenzyl)amino]methyl}-1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against NeprilysinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetNeprilysin(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159364(CHEMBL192441 | isopropyl (2S,4R)-2-{[(2,5-difluoro...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against NeprilysinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetNeprilysin(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159366((2S,4R)-4-Acetylsulfanyl-2-(2,4,5-trifluoro-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against NeprilysinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetNeprilysin(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159367((2S,4R)-4-Benzoylsulfanyl-2-(2,4,5-trifluoro-benzy...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against NeprilysinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetNeprilysin(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50098118((2S,4R)-4-Mercapto-2-(2,4,5-trifluoro-benzyloxymet...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against NeprilysinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159367((2S,4R)-4-Benzoylsulfanyl-2-(2,4,5-trifluoro-benzy...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against human angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159366((2S,4R)-4-Acetylsulfanyl-2-(2,4,5-trifluoro-benzyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against human angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
University Institute of Pathology

Curated by ChEMBL
LigandPNGBDBM50159364(CHEMBL192441 | isopropyl (2S,4R)-2-{[(2,5-difluoro...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against human angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VM4D1HPubMed