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Found 444 with Last Name = 'albert' and Initial = 'e'
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM21653((2S)-2-[(2R)-2-[(1R)-2,3-dihydro-1H-inden-1-yl]-3-...)
Affinity DataKi:  0.700nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002726(CHEMBL2371933)
Affinity DataKi:  0.910nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002718(CHEMBL385281)
Affinity DataKi:  1.10nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50320463(CHEMBL218994 | D[CFWKYC]V | H-Asp-Cys-Phe-Trp-Lys-...)
Affinity DataKi:  1.20nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTryptase beta-2(Homo sapiens (Human))
Aventis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50156461(3-[4-(5-Aminomethyl-2-fluoro-phenyl)-piperidine-1-...)
Affinity DataKi:  1.30nMAssay Description:Inhibitory activity against human mast cell tryptase betaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115846((S)-3-(1H-Indol-3-yl)-2-[(R)-3-mercapto-2-((R)-5-m...)
Affinity DataKi:  1.30nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTryptase beta-2(Homo sapiens (Human))
Aventis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50156460(3-[4-(3-Aminomethyl-phenyl)-piperidine-1-carbonyl]...)
Affinity DataKi:  1.5nMAssay Description:Inhibitory activity against human mast cell tryptase betaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002725(CHEMBL374468)
Affinity DataKi:  1.60nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115843((2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-...)
Affinity DataKi:  1.80nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115842(2-(2-Indan-1-yl-3-mercapto-propionylamino)-3-(1H-i...)
Affinity DataKi:  1.80nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNischarin(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50127591(2-(4,5-Dihydro-1H-imidazol-2-yl)-4,6-dimethyl-3,4-...)
Affinity DataKi:  2nMAssay Description:In vitro binding affinity determined against imidazoline receptor I-2 using rabbit kidney preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002728(CHEMBL218825)
Affinity DataKi:  2.20nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002723(CHEMBL265166)
Affinity DataKi:  2.40nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115850((S)-3-(1H-Indol-3-yl)-2-[(S)-3-mercapto-2-((R)-5-m...)
Affinity DataKi:  2.70nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002717(CHEMBL216712)
Affinity DataKi:  2.90nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002727(CHEMBL266651)
Affinity DataKi:  3nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115837(2-[2-(5-Cyano-indan-1-yl)-3-mercapto-propionylamin...)
Affinity DataKi:  3nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115840((S)-2-[(S)-2-(5-Bromo-indan-1-yl)-3-mercapto-propi...)
Affinity DataKi:  3.80nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115839(2-[2-(5-Hydroxy-indan-1-yl)-3-mercapto-propionylam...)
Affinity DataKi:  4nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115840((S)-2-[(S)-2-(5-Bromo-indan-1-yl)-3-mercapto-propi...)
Affinity DataKi:  4.10nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTryptase beta-2(Homo sapiens (Human))
Aventis Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50156457(CHEMBL186730 | [4-(5-Aminomethyl-2-fluoro-phenyl)-...)
Affinity DataKi:  4.30nMAssay Description:Inhibitory activity against human mast cell tryptase betaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115850((S)-3-(1H-Indol-3-yl)-2-[(S)-3-mercapto-2-((R)-5-m...)
Affinity DataKi:  4.60nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115845(2-[2-(5-Bromo-indan-1-yl)-3-mercapto-propionylamin...)
Affinity DataKi:  5nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115841(3-(1H-Indol-3-yl)-2-[3-mercapto-2-(5-methoxy-indan...)
Affinity DataKi:  5nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115849(3-(1H-Indol-3-yl)-2-[3-mercapto-2-(5-methylsulfany...)
Affinity DataKi:  6nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115839(2-[2-(5-Hydroxy-indan-1-yl)-3-mercapto-propionylam...)
Affinity DataKi:  7nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNischarin(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50127595(2-(4,5-Dihydro-1H-imidazol-2-yl)-4-methyl-3,4-dihy...)
Affinity DataKi:  7nMAssay Description:In vitro binding affinity determined against imidazoline receptor I-2 using rabbit kidney preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115836(3-(1H-Indol-3-yl)-2-[3-mercapto-2-(4-methoxy-indan...)
Affinity DataKi:  8nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115838(2-[2-(5-Ethoxy-indan-1-yl)-3-mercapto-propionylami...)
Affinity DataKi:  8nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002716(CHEMBL383996)
Affinity DataKi:  9.10nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115851((S)-2-[(S)-2-((S)-5-Bromo-indan-1-yl)-3-mercapto-p...)
Affinity DataKi:  9.40nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115846((S)-3-(1H-Indol-3-yl)-2-[(R)-3-mercapto-2-((R)-5-m...)
Affinity DataKi:  10nMAssay Description:In vitro inhibition of endothelin converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNischarin(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50127600(2-(4,5-Dihydro-1H-imidazol-2-yl)-2,3,5,6-tetrahydr...)
Affinity DataKi:  10nMAssay Description:In vitro binding affinity determined against imidazoline receptor I-2 using rabbit kidney preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrotensin-2 receptor(Homo sapiens (Human))
University Of Rouen

Curated by ChEMBL
LigandPNGBDBM50002719(CHEMBL412179)
Affinity DataKi:  10nMAssay Description:Displacement of [125I]human urotensin-2 from human GPR14 transfected in CHO cellsChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115835(3-(1H-Indol-3-yl)-2-[3-mercapto-2-(6-methoxy-indan...)
Affinity DataKi:  11nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115837(2-[2-(5-Cyano-indan-1-yl)-3-mercapto-propionylamin...)
Affinity DataKi:  11nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115841(3-(1H-Indol-3-yl)-2-[3-mercapto-2-(5-methoxy-indan...)
Affinity DataKi:  11nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115845(2-[2-(5-Bromo-indan-1-yl)-3-mercapto-propionylamin...)
Affinity DataKi:  12nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNischarin(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50127590(4-(4,5-Dihydro-1H-imidazol-2-yl)-3,4-dihydro-5-oxa...)
Affinity DataKi:  13nMAssay Description:In vitro binding affinity determined against imidazoline receptor I-1 from rabbit kidney preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNischarin(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50127590(4-(4,5-Dihydro-1H-imidazol-2-yl)-3,4-dihydro-5-oxa...)
Affinity DataKi:  13nMAssay Description:In vitro binding affinity determined against imidazoline receptor I-1 from rabbit kidney preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115847((2S)-2-[(2R)-2-[(1S)-5-bromo-2,3-dihydro-1H-inden-...)
Affinity DataKi:  13nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115834(3-(1H-Indol-3-yl)-2-[3-mercapto-2-(5-phenyl-indan-...)
Affinity DataKi:  14nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115849(3-(1H-Indol-3-yl)-2-[3-mercapto-2-(5-methylsulfany...)
Affinity DataKi:  14nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115852(2-[2-(5-Dimethylamino-indan-1-yl)-3-mercapto-propi...)
Affinity DataKi:  15nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115848((S)-3-(1H-Indol-3-yl)-2-[(R)-3-mercapto-2-((S)-5-m...)
Affinity DataKi:  15nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNeprilysin(Oryctolagus cuniculus (rabbit))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115836(3-(1H-Indol-3-yl)-2-[3-mercapto-2-(4-methoxy-indan...)
Affinity DataKi:  16nMAssay Description:In vitro inhibition of Neutral endopeptidase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNischarin(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50127572(2-(4,5-Dihydro-1H-imidazol-2-yl)-6-fluoro-4-methyl...)
Affinity DataKi:  17nMAssay Description:In vitro binding affinity determined against imidazoline receptor I-2 using rabbit kidney preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNischarin(Homo sapiens (Human))
Université

Curated by ChEMBL
LigandPNGBDBM50127573(2-(4,5-Dihydro-1H-imidazol-2-yl)-6-ethoxymethyl-4-...)
Affinity DataKi:  17nMAssay Description:In vitro binding affinity determined against imidazoline receptor I-2 using rabbit kidney preparationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115838(2-[2-(5-Ethoxy-indan-1-yl)-3-mercapto-propionylami...)
Affinity DataKi:  18nMAssay Description:In vitro inhibition of Angiotensin I converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEndothelin-converting enzyme 1(Homo sapiens (Human))
University Of Paris

Curated by ChEMBL
LigandPNGBDBM50115843((2S)-2-[(2R)-2-[(1R)-5-bromo-2,3-dihydro-1H-inden-...)
Affinity DataKi:  18nMAssay Description:In vitro inhibition of endothelin converting enzyme.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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