Compile Data Set for Download or QSAR
Report error Found 81 Enz. Inhib. hit(s) with all data for entry = 50013309 Sort by
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128955(1H-Indole-2-carboxylic acid {(S)-1-[2-(4-isobutoxy...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128951(4-Ethyl-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethylc...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128962(N-{(S)-1-[2-(4-Cyclopentylmethoxy-phenylamino)-eth...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128957(1H-Indole-2-carboxylic acid {(S)-1-[2-(4-cyclopent...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128960(N-{(S)-1-[2-(4-Benzyloxy-phenylamino)-ethylcarbamo...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128964(N-{(S)-1-[2-(4-Isobutoxy-phenylamino)-ethylcarbamo...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128965(1H-Indole-2-carboxylic acid {(S)-1-[2-(4-cyclohexy...)
Affinity DataIC50: 4nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50113674(4-Methoxy-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethy...)
Affinity DataIC50: 9nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128949(N-{(S)-1-[2-(4-Methoxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 30nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128951(4-Ethyl-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethylc...)
Affinity DataIC50: 30nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128950(1H-Indole-2-carboxylic acid {(S)-1-[2-(4-methoxy-p...)
Affinity DataIC50: 30nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM19545((2S)-N-{2-[(4-methoxyphenyl)amino]ethyl}-4-methyl-...)
Affinity DataIC50: 32nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128953({(S)-1-[2-(4-Isobutoxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 36nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128971({(S)-1-[2-(4-Cyclohexyloxy-phenylamino)-ethylcarba...)
Affinity DataIC50: 43nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128949(N-{(S)-1-[2-(4-Methoxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 44nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128954({(S)-1-[2-(4-Cyclopentylmethoxy-phenylamino)-ethyl...)
Affinity DataIC50: 49nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128961({(S)-1-[2-(4-Benzyloxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 54nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128952({(S)-1-[2-(4-Cyclopropylmethoxy-phenylamino)-ethyl...)
Affinity DataIC50: 69nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50113676({1-[2-(4-Methoxy-phenylamino)-ethylcarbamoyl]-3-me...)
Affinity DataIC50: 70nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM19545((2S)-N-{2-[(4-methoxyphenyl)amino]ethyl}-4-methyl-...)
Affinity DataIC50: 70nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128959({(S)-1-[2-(4-Cyclopentyloxy-phenylamino)-ethylcarb...)
Affinity DataIC50: 81nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128950(1H-Indole-2-carboxylic acid {(S)-1-[2-(4-methoxy-p...)
Affinity DataIC50: 90nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128969(3-Methoxy-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethy...)
Affinity DataIC50: 130nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128967(N-{(S)-1-[2-(4-Methoxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 150nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128968(((S)-3-Methyl-1-{2-[4-(pyridin-4-ylmethoxy)-phenyl...)
Affinity DataIC50: 152nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128950(1H-Indole-2-carboxylic acid {(S)-1-[2-(4-methoxy-p...)
Affinity DataIC50: 160nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128956(((S)-3-Methyl-1-{2-[4-(tetrahydro-pyran-4-yloxy)-p...)
Affinity DataIC50: 190nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128970({(S)-3-Methyl-1-[2-(4-phenoxy-phenylamino)-ethylca...)
Affinity DataIC50: 280nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128967(N-{(S)-1-[2-(4-Methoxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 320nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM19545((2S)-N-{2-[(4-methoxyphenyl)amino]ethyl}-4-methyl-...)
Affinity DataIC50: 372nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128969(3-Methoxy-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethy...)
Affinity DataIC50: 419nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128969(3-Methoxy-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethy...)
Affinity DataIC50: 470nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128964(N-{(S)-1-[2-(4-Isobutoxy-phenylamino)-ethylcarbamo...)
Affinity DataIC50: 480nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128962(N-{(S)-1-[2-(4-Cyclopentylmethoxy-phenylamino)-eth...)
Affinity DataIC50: 480nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128967(N-{(S)-1-[2-(4-Methoxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 490nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128964(N-{(S)-1-[2-(4-Isobutoxy-phenylamino)-ethylcarbamo...)
Affinity DataIC50: 580nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128962(N-{(S)-1-[2-(4-Cyclopentylmethoxy-phenylamino)-eth...)
Affinity DataIC50: 580nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128949(N-{(S)-1-[2-(4-Methoxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 580nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128951(4-Ethyl-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethylc...)
Affinity DataIC50: 660nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50113674(4-Methoxy-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethy...)
Affinity DataIC50: 800nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128972(((S)-1-{2-[4-(2-Imidazol-1-yl-ethoxy)-phenylamino]...)
Affinity DataIC50: 855nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128958(((S)-3-Methyl-1-{2-[4-(1-methyl-piperidin-4-yloxy)...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128963(((S)-1-{2-[4-(2-Dimethylamino-ethoxy)-phenylamino]...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin K(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128966(((S)-3-Methyl-1-{2-[4-(2-pyrrolidin-1-yl-ethoxy)-p...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin K activity using fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128954({(S)-1-[2-(4-Cyclopentylmethoxy-phenylamino)-ethyl...)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128971({(S)-1-[2-(4-Cyclohexyloxy-phenylamino)-ethylcarba...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128953({(S)-1-[2-(4-Isobutoxy-phenylamino)-ethylcarbamoyl...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProcathepsin L(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128960(N-{(S)-1-[2-(4-Benzyloxy-phenylamino)-ethylcarbamo...)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin L activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50113674(4-Methoxy-N-{(S)-1-[2-(4-methoxy-phenylamino)-ethy...)
Affinity DataIC50: 1.55E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCathepsin S(Human)
Novartis Pharma

Curated by ChEMBL
LigandPNGBDBM50128952({(S)-1-[2-(4-Cyclopropylmethoxy-phenylamino)-ethyl...)
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibitory activity against recombinant human cathepsin S activityMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
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