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Found 25 with Last Name = 'shadle' and Initial = 'jk'
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50084636(5-[1-[4-(4-Benzoyl-3-hydroxy-2-propyl-benzyloxy)-p...)
Affinity DataIC50:  210nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50080991(5-[1-[4-(4-Benzoyl-3-hydroxy-2-propyl-phenoxymethy...)
Affinity DataIC50:  340nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287763(5-[1-{4-[3-Hydroxy-4-(2-hydroxy-benzoyl)-2-propyl-...)
Affinity DataIC50:  620nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287749(5-[1-[4-(4-Acetyl-3-hydroxy-2-propyl-benzyloxy)-ph...)
Affinity DataIC50:  640nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287758(5-(2-Hydroxy-4-{4-[4-oxo-2-thioxo-thiazolidin-(5Z)...)
Affinity DataIC50:  690nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287743(5-[1-[4-(4-Benzoyl-phenoxymethyl)-phenyl]-meth-(Z)...)
Affinity DataIC50:  780nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287747(5-[1-[4-(4-Benzoyl-2-benzyl-3-hydroxy-phenoxymethy...)
Affinity DataIC50:  820nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50080991(5-[1-[4-(4-Benzoyl-3-hydroxy-2-propyl-phenoxymethy...)
Affinity DataIC50:  1.30E+3nMAssay Description:Compound was evaluated for the inhibition of cathepsin D at an enzyme level of 50 ng/mLMore data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287761(5-[1-[4-(4-Benzoyl-benzyloxy)-phenyl]-meth-(Z)-yli...)
Affinity DataIC50:  1.31E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287759(5-[1-{4-[3-Hydroxy-2-propyl-4-(pyridine-3-carbonyl...)
Affinity DataIC50:  1.46E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287742(5-[1-[4-(4-Acetyl-3-methoxy-2-propyl-benzyloxy)-ph...)
Affinity DataIC50:  1.86E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287750(5-[1-[4-(4-Acetyl-3-hydroxy-2-propyl-phenoxymethyl...)
Affinity DataIC50:  2.56E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287757(5-[1-[4-(3-Methoxy-2-propyl-phenoxymethyl)-phenyl]...)
Affinity DataIC50:  2.76E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287762(5-[1-[4-(3-Hydroxy-2-propyl-phenoxymethyl)-phenyl]...)
Affinity DataIC50:  2.94E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287752(Acetic acid 6-acetyl-3-{4-[4-oxo-2-thioxo-thiazoli...)
Affinity DataIC50:  2.98E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287745(5-[1-[4-(3-Hydroxy-4-propionyl-2-propyl-benzyloxy)...)
Affinity DataIC50:  3.69E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287760(2-Hydroxy-4-{4-[4-oxo-2-thioxo-thiazolidin-(5Z)-yl...)
Affinity DataIC50:  5.13E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287751(5-[1-[3-(4-Acetyl-3-hydroxy-2-propyl-benzyloxy)-ph...)
Affinity DataIC50:  6.64E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287753(5-[1-[4-(4-Benzoyl-3-hydroxy-phenoxymethyl)-phenyl...)
Affinity DataIC50:  7.20E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287748(5-[1-{4-[3-Hydroxy-2-propyl-4-(pyridine-4-carbonyl...)
Affinity DataIC50:  7.94E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287746(2-Hydroxy-4-{4-[4-oxo-2-thioxo-thiazolidin-(5Z)-yl...)
Affinity DataIC50:  9.74E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287755(5-[1-[4-(4-Acetyl-3-hydroxy-benzyloxy)-phenyl]-met...)
Affinity DataIC50:  1.41E+4nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287754(5-[1-[4-(4-Acetyl-2-ethyl-3-hydroxy-benzyloxy)-phe...)
Affinity DataIC50:  1.76E+4nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287744(Acetic acid 6-acetyl-3-{4-[4-oxo-2-thioxo-thiazoli...)
Affinity DataIC50:  3.30E+4nMAssay Description:Compound was evaluated for the inhibition of cathepsin D at concentration of 4.15 microg/mLMore data for this Ligand-Target Pair
In DepthDetails Article
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287756(5-[1-[4-(4-Acetyl-3-methoxy-2-propyl-phenoxymethyl...)
Affinity DataIC50:  4.84E+4nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article