Compile Data Set for Download or QSAR
maximum 50k data
Found 16 with Last Name = 'wiech' and Initial = 'nl'
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Notre Dame

Curated by ChEMBL
LigandPNGBDBM50148757(2-[3-(2-Hydroxycarbamoyl-vinyl)-phenyl]-N,N'-diphe...)
Affinity DataIC50:  1nMAssay Description:Inhibitory activity against human Histone deacetylase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Notre Dame

Curated by ChEMBL
LigandPNGBDBM50148758(2-(Quinolin-6-ylcarbamoyl)-octanedioic acid 8-hydr...)
Affinity DataIC50:  1nMAssay Description:Inhibitory activity against human Histone deacetylase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Notre Dame

Curated by ChEMBL
LigandPNGBDBM50148759(CHEMBL323869 | [6-Hydroxycarbamoyl-1-(quinolin-8-y...)
Affinity DataIC50:  2.5nMAssay Description:Inhibitory activity against human Histone deacetylase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM29568(CHEMBL2 | PRAZOSIN | PRAZOSIN HYDROCHLORIDE | [3H]...)
Affinity DataIC50:  8nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A/Alpha-1B/Alpha-1D adrenergic receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50225742(CHEMBL537973)
Affinity DataIC50:  8nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A/Alpha-1B/Alpha-1D adrenergic receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50225741(CHEMBL15359)
Affinity DataIC50:  45nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A/Alpha-1B/Alpha-1D adrenergic receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50225740(CHEMBL15201)
Affinity DataIC50:  55nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A/Alpha-1B/Alpha-1D adrenergic receptor(Rattus norvegicus (rat))
TBA

Curated by ChEMBL
LigandPNGBDBM50225743(CHEMBL14987)
Affinity DataIC50:  90nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2b(Zea mays)
University Of Notre Dame

Curated by ChEMBL
LigandPNGBDBM50135752((2E)-N-hydroxy-3-[1-methyl-4-(phenylacetyl)-1H-pyr...)
Affinity DataIC50:  100nMAssay Description:Inhibitory activity against maize Histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50225741(CHEMBL15359)
Affinity DataIC50:  100nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Notre Dame

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  200nMAssay Description:Inhibitory activity against human Histone deacetylase 1More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Mus musculus (Mouse))
University Of Notre Dame

Curated by ChEMBL
LigandPNGBDBM50135752((2E)-N-hydroxy-3-[1-methyl-4-(phenylacetyl)-1H-pyr...)
Affinity DataIC50:  513nMAssay Description:Inhibitory activity against mouse Histone deacetylase 1 (HDAC1)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50225740(CHEMBL15201)
Affinity DataIC50:  600nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50225742(CHEMBL537973)
Affinity DataIC50:  800nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50225743(CHEMBL14987)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM29568(CHEMBL2 | PRAZOSIN | PRAZOSIN HYDROCHLORIDE | [3H]...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed