Compile Data Set for Download or QSAR
Found 228 with Last Name = 'meyners' and Initial = 'c'
TargetHistone deacetylase 7(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361254(CHEMBL1934896)copy SMILEScopy InChI
Affinity DataKi:  2.50E+3nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361254(CHEMBL1934896)copy SMILEScopy InChI
Affinity DataKi:  7.00E+3nMAssay Description:Inhibition of human HDAC1 using Boc-Lys(Ac)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by trypsi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361254(CHEMBL1934896)copy SMILEScopy InChI
Affinity DataKi:  8.40E+3nMAssay Description:Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361248(CHEMBL1934890)copy SMILEScopy InChI
Affinity DataKi:  1.30E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataKi:  1.40E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361254(CHEMBL1934896)copy SMILEScopy InChI
Affinity DataKi:  2.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235702(CHEMBL4104197)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC8 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235705(CHEMBL4093113)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361254(CHEMBL1934896)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361266(CHEMBL1934908)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361267(CHEMBL1934909)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361265(CHEMBL1934907)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361253(CHEMBL1934895)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235708(CHEMBL4079958)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235702(CHEMBL4104197)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235705(CHEMBL4093113)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235707(CHEMBL4095542)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361264(CHEMBL1934906)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361248(CHEMBL1934890)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235703(CHEMBL4066515)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235707(CHEMBL4095542)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361251(CHEMBL1934893)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361268(CHEMBL1934910)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361262(CHEMBL1934904)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361255(CHEMBL1934897)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361249(CHEMBL1934891)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235703(CHEMBL4066515)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235707(CHEMBL4095542)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235701(CHEMBL4098910)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361259(CHEMBL1934901)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity against human NMB receptor was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235701(CHEMBL4098910)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC1 using Boc-Lys(Ac)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by trypsi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235702(CHEMBL4104197)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC7 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361251(CHEMBL1934893)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235703(CHEMBL4066515)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235704(CHEMBL4066343)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235705(CHEMBL4093113)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235706(CHEMBL4080874)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC7 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235702(CHEMBL4104197)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235705(CHEMBL4093113)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC6 using Boc-Lys(Ac)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by trypsi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361260(CHEMBL1934902)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235704(CHEMBL4066343)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235703(CHEMBL4066515)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361259(CHEMBL1934901)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361260(CHEMBL1934902)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361258(CHEMBL1934900)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235703(CHEMBL4066515)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC7 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50361263(CHEMBL1934905)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235701(CHEMBL4098910)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University of Applied Sciences Darmstadt

Curated by ChEMBL
LigandPNGBDBM50235707(CHEMBL4095542)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC6 using Boc-Lys(Ac)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by trypsi...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD502HPubMed
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