Compile Data Set for Download or QSAR
Report error Found 55 Enz. Inhib. hit(s) with all data for entry = 50016273
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593777(CHEMBL5185868)
Affinity DataIC50: 0.800nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593778(CHEMBL5189408)
Affinity DataIC50: 2.80nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM8960(2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimethoxy-2...)
Affinity DataIC50: 17nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMedPDB3D3D Structure (crystal)
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50307083(4-nitrophenyl 4-(3-phenoxybenzyl)piperazine-1-carb...)
Affinity DataIC50: 19nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593779(CHEMBL5193520)
Affinity DataIC50: 42nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593781(CHEMBL5190969)
Affinity DataIC50: 90nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593768(CHEMBL5195980)
Affinity DataIC50: 103nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593767(CHEMBL5207120)
Affinity DataIC50: 122nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593773(CHEMBL5182803)
Affinity DataIC50: 135nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593780(CHEMBL5209013)
Affinity DataIC50: 136nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593785(CHEMBL5169781)
Affinity DataIC50: 189nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593784(CHEMBL5175715)
Affinity DataIC50: 300nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593780(CHEMBL5209013)
Affinity DataIC50: 503nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593769(CHEMBL5180014)
Affinity DataIC50: 509nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593771(CHEMBL5178350)
Affinity DataIC50: 595nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593776(CHEMBL5204532)
Affinity DataIC50: 735nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593770(CHEMBL5202267)
Affinity DataIC50: 767nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593774(CHEMBL5177371)
Affinity DataIC50: 880nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593783(CHEMBL5185234)
Affinity DataIC50: 900nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593776(CHEMBL5204532)
Affinity DataIC50: 969nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593782(CHEMBL5206245)
Affinity DataIC50: 993nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593770(CHEMBL5202267)
Affinity DataIC50: 1.02E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593772(CHEMBL5203325)
Affinity DataIC50: 1.27E+3nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593777(CHEMBL5185868)
Affinity DataIC50: 1.41E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593775(CHEMBL5175950)
Affinity DataIC50: 1.68E+3nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetAcetylcholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593766(CHEMBL5170984)
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of human AChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593785(CHEMBL5169781)
Affinity DataIC50: 2.15E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593771(CHEMBL5178350)
Affinity DataIC50: 2.22E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593781(CHEMBL5190969)
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593767(CHEMBL5207120)
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM8960(2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimethoxy-2...)
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593778(CHEMBL5189408)
Affinity DataIC50: 5.01E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593773(CHEMBL5182803)
Affinity DataIC50: 5.08E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593766(CHEMBL5170984)
Affinity DataIC50: 5.58E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetCholinesterase(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593775(CHEMBL5175950)
Affinity DataIC50: 5.61E+3nMAssay Description:Inhibition of human BuChE by Ellman's spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593783(CHEMBL5185234)
Affinity DataIC50: 1.68E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593775(CHEMBL5175950)
Affinity DataIC50: 2.09E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593772(CHEMBL5203325)
Affinity DataIC50: 2.19E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593767(CHEMBL5207120)
Affinity DataIC50: 2.33E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593766(CHEMBL5170984)
Affinity DataIC50: 2.33E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593782(CHEMBL5206245)
Affinity DataIC50: 2.36E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593773(CHEMBL5182803)
Affinity DataIC50: 2.38E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593768(CHEMBL5195980)
Affinity DataIC50: 2.81E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593769(CHEMBL5180014)
Affinity DataIC50: 2.85E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593771(CHEMBL5178350)
Affinity DataIC50: 2.86E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593770(CHEMBL5202267)
Affinity DataIC50: 3.82E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593774(CHEMBL5177371)
Affinity DataIC50: 4.08E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593781(CHEMBL5190969)
Affinity DataIC50: 4.08E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593777(CHEMBL5185868)
Affinity DataIC50: 4.16E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
TargetFatty-acid amide hydrolase 1(Human)
University of Bari Aldo Moro

Curated by ChEMBL
LigandPNGBDBM50593779(CHEMBL5193520)
Affinity DataIC50: 4.39E+4nMAssay Description:Inhibition of human recombinant FAAH using AMC-AA as substrate preincubated with enzyme for 10 mins followed by substrate addition for 2 hrs by fluor...More data for this Ligand-Target Pair
In DepthDetails
PubMed
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