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Found 679 with Last Name = 'durdagi' and Initial = 's'
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093582(CHEMBL3585782)
Affinity DataKi:  0.00500nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 1 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093587(CHEMBL3585777)
Affinity DataKi:  0.00500nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 2 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093588(CHEMBL3585776)
Affinity DataKi:  0.00500nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 2 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093589(CHEMBL3585775)
Affinity DataKi:  0.00600nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 2 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093581(CHEMBL3585783)
Affinity DataKi:  0.00600nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093583(CHEMBL3585781)
Affinity DataKi:  0.00600nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093597(CHEMBL3585784)
Affinity DataKi:  0.00800nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093585(CHEMBL3585779)
Affinity DataKi:  0.0110nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 1 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093586(CHEMBL3585778)
Affinity DataKi:  0.0230nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 2 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093584(CHEMBL3585780)
Affinity DataKi:  0.0380nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093585(CHEMBL3585779)
Affinity DataKi:  0.0460nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093587(CHEMBL3585777)
Affinity DataKi:  0.0480nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093586(CHEMBL3585778)
Affinity DataKi:  0.0490nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 2 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093589(CHEMBL3585775)
Affinity DataKi:  0.0600nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 2 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093587(CHEMBL3585777)
Affinity DataKi:  0.0890nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 2 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093585(CHEMBL3585779)
Affinity DataKi:  0.105nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 1 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093588(CHEMBL3585776)
Affinity DataKi:  0.127nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093589(CHEMBL3585775)
Affinity DataKi:  0.127nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093597(CHEMBL3585784)
Affinity DataKi:  0.137nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093586(CHEMBL3585778)
Affinity DataKi:  0.140nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093588(CHEMBL3585776)
Affinity DataKi:  0.156nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093584(CHEMBL3585780)
Affinity DataKi:  0.193nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50067742(7-((6aR,10aR)-1-Hydroxy-6,6,9-trimethyl-6a,7,10,10...)
Affinity DataKi:  0.200nMAssay Description:Binding affinity to CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50130624((6aR,10aR)-3-(2-hexyl-1,3-dioxolan-2-yl)-6,6,9-tri...)
Affinity DataKi:  0.220nMAssay Description:Binding affinity to CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50213605((6aR,10aR)-3-(2-cycloheptylpropan-2-yl)-6,6,9-trim...)
Affinity DataKi:  0.220nMAssay Description:Binding affinity to CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093584(CHEMBL3585780)
Affinity DataKi:  0.275nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50121425((6aR,10aR)-3-(2,2-Dichloro-1-hexyl-cyclopropyl)-6,...)
Affinity DataKi:  0.290nMAssay Description:Binding affinity to CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50063885((-)-2-(6a,7,10,10a-tetrahydro-6,6,9-trimethyl-1-hy...)
Affinity DataKi:  0.320nMAssay Description:Binding affinity to CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50063885((-)-2-(6a,7,10,10a-tetrahydro-6,6,9-trimethyl-1-hy...)
Affinity DataKi:  0.320nMAssay Description:Binding affinity to CB1 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50063885((-)-2-(6a,7,10,10a-tetrahydro-6,6,9-trimethyl-1-hy...)
Affinity DataKi:  0.324nMAssay Description:Binding affinity at CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50213607((6aR,10aR)-3-(2-cyclopentylpropan-2-yl)-6,6,9-trim...)
Affinity DataKi:  0.340nMAssay Description:Binding affinity to CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093581(CHEMBL3585783)
Affinity DataKi:  0.384nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50213607((6aR,10aR)-3-(2-cyclopentylpropan-2-yl)-6,6,9-trim...)
Affinity DataKi:  0.390nMAssay Description:Binding affinity to CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50213599((6aR,10aR)-3-(6-bromo-2-methylhexan-2-yl)-6,6,9-tr...)
Affinity DataKi:  0.430nMAssay Description:Binding affinity to CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50063884((6aR,10aR)-3-(1-Hexyl-cyclopropyl)-6,6,9-trimethyl...)
Affinity DataKi:  0.437nMAssay Description:Binding affinity at CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50063884((6aR,10aR)-3-(1-Hexyl-cyclopropyl)-6,6,9-trimethyl...)
Affinity DataKi:  0.440nMAssay Description:Binding affinity to CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50130623((6aR,10aR)-3-(1-hexylcyclopentyl)-6,6,9-trimethyl-...)
Affinity DataKi:  0.447nMAssay Description:Binding affinity at CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50161477(CHEMBL3785269)
Affinity DataKi:  0.450nMAssay Description:Inhibition of AChE (unknown origin) using acetylcholine iodate as substrate preincubated for 10 mins followed by substrate addition by Lineweaver-Bur...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50130623((6aR,10aR)-3-(1-hexylcyclopentyl)-6,6,9-trimethyl-...)
Affinity DataKi:  0.450nMAssay Description:Binding affinity to CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 2(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093582(CHEMBL3585782)
Affinity DataKi:  0.454nMAssay Description:Inhibition of acetylcholinesterase (unknown origin) assessed as AChI hydrolysis using AChI and DTNB as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093583(CHEMBL3585781)
Affinity DataKi:  0.479nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 1 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50067735((6aR,10aR)-3-(1,1-Dimethyl-heptyl)-6,6,9-trimethyl...)
Affinity DataKi:  0.490nMAssay Description:Binding affinity to CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50063885((-)-2-(6a,7,10,10a-tetrahydro-6,6,9-trimethyl-1-hy...)
Affinity DataKi:  0.520nMAssay Description:Binding affinity to CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50063885((-)-2-(6a,7,10,10a-tetrahydro-6,6,9-trimethyl-1-hy...)
Affinity DataKi:  0.520nMAssay Description:Binding affinity to CB2 receptor (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50130624((6aR,10aR)-3-(2-hexyl-1,3-dioxolan-2-yl)-6,6,9-tri...)
Affinity DataKi:  0.520nMAssay Description:Binding affinity to CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50130624((6aR,10aR)-3-(2-hexyl-1,3-dioxolan-2-yl)-6,6,9-tri...)
Affinity DataKi:  0.525nMAssay Description:Binding affinity at CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093581(CHEMBL3585783)
Affinity DataKi:  0.565nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 1 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50133544((6aR,10aR)-3-(1-Cyclohexyl-1-methyl-ethyl)-6,6,9-t...)
Affinity DataKi:  0.570nMAssay Description:Binding affinity to CB1 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
The National Hellenic Research Foundation

Curated by ChEMBL
LigandPNGBDBM50133544((6aR,10aR)-3-(1-Cyclohexyl-1-methyl-ethyl)-6,6,9-t...)
Affinity DataKi:  0.650nMAssay Description:Binding affinity to CB2 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCarbonic anhydrase 1(Homo sapiens (Human))
Agriibrahim£E£En University

Curated by ChEMBL
LigandPNGBDBM50093582(CHEMBL3585782)
Affinity DataKi:  0.657nMAssay Description:Inhibition of esterase activity of carbonic anhydrase 1 in human erythrocytes using PNF as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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