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Found 296 with Last Name = 'mishra' and Initial = 'n'
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341160(3-(anthracen-9-yl)-5-(3-nitrophenyl)-4,5-dihydro-1...)
Affinity DataKi:  0.310nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341160(3-(anthracen-9-yl)-5-(3-nitrophenyl)-4,5-dihydro-1...)
Affinity DataKi:  0.450nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341161(3-(anthracen-9-yl)-5-(4-methoxyphenyl)-4,5-dihydro...)
Affinity DataKi:  0.600nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341152(3-(anthracen-9-yl)-5-(4-nitrophenyl)-4,5-dihydro-1...)
Affinity DataKi:  1.15nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341161(3-(anthracen-9-yl)-5-(4-methoxyphenyl)-4,5-dihydro...)
Affinity DataKi:  1.70nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341154(3-(anthracen-9-yl)-5-(4-chlorophenyl)-4,5-dihydro-...)
Affinity DataKi:  1.80nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341154(3-(anthracen-9-yl)-5-(4-chlorophenyl)-4,5-dihydro-...)
Affinity DataKi:  2.10nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341152(3-(anthracen-9-yl)-5-(4-nitrophenyl)-4,5-dihydro-1...)
Affinity DataKi:  2.30nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341156(3-(anthracen-9-yl)-5-phenyl-4,5-dihydro-1H-pyrazol...)
Affinity DataKi:  3.43nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341155(3-(anthracen-9-yl)-5-p-tolyl-4,5-dihydro-1H-pyrazo...)
Affinity DataKi:  3.56nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341155(3-(anthracen-9-yl)-5-p-tolyl-4,5-dihydro-1H-pyrazo...)
Affinity DataKi:  3.80nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341156(3-(anthracen-9-yl)-5-phenyl-4,5-dihydro-1H-pyrazol...)
Affinity DataKi:  4.21nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341158(4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  4.77nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341158(4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  5.54nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341159(2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  5.75nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341157(2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  5.91nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341153(4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  6.75nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)
Affinity DataKi:  7.20nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425411(CHEMBL2312573)
Affinity DataKi:  7.20nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341157(2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  7.35nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341153(4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  7.51nMAssay Description:Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341159(2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  9.91nMAssay Description:Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341152(3-(anthracen-9-yl)-5-(4-nitrophenyl)-4,5-dihydro-1...)
Affinity DataKi:  17.1nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341152(3-(anthracen-9-yl)-5-(4-nitrophenyl)-4,5-dihydro-1...)
Affinity DataKi:  20.1nMAssay Description:Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425409(CHEMBL2312575)
Affinity DataKi:  21nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425412(CHEMBL2312285)
Affinity DataKi:  24nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425408(CHEMBL2312576)
Affinity DataKi:  25nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425413(CHEMBL2312284)
Affinity DataKi:  30nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425417(CHEMBL2312282)
Affinity DataKi:  30nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341160(3-(anthracen-9-yl)-5-(3-nitrophenyl)-4,5-dihydro-1...)
Affinity DataKi:  32.2nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425410(CHEMBL2312574)
Affinity DataKi:  41nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341160(3-(anthracen-9-yl)-5-(3-nitrophenyl)-4,5-dihydro-1...)
Affinity DataKi:  43.9nMAssay Description:Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341157(2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  69.9nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341157(2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  77.6nMAssay Description:Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341158(4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  81.5nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBromodomain-containing protein 4(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50443232(CHEMBL3086883)
Affinity DataKi: <85nMAssay Description:Inhibition of human 6x-His-tagged BRD4 bromodomain 1 expressed in Escherichia coliMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341158(4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  95.7nMAssay Description:Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425415(CHEMBL2312577)
Affinity DataKi: >100nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425416(CHEMBL2312578)
Affinity DataKi: >100nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBromodomain-containing protein 3(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50443232(CHEMBL3086883)
Affinity DataKi:  100nMAssay Description:Inhibition of human 6x-His-tagged BRD3 bromodomain 1 expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50425414(CHEMBL2312283)
Affinity DataKi: >100nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBromodomain-containing protein 3(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50443232(CHEMBL3086883)
Affinity DataKi:  140nMAssay Description:Inhibition of human 6x-His-tagged BRD3 bromodomain 2 expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341159(2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  205nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341153(4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  225nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341161(3-(anthracen-9-yl)-5-(4-methoxyphenyl)-4,5-dihydro...)
Affinity DataKi:  230nMAssay Description:Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341159(2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...)
Affinity DataKi:  242nMAssay Description:Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341155(3-(anthracen-9-yl)-5-p-tolyl-4,5-dihydro-1H-pyrazo...)
Affinity DataKi:  250nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341154(3-(anthracen-9-yl)-5-(4-chlorophenyl)-4,5-dihydro-...)
Affinity DataKi:  281nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341161(3-(anthracen-9-yl)-5-(4-methoxyphenyl)-4,5-dihydro...)
Affinity DataKi:  301nMAssay Description:Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Birla Institute Of Technology

Curated by ChEMBL
LigandPNGBDBM50341154(3-(anthracen-9-yl)-5-(4-chlorophenyl)-4,5-dihydro-...)
Affinity DataKi:  320nMAssay Description:Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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