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Found 12 with Last Name = 'k?sa' and Initial = 'd'
TargetCholinesterase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM50600286(CHEMBL5174709)
Affinity DataIC50:  2.25E+3nMAssay Description:Inhibition of BChE (unknown origin) using acetylcholine iodide as substrate incubated for 10 mins by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetTyrosinase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM50600285(CHEMBL1831286)
Affinity DataIC50:  2.32E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate incubated for 10 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetCholinesterase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM50600285(CHEMBL1831286)
Affinity DataIC50:  2.82E+3nMAssay Description:Inhibition of BChE (unknown origin) using acetylcholine iodide as substrate incubated for 10 mins by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetTyrosinase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM50600286(CHEMBL5174709)
Affinity DataIC50:  2.83E+3nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate incubated for 10 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM50600286(CHEMBL5174709)
Affinity DataIC50:  4.76E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylcholine iodide as substrate incubated for 10 mins by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM50600285(CHEMBL1831286)
Affinity DataIC50:  5.66E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylcholine iodide as substrate incubated for 10 mins by Ellman's methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetTyrosinase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)
Affinity DataIC50:  2.45E+4nMAssay Description:Inhibition of tyrosinase (unknown origin) using L-DOPA as substrate incubated for 10 minsMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTyrosinase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM7460(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chrome...)
Affinity DataIC50:  4.44E+4nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTyrosinase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM7462(3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-...)
Affinity DataIC50:  6.51E+4nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTyrosinase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM50241244((E)-((2R,3S,4S,5R,6S)-6-(5,7-dihydroxy-2-(4-hydrox...)
Affinity DataIC50:  7.85E+4nMAssay Description:Inhibition of tyrosinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM8961(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)
Affinity DataIC50:  1.17E+5nMAssay Description:Inhibition of AChE (unknown origin) using acetylcholine iodide as substrate incubated for 10 mins by Ellman's methodMore data for this Ligand-Target Pair
TargetCholinesterase(Homo sapiens (Human))
Bartin University

Curated by ChEMBL
LigandPNGBDBM8961(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)
Affinity DataIC50:  1.25E+5nMAssay Description:Inhibition of BChE (unknown origin) using acetylcholine iodide as substrate incubated for 10 mins by Ellman's methodMore data for this Ligand-Target Pair