TargetPoly(ADP-ribose) glycohydrolase(Homo sapiens (Human))
Tokyo University Of Science
Curated by ChEMBL
Tokyo University Of Science
Curated by ChEMBL
Affinity DataIC50: 2.97E+4nMAssay Description:Inhibition of recombinant human PARG assessed as mono(ADP-R) release using PAR as substrate measured after 15 mins by HPLC analysisMore data for this Ligand-Target Pair
TargetPoly(ADP-ribose) glycohydrolase(Homo sapiens (Human))
Tokyo University Of Science
Curated by ChEMBL
Tokyo University Of Science
Curated by ChEMBL
Affinity DataIC50: 6.14E+4nMAssay Description:Inhibition of recombinant human PARG assessed as mono(ADP-R) release using PAR as substrate measured after 15 mins by HPLC analysisMore data for this Ligand-Target Pair
TargetPoly(ADP-ribose) glycohydrolase(Homo sapiens (Human))
Tokyo University Of Science
Curated by ChEMBL
Tokyo University Of Science
Curated by ChEMBL
Affinity DataIC50: 1.06E+5nMAssay Description:Inhibition of recombinant human PARG assessed as mono(ADP-R) release using PAR as substrate measured after 15 mins by HPLC analysisMore data for this Ligand-Target Pair
TargetPoly(ADP-ribose) glycohydrolase(Homo sapiens (Human))
Tokyo University Of Science
Curated by ChEMBL
Tokyo University Of Science
Curated by ChEMBL
Affinity DataIC50: 1.20E+5nMAssay Description:Inhibition of recombinant human PARG assessed as mono(ADP-R) release using PAR as substrate measured after 15 mins by HPLC analysisMore data for this Ligand-Target Pair
TargetPoly(ADP-ribose) glycohydrolase(Homo sapiens (Human))
Tokyo University Of Science
Curated by ChEMBL
Tokyo University Of Science
Curated by ChEMBL
Affinity DataIC50: >3.00E+5nMAssay Description:Inhibition of recombinant human PARG assessed as mono(ADP-R) release using PAR as substrate measured after 15 mins by HPLC analysisMore data for this Ligand-Target Pair