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Found 11 Enz. Inhib. hit(s) with Target = 'Leucine-rich repeat serine/threonine-protein kinase 2' and Ligand = 'BDBM257207'
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataIC50:  0.400nMAssay Description:Inhibition of full length LRRK2 G2019S mutant (unknown origin) by LRRKtide Adapta assayMore data for this Ligand-Target Pair
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataIC50:  0.400nMAssay Description:Inhibition of full-length LRRK2 G2019S mutant (unknown origin) using LRRKtide as substrate incubated for 1 hr in presence of ATP by TR-FRET based ADA...More data for this Ligand-Target Pair
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataIC50:  0.5nMAssay Description:Inhibition of LRRK2 (unknown origin)More data for this Ligand-Target Pair
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataIC50:  0.5nMMore data for this Ligand-Target Pair
In DepthDetails PDB3D3D Structure (crystal)
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataIC50:  0.800nMAssay Description:Inhibition of recombinant human GST-tagged LRRK2 G2019S mutant catalytic domain (970 to 2527 residues) expressed in baculovirus expression system usi...More data for this Ligand-Target Pair
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataIC50:  1nMAssay Description:Inhibition of full-length wild type LRRK2 (unknown origin) using LRRKtide as substrate incubated for 1 hr in presence of ATP by TR-FRET based ADAPTA ...More data for this Ligand-Target Pair
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataIC50:  1nMAssay Description:Inhibition of full length wild type LRRK2 (unknown origin) by LRRKtide Adapta assayMore data for this Ligand-Target Pair
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataIC50:  1.20nMMore data for this Ligand-Target Pair
In DepthDetails PDB3D3D Structure (crystal)
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataEC50:  23nMAssay Description:Inhibition of wild type pcDNA5FRT-TO-GFP fused - LRRK2 (unknown origin) transfected in HEK293 cells incubated for 24 hrs by ELISAMore data for this Ligand-Target Pair
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Homo sapiens (Human))
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataEC50:  30nMAssay Description:Inhibition of pcDNA5FRT-TO-GFP fused - LRRK2 G2019S mutant (unknown origin) transfected in HEK293 cells incubated for 24 hrs by ELISAMore data for this Ligand-Target Pair
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Mus musculus)
Stanford University

Curated by ChEMBL
LigandPNGBDBM257207(US9493440, 51)
Affinity DataEC50:  30nMAssay Description:Inhibition of mouse full-length LRRK2 G2019S mutant transfected in HEK293 cells using LRRKtide as substrate in presence of ATP by incubated for 1 hr ...More data for this Ligand-Target Pair