BDBM50612230 CHEMBL5270706

SMILES CN1c2nnnn2C(C)(C)C(C(=O)Nc2ccc3[nH]nc(-c4ccnc(c4)N4CCOCC4)c3c2)=C1C

InChI Key InChIKey=VTISWVCQZDZSAV-UHFFFAOYSA-N

Data  10 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 10 hits for monomerid = 50612230   

LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  0.300nMAssay Description:Inhibition of N-terminal GST-fused human wild type LRRK2 using fluorescein-labeled LRRKtide as substrate preincubated for 15 mins followed by substra...More data for this Ligand-Target Pair
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LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50: <0.200nMAssay Description:Inhibition of N-terminal GST-fused human LRRK2 G2019S mutant using fluorescein-labeled LRRKtide as substrate preincubated for 15 mins followed by sub...More data for this Ligand-Target Pair
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LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  145nMAssay Description:Inhibition of human wild type LRRK2 expressed in HEK293 cells assessed as reduction in pSer935 phosphorylation incubated for 2 hrs by HTRF analysisMore data for this Ligand-Target Pair
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LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human LRRK2 G2019S mutant expressed in HEK293 cells assessed as reduction in pSer935 phosphorylation incubated for 2 hrs by HTRF analys...More data for this Ligand-Target Pair
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LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  4.70nMAssay Description:Inhibition human LRRK2 G2019S mutant expressed in human HEK293 assessed as Rab10 substrate phosphorylation at Threonine 73 residue incubated for 2 hr...More data for this Ligand-Target Pair
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LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  1.5nMAssay Description:Inhibition of human LRRK2 G2019S mutant expressed in HEK293 cells assessed as reduction in pSer935 phosphorylation incubated for 2 hrs by immunoblott...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  34nMAssay Description:Inhibition of human wild type LRRK2 expressed in HEK293 cells assessed as reduction in pS1292 phosphorylation incubated for 2 hrs by MSD analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  1nMAssay Description:Inhibition of human LRRK2 G2019S mutant expressed in HEK293 cells assessed as reduction in pS1292 phosphorylation incubated for 2 hrs by MSD analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  473nMAssay Description:Inhibition human wild type LRRK2 expressed in human HEK293 assessed as Rab10 substrate phosphorylation at Threonine 73 residue incubated for 2 hrs by...More data for this Ligand-Target Pair
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LigandPNGBDBM50612230(CHEMBL5270706)
Affinity DataIC50:  259nMAssay Description:Inhibition of human wild type LRRK2 expressed in HEK293 cells assessed as reduction in pSer935 phosphorylation incubated for 2 hrs by immunoblotting ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed