BDBM50624647 CHEMBL5396660

SMILES Cc1[nH]nc(c1-c1cc(F)c(N2CCC3(C2)CCS(=O)(=O)CC3)c(F)c1)-c1ccncc1

InChI Key InChIKey=ZTQLTVVZCKVDKJ-UHFFFAOYSA-N

Data  2 IC50  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50624647   

TargetLeucine-rich repeat serine/threonine-protein kinase 2(Human)
Stanford University

Curated by ChEMBL
LigandPNGBDBM50624647(CHEMBL5396660)
Affinity DataIC50: 49nMAssay Description:Inhibition of wildtype full length LRRK2 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Human)
Stanford University

Curated by ChEMBL
LigandPNGBDBM50624647(CHEMBL5396660)
Affinity DataIC50: 4.60nMAssay Description:Inhibition of LRRK2 G2019S mutant (unknown origin)More data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Human)
Stanford University

Curated by ChEMBL
LigandPNGBDBM50624647(CHEMBL5396660)
Affinity DataEC50: >1.00E+5nMAssay Description:Inhibition of wildtype full length LRRK2 in HEK293 cellsMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetLeucine-rich repeat serine/threonine-protein kinase 2(Human)
Stanford University

Curated by ChEMBL
LigandPNGBDBM50624647(CHEMBL5396660)
Affinity DataEC50:  140nMAssay Description:Inhibition of LRRK2 G2019S mutant in HEK293 cellsMore data for this Ligand-Target Pair
Ligand InfoSimilars
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed