BDBM50361289 CHEMBL1935608
SMILES [#6]-[#6](-[#6])-[#6]-[#6]\[#6]=[#6]\c1nc(-[#6]-[#6]-[#8]-c2ccc3-[#6]-[#6@H](-[#7](-[#6]-c3c2)-[#6](=O)\[#6]=[#6]\[#6]=[#6](\[#6])-[#6])-[#6](-[#8])=O)c(-[#6])o1
InChI Key InChIKey=SCOSJNWFMHSDBK-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50361289
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Kyoto Pharmaceutical Industries
Curated by ChEMBL
Kyoto Pharmaceutical Industries
Curated by ChEMBL
Affinity DataIC50: 950nMAssay Description:Inhibition of PTB1B using pNPP as substrate after 30 minsMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor alpha(Human)
Kyoto Pharmaceutical Industries
Curated by ChEMBL
Kyoto Pharmaceutical Industries
Curated by ChEMBL
Affinity DataEC50: 100nMAssay Description:Transactivation of human full length PPARalpha expressed in COS1 cells co-transfected with RXRalpha after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor gamma(Human)
Kyoto Pharmaceutical Industries
Curated by ChEMBL
Kyoto Pharmaceutical Industries
Curated by ChEMBL
Affinity DataEC50: 30nMAssay Description:Transactivation of human full length PPARgamma expressed in COS1 cells co-transfected with RXRalpha after 24 hrs by luciferase reporter gene assayMore data for this Ligand-Target Pair