BDBM30192 Pyrrolopyridine, 23

SMILES Fc1ccccc1-c1cc(ccn1)-c1cc2c(CCNC2=O)[nH]1

InChI Key InChIKey=XJJYJNMNYDNXNO-UHFFFAOYSA-N

Data  10 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 12 hits for monomerid = 30192   

LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 126nMpH: 7.5 T: 2°CAssay Description:The phosphorylation of HSP27 peptide by MAPKAPK2 was measured using an anion exchange resin capture assay method. The reaction was carried out in rea...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 1.10E+3nMpH: 7.5 T: 2°CAssay Description:Compounds were evaluated as inhibitors of kinase by measuring their effect on kinase induced phosphorylation of substrate. IC50 values were reported ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 210nMpH: 7.5 T: 2°CAssay Description:Compounds were evaluated as inhibitors of kinase by measuring their effect on kinase induced phosphorylation of substrate. IC50 values were reported ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 4.60E+3nMpH: 7.5 T: 2°CAssay Description:Compounds were evaluated as inhibitors of kinase by measuring their effect on kinase induced phosphorylation of substrate. IC50 values were reported ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 1.00E+4nMAssay Description:Compounds were evaluated as inhibitors of kinase by measuring their effect on kinase induced phosphorylation of substrate. IC50 values were reported ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 2.00E+5nMAssay Description:Compounds were evaluated as inhibitors of kinase by measuring their effect on kinase induced phosphorylation of substrate. IC50 values were reported ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 5.80E+4nMAssay Description:Compounds were evaluated as inhibitors of kinase by measuring their effect on kinase induced phosphorylation of substrate. IC50 values were reported ...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataEC50:  2.70E+3nMAssay Description:Inhibition of MK2 in LPS-stimulated human THP1 cells assessed as inhibition of Hsp27 phosphorylation pretreated 60 mins before LPS challenge measured...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataEC50:  372nMAssay Description:Inhibition of MK2 pretreated for 30 mins before fluorescein labeled substrate peptide addition measured after 2 hrs by IMAP assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 560nMAssay Description:Inhibition of human MK2 using biotinyl-AYSRALSRQLSSGVSEIRCOOH as substrate after 45 mins by FRET analysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 8.90E+3nMAssay Description:Inhibition of MK2 mediated anisomycin-stimulated hsp27 phosphorylation in human THP-1 cells by fluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTyrosine-protein kinase JAK3(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM30192(Pyrrolopyridine, 23)
Affinity DataIC50: 501nMAssay Description:Inhibition of JAK3 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed