BDBM50211441 4-(4-(1H-indol-3-yl)pyrimidin-2-ylamino)-N-ethylpiperidine-1-carboxamide::CHEMBL245725

SMILES CCNC(=O)N1CCC(CC1)Nc1nccc(n1)-c1c[nH]c2ccccc12

InChI Key InChIKey=KAEBPVNZHCYYSN-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50211441   

TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50211441(4-(4-(1H-indol-3-yl)pyrimidin-2-ylamino)-N-ethylpi...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of CDK2 by IMAP technologyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50211441(4-(4-(1H-indol-3-yl)pyrimidin-2-ylamino)-N-ethylpi...)
Affinity DataIC50:  245nMAssay Description:Inhibition of JNK2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTranscription factor Jun(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50211441(4-(4-(1H-indol-3-yl)pyrimidin-2-ylamino)-N-ethylpi...)
Affinity DataIC50:  8.09E+3nMAssay Description:Inhibition of cJun translocation in IL1beta-stimulated A549 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Ucb Pharma

Curated by ChEMBL
LigandPNGBDBM50211441(4-(4-(1H-indol-3-yl)pyrimidin-2-ylamino)-N-ethylpi...)
Affinity DataIC50:  74nMAssay Description:Inhibition of JNK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed