BDBM50335237 3-(1H-indol-3-yl)-4-[2-(4-oxo-piperidin-1-yl)-5-trifluoromethyl-ylpyrimidin-4-yl]-pyrrole-2,5-dione::3-(1H-indol-3-yl)-4-[2-(4-oxopiperidin-1-yl)-5-(trifluoromethyl)pyrimidin-4-yl]-1H-pyrrole-2,5-dione::CHEMBL1235315

SMILES c1ccc2c(c1)c(c[nH]2)C3=C(C(=O)NC3=O)c4c(cnc(n4)N5CCC(=O)CC5)C(F)(F)F

InChI Key InChIKey=MYIILBMNTUDZDH-UHFFFAOYSA-N

Data  7 IC50

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50335237   

TargetTyrosine-protein kinase JAK3(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50335237BDBM50335237(3-(1H-indol-3-yl)-4-[2-(4-oxo-piperidin-1-yl)-5-tr...)
Affinity DataIC50: 27nMAssay Description:Inhibition of GST-tagged Jak3 expressed in insect cells using 18 uM ATPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/4/2013
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein kinase JAK3(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50335237BDBM50335237(3-(1H-indol-3-yl)-4-[2-(4-oxo-piperidin-1-yl)-5-tr...)
Affinity DataIC50: 27nMAssay Description:Inhibition of N-terminal GST-tagged human recombinant JAK3 (811 to 1103 residues) extracted from Sf9 cells incubated for 60 mins by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMedPDB3D3D Structure (crystal)
TargetTyrosine-protein kinase JAK1(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50335237BDBM50335237(3-(1H-indol-3-yl)-4-[2-(4-oxo-piperidin-1-yl)-5-tr...)
Affinity DataIC50: 253nMAssay Description:Inhibition of GST-tagged Jak1 expressed in insect cells using 70 uM ATPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/4/2013
Entry Details Article
PubMed
TargetTyrosine-protein kinase JAK1(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50335237BDBM50335237(3-(1H-indol-3-yl)-4-[2-(4-oxo-piperidin-1-yl)-5-tr...)
Affinity DataIC50: 253nMAssay Description:Inhibition of recombinant N-terminal GST-tagged JAK1 (unknown origin) extracted from Sf9 cells by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50335237BDBM50335237(3-(1H-indol-3-yl)-4-[2-(4-oxo-piperidin-1-yl)-5-tr...)
Affinity DataIC50: 330nMAssay Description:Inhibition of recombinant N-terminal GST-tagged JAK2 (unknown origin) extracted from Sf9 cells using FITC-KGGEEEEYFE as substrate measured for 1 hr b...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
China Pharmaceutical University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50335237BDBM50335237(3-(1H-indol-3-yl)-4-[2-(4-oxo-piperidin-1-yl)-5-tr...)
Affinity DataIC50: 330nMAssay Description:Inhibition of GST-tagged Jak2 expressed in insect cells using 20 uM ATPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/4/2013
Entry Details Article
PubMed
TargetNon-receptor tyrosine-protein kinase TYK2(Human)
Novartis Institutes For Biomedical Research

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50335237BDBM50335237(3-(1H-indol-3-yl)-4-[2-(4-oxo-piperidin-1-yl)-5-tr...)
Affinity DataIC50: 4.33E+3nMAssay Description:Inhibition of GST-tagged Tyk2 expressed in insect cells using 35 uM ATPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/4/2013
Entry Details Article
PubMed