BDBM515659 BDBM515661::US11053219, Example 28::US11053219, Example 50::US11731956, Example 50
SMILES CNC(=O)c1nnc(NC(=O)N2CCC2)cc1Nc1cccc(-c2ncn(C)n2)c1OC
InChI Key InChIKey=SBJKITGOXSWAGF-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 15 hits for monomerid = 515659
Affinity DataKd: <1nMAssay Description:DiscoverX's KINOMEscan is a popular platform for kinase profiling, frequently used in academic and industry witnessed by publications, ther...More data for this Ligand-Target Pair
Affinity DataKd: <1nMAssay Description:DiscoverX's KINOMEscan is a popular platform for kinase profiling, frequently used in academic and industry witnessed by publications, ther...More data for this Ligand-Target Pair
Affinity DataKd: <1nMAssay Description:DiscoverX's KINOMEscan is a popular platform for kinase profiling, frequently used in academic and industry witnessed by publications, ther...More data for this Ligand-Target Pair
Affinity DataKd: <1nMAssay Description:Developed by DiscoverX, KINOMEscan employs proprietary active-site dependent competition binding assays to determine how compounds bind to kinases. K...More data for this Ligand-Target Pair
Affinity DataKd: <1nMAssay Description:Developed by DiscoverX, KINOMEscan employs proprietary active-site dependent competition binding assays to determine how compounds bind to kinases. K...More data for this Ligand-Target Pair
Affinity DataKd: <1nMAssay Description:Developed by DiscoverX, KINOMEscan employs proprietary active-site dependent competition binding assays to determine how compounds bind to kinases. K...More data for this Ligand-Target Pair
Affinity DataKd: 0.0280nMAssay Description:Binding affinity to human wild-type partial length TYK2 JH2 (G556 to D888 residues) expressed in mammalian expression system by KINOMEscan assayMore data for this Ligand-Target Pair
Affinity DataKd: 3.70nMAssay Description:Binding affinity to JAK1 JH2 (unknown origin)More data for this Ligand-Target Pair
TargetSignal transducer and activator of transcription 3(Human)
China Pharmaceutical University
Curated by ChEMBL
China Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 28nMAssay Description:Inhibition of IL-23 induced STAT3 phosphorylation in human KIT225 cells by AlphaLISA assayMore data for this Ligand-Target Pair
Affinity DataKd: 290nMAssay Description:Binding affinity to wild-type partial length human recombinant JAK2 JH2 (unknown origin) (A829 to G1132 residues) expressed in mammalian expression s...More data for this Ligand-Target Pair
Affinity DataKd: >2.00E+4nMAssay Description:Binding affinity to wild-type partial length human recombinant JAK1 JH1 (unknown origin) (V856 to K1154 residues) expressed in bacterial expression s...More data for this Ligand-Target Pair
Affinity DataKd: 6.50E+3nMAssay Description:Binding affinity to wild-type partial length human recombinant JAK2 JH1 (unknown origin) (A829 to G1132 residues) expressed in mammalian expression s...More data for this Ligand-Target Pair
Affinity DataKd: 3.70E+3nMAssay Description:Binding affinity to wild-type partial length human recombinant JAK3 JH1 (unknown origin) (I781 to S1124 residues) expressed in mammalian expression s...More data for this Ligand-Target Pair
Affinity DataIC50: 54nMAssay Description:Inhibition of TYK2 JH2 in human KIT225 cells assessed as reduction of IFNalpha induced STAT1 phosphorylation by AlphaLISA assayMore data for this Ligand-Target Pair
TargetSignal transducer and activator of transcription 3(Human)
China Pharmaceutical University
Curated by ChEMBL
China Pharmaceutical University
Curated by ChEMBL
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibition of IL-6 induced STAT3 phosphorylation in human TF-1 cells by AlphaLISA assayMore data for this Ligand-Target Pair