Compound Info
NAs Base Info
ID Cluster Name Target MolWt
Compound Structure
NAs.003147 7
Target name Tax id
MAP kinase p38 delta 9606.0
Serine/threonine-protein kinase Aurora-B 9606.0
Tyrosine-protein kinase JAK2 9606.0
Fibroblast growth factor receptor 1 9606.0
Ribosomal protein S6 kinase 1 9606.0
Mitogen-activated protein kinase kinase kinase 9 9606.0
Maternal embryonic leucine zipper kinase 9606.0
MAP kinase ERK2 9606.0
Serine/threonine-protein kinase Sgk1 9606.0
Ribosomal protein S6 kinase alpha 5 9606.0
Inhibitor of nuclear factor kappa B kinase beta subunit 9606.0
Serine/threonine-protein kinase PAK 2 9606.0
Mitogen-activated protein kinase kinase kinase kinase 2 9606.0
CaM-kinase kinase beta 9606.0
MAP kinase-activated protein kinase 3 9606.0
Tyrosine-protein kinase LCK 9606.0
Death-associated protein kinase 1 9606.0
Serine/threonine-protein kinase PIM1 9606.0
Insulin receptor-related protein 9606.0
MAP kinase-activated protein kinase 5 9606.0
Cyclin-dependent kinase 2/cyclin E1 9606.0
Rho-associated protein kinase 2 9606.0
Serine/threonine-protein kinase c-TAK1 9606.0
Aurora kinase A/B 9606.0
Protein kinase C mu 9606.0
MAP kinase ERK1 9606.0
Serine/threonine-protein kinase PIM2 9606.0
Ephrin type-A receptor 2 9606.0
Protein kinase C gamma 9606.0
Inhibitor of nuclear factor kappa B kinase epsilon subunit 9606.0
Ephrin type-A receptor 4 9606.0
Cyclin-dependent kinase 2/cyclin A 9606.0
MAP kinase signal-integrating kinase 2 9606.0
MAP kinase p38 alpha 9606.0
Ribosomal protein S6 kinase alpha 1 9606.0
Dual specificity mitogen-activated protein kinase kinase 1 9606.0
Serine/threonine-protein kinase AKT 9606.0
Serine/threonine-protein kinase PIM3 9606.0
Serine/threonine-protein kinase PLK1 9606.0
BR serine/threonine-protein kinase 1 9606.0
Mitogen-activated protein kinase kinase kinase 5 9606.0
Serine/threonine-protein kinase Aurora-A 9606.0
MAP kinase-activated protein kinase 2 9606.0
Myosin light chain kinase 9606.0
smooth muscle 9606.0
Dual specificity mitogen-activated protein kinase kinase 2 9606.0
AMP-activated protein kinase 9606.0
alpha-2 subunit 9606.0
Homeodomain-interacting protein kinase 3 9606.0
Casein kinase II 9606.0
Receptor protein-tyrosine kinase erbB-4 9606.0
MAP/microtubule affinity-regulating kinase 4 9606.0
Serine/threonine-protein kinase RIPK2 9606.0
Tyrosine-protein kinase CSK 9606.0
Phosphorylase kinase 9606.0
Serine/threonine-protein kinase tousled-like 1 9606.0
Serine/threonine-protein kinase AKT2 9606.0
Tyrosine-protein kinase ZAP-70 9606.0
Insulin-like growth factor I receptor 9606.0
Serine/threonine-protein kinase TAO1 9606.0
MAP/microtubule affinity-regulating kinase 2 9606.0
Serine/threonine-protein kinase PAK6 9606.0
Serine/threonine-protein kinase NEK2 9606.0
Ephrin type-B receptor 1 9606.0
Serine/threonine-protein kinase MST2 9606.0
Serine/threonine-protein kinase NEK6 9606.0
Ribosomal protein S6 kinase alpha 3 9606.0
Dual-specificity tyrosine-phosphorylation regulated kinase 3 9606.0
Mitogen-activated protein kinase kinase kinase 1 9606.0
Dual specificity protein kinase TTK 9606.0
Serine/threonine-protein kinase MARK1 9606.0
Tyrosine-protein kinase SYK 9606.0
Tyrosine-protein kinase ABL 9606.0
Protein kinase C zeta 9606.0
Cyclin-dependent kinase 1/cyclin B1 9606.0
Mitogen-activated protein kinase kinase kinase 11 9606.0
CaM kinase I alpha 9606.0
MAP kinase-interacting serine/threonine-protein kinase MNK1 9606.0
Glycogen synthase kinase-3 beta 9606.0
Serine/threonine-protein kinase PAK 4 9606.0
Dual specificity mitogen-activated protein kinase kinase 6 9606.0
Tyrosine-protein kinase BTK 9606.0
Serine/threonine-protein kinase OSR1 9606.0
Dual-specificity tyrosine-phosphorylation regulated kinase 1A 9606.0
MAP kinase p38 beta 9606.0
BR serine/threonine-protein kinase 2 9606.0
Tyrosine-protein kinase BRK 9606.0
c-Jun N-terminal kinase 1 9606.0
Mitogen-activated protein kinase kinase kinase 7 9606.0
Homeodomain-interacting protein kinase 2 9606.0
Serine/threonine-protein kinase 33 9606.0
Mitogen-activated protein kinase 15 9606.0
Protein kinase C alpha 9606.0
Serine/threonine-protein kinase 16 9606.0
Ephrin type-B receptor 4 9606.0
Protein kinase N2 9606.0
Interleukin-1 receptor-associated kinase 4 9606.0
MAP kinase p38 gamma 9606.0
Ephrin type-B receptor 2 9606.0
Eukaryotic translation initiation factor 2-alpha kinase 3 9606.0
c-Jun N-terminal kinase 2 9606.0
Insulin receptor 9606.0
Dual-specificity tyrosine-phosphorylation regulated kinase 2 9606.0
Interleukin-1 receptor-associated kinase 1 9606.0
Dual specificity protein kinase CLK2 9606.0
Serine/threonine-protein kinase EEF2K 9606.0
Homeodomain-interacting protein kinase 1 9606.0
Misshapen-like kinase 1 9606.0
Serine/threonine-protein kinase MST4 9606.0
Serine/threonine-protein kinase SRPK1 9606.0
Serine/threonine-protein kinase TBK1 9606.0
Tyrosine-protein kinase TIE-2 9606.0
Tyrosine-protein kinase SRC 9606.0
Serine/threonine-protein kinase 11 9606.0
Nerve growth factor receptor Trk-A 9606.0
c-Jun N-terminal kinase 3 9606.0
NUAK family SNF1-like kinase 1 9606.0
Serine/threonine-protein kinase Chk2 9606.0
Tyrosine-protein kinase YES 9606.0
Pyruvate dehydrogenase kinase isoform 1 9606.0
Serine/threonine-protein kinase Chk1 9606.0
306.374
Chemical Representations
InChI InChI=1S/C13H22N8O/c1-4-8(5-22)17-13-19-10(18-12(14)15)9-11(20-13)21(6-16-9)7(2)3/h6-8,22H,4-5H2,1-3H3,(H5,14,15,17,18,19,20)/t8-/m1/s1
InChI Key LSLSNRQKKSMLCT-MRVPVSSYSA-N
SMILES CC[C@H](CO)Nc1nc(NC(=N)N)c2ncn(C(C)C)c2n1
Molecular Formula C13H22N8O
Functional Fragments
Base Ribose Phosphate
Base Structure
Match
No Image Available
Match
Calculated Properties
logP 0.895 Computed by RDKit
Heavy Atom Count 22 Computed by RDKit
Ring Count 2 Computed by RDKit
Hydrogen Bond Acceptor Count 7 Computed by RDKit
Hydrogen Bond Donor Count 5 Computed by RDKit
Rotatable Bond Count 6 Computed by RDKit
Topological Polar Surface Area 137.760 Computed by RDKit
Activity Data
Target Activity type Relation Value Unit Assay Source
Misshapen-like kinase 1 Activity = 64.0 % Inhibition of recombinant MINK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Aurora kinase A/B Ratio = 0.08 Activity at Aurora kinase A/B in human MCF7 cells assessed as histone H3 phosphorylation at Ser10 at 100 uM after 24 hrs by flow cytometry relative to untreated control CHEMBL2331324
Tyrosine-protein kinase ZAP-70 Activity = 86.0 % Inhibition of recombinant ZAP70 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase YES Activity = 13.0 % Inhibition of recombinant YES1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Unchecked Activity = 6.0 % Inhibition of recombinant VEGFR (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Dual specificity protein kinase TTK Activity = 40.0 % Inhibition of recombinant TTK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Nerve growth factor receptor Trk-A Activity = 24.0 % Inhibition of recombinant TRKA (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase tousled-like 1 Activity = 9.0 % Inhibition of recombinant TLK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase TIE-2 Activity = 39.0 % Inhibition of recombinant TIE2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase TBK1 Activity = 92.0 % Inhibition of recombinant TBK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase TAO1 Activity = 9.0 % Inhibition of recombinant TAO1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Mitogen-activated protein kinase kinase kinase 7 Activity = 7.0 % Inhibition of recombinant TAK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase SYK Activity = 58.0 % Inhibition of recombinant SYK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase 33 Activity = 11.0 % Inhibition of recombinant STK33 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase SRPK1 Activity = 22.0 % Inhibition of recombinant SRPK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase SRC Activity = 22.0 % Inhibition of recombinant SRC (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Myosin light chain kinase, smooth muscle Activity = 49.0 % Inhibition of recombinant SMMLCK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase Sgk1 Activity = 60.0 % Inhibition of recombinant SGK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ribosomal protein S6 kinase 1 Activity = 49.0 % Inhibition of recombinant S6K1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ribosomal protein S6 kinase alpha 3 Activity = 35.0 % Inhibition of recombinant RSK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ribosomal protein S6 kinase alpha 1 Activity = 18.0 % Inhibition of recombinant RSK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Rho-associated protein kinase 2 Activity = 61.0 % Inhibition of recombinant ROCK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase RIPK2 Activity = 72.0 % Inhibition of recombinant RIPK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Protein kinase N2 Activity = 85.0 % Inhibition of recombinant PRK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase-activated protein kinase 5 Activity = 76.0 % Inhibition of recombinant PRAK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase PLK1 Activity = 108.0 % Inhibition of recombinant PLK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Protein kinase C mu Activity = 17.0 % Inhibition of recombinant PKD1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Protein kinase C gamma Activity = 73.0 % Inhibition of recombinant PKCgamma (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Protein kinase C zeta Activity = 68.0 % Inhibition of recombinant PKCzeta (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Protein kinase C alpha Activity = 71.0 % Inhibition of recombinant PKCalpha (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase AKT2 Activity = 111.0 % Inhibition of recombinant PKB beta (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase AKT Activity = 99.0 % Inhibition of recombinant PKB alpha (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Unchecked Activity = 90.0 % Inhibition of recombinant PKA (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase PIM3 Activity = 64.0 % Inhibition of recombinant PIM3 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase PIM2 Activity = 88.0 % Inhibition of recombinant PIM2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase PIM1 Activity = 85.0 % Inhibition of recombinant PIM1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Phosphorylase kinase Activity = 14.0 % Inhibition of recombinant PHK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Pyruvate dehydrogenase kinase isoform 1 Activity = 68.0 % Inhibition of recombinant PDK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase PAK6 Activity = 26.0 % Inhibition of recombinant PAK6 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase PAK6 Activity = 18.0 % Inhibition of recombinant PAK5 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase PAK 4 Activity = 15.0 % Inhibition of recombinant PAK4 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase PAK 2 Activity = 45.0 % Inhibition of recombinant PAK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase p38 gamma Activity = 77.0 % Inhibition of recombinant p38 MAPKgamma (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase p38 delta Activity = 37.0 % Inhibition of recombinant p38 MAPKdelta (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase p38 beta Activity = 64.0 % Inhibition of recombinant p38 MAPKbeta (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase p38 alpha Activity = 87.0 % Inhibition of recombinant p38 MAPKalpha (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase OSR1 Activity = 16.0 % Inhibition of recombinant OSR1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
NUAK family SNF1-like kinase 1 Activity = 8.0 % Inhibition of recombinant NUAK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase NEK6 Activity = 95.0 % Inhibition of recombinant NEK6 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase NEK2 Activity = 73.0 % Inhibition of recombinant NEK2a (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase MST4 Activity = 42.0 % Inhibition of recombinant MST4 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase MST2 Activity = 35.0 % Inhibition of recombinant MST2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ribosomal protein S6 kinase alpha 5 Activity = 46.0 % Inhibition of recombinant MSK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase 16 Activity = 36.0 % Inhibition of recombinant MPSK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase signal-integrating kinase 2 Activity = 119.0 % Inhibition of recombinant MNK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase-interacting serine/threonine-protein kinase MNK1 Activity = 173.0 % Inhibition of recombinant MNK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Mitogen-activated protein kinase kinase kinase 11 Activity = 37.0 % Inhibition of recombinant MLK3 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Mitogen-activated protein kinase kinase kinase 9 Activity = 25.0 % Inhibition of recombinant MLK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Dual specificity mitogen-activated protein kinase kinase 6 Activity = 72.0 % Inhibition of recombinant MKK6 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Dual specificity mitogen-activated protein kinase kinase 2 Activity = 53.0 % Inhibition of recombinant MKK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Dual specificity mitogen-activated protein kinase kinase 1 Activity = 41.0 % Inhibition of recombinant MKK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Maternal embryonic leucine zipper kinase Activity = 27.0 % Inhibition of recombinant MELK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Mitogen-activated protein kinase kinase kinase 1 Activity = 91.0 % Inhibition of recombinant MEKK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP/microtubule affinity-regulating kinase 4 Activity = 38.0 % Inhibition of recombinant MARK4 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase c-TAK1 Activity = 24.0 % Inhibition of recombinant MARK3 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP/microtubule affinity-regulating kinase 2 Activity = 45.0 % Inhibition of recombinant MARK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase MARK1 Activity = 31.0 % Inhibition of recombinant MARK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase-activated protein kinase 3 Activity = 80.0 % Inhibition of recombinant MAPKAPK3 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase-activated protein kinase 2 Activity = 41.0 % Inhibition of recombinant MAPKAPK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase 11 Activity = 13.0 % Inhibition of recombinant LKB1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase LCK Activity = 13.0 % Inhibition of recombinant LCK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
c-Jun N-terminal kinase 3 Activity = 96.0 % Inhibition of recombinant JNK3 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
c-Jun N-terminal kinase 2 Activity = 85.0 % Inhibition of recombinant JNK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
c-Jun N-terminal kinase 1 Activity = 88.0 % Inhibition of recombinant JNK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase JAK2 Activity = 16.0 % Inhibition of recombinant JAK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Insulin receptor-related protein Activity = 19.0 % Inhibition of recombinant IRR (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Interleukin-1 receptor-associated kinase 4 Activity = 21.0 % Inhibition of recombinant IRAK4 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Interleukin-1 receptor-associated kinase 1 Activity = 26.0 % Inhibition of recombinant IRAK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Insulin receptor Activity = 5.0 % Inhibition of recombinant IR (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Inhibitor of nuclear factor kappa B kinase epsilon subunit Activity = 66.0 % Inhibition of recombinant IKKepsilon (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Inhibitor of nuclear factor kappa B kinase beta subunit Activity = 74.0 % Inhibition of recombinant IKKbeta (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Insulin-like growth factor I receptor Activity = 10.0 % Inhibition of recombinant IGF-1R (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase Chk2 Activity = 59.0 % Inhibition of recombinant CHK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase Chk1 Activity = 58.0 % Inhibition of recombinant CHK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Homeodomain-interacting protein kinase 3 Activity = 38.0 % Inhibition of recombinant HIPK3 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Homeodomain-interacting protein kinase 2 Activity = 8.0 % Inhibition of recombinant HIPK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Homeodomain-interacting protein kinase 1 Activity = 15.0 % Inhibition of recombinant HIPK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Receptor protein-tyrosine kinase erbB-4 Activity = 27.0 % Inhibition of recombinant HER4 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Glycogen synthase kinase-3 beta Activity = 37.0 % Inhibition of recombinant GSK3b (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Mitogen-activated protein kinase kinase kinase kinase 2 Activity = 15.0 % Inhibition of recombinant GCK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Fibroblast growth factor receptor 1 Activity = 4.0 % Inhibition of recombinant FGF-R1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Mitogen-activated protein kinase 15 Activity = 16.0 % Inhibition of recombinant ERK8 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase ERK2 Activity = 32.0 % Inhibition of recombinant ERK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MAP kinase ERK1 Activity = 50.0 % Inhibition of recombinant ERK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ephrin type-B receptor 4 Activity = 6.0 % Inhibition of recombinant EPH-B4 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ephrin type-B receptor 2 Activity = 2.0 % Inhibition of recombinant EPH-B2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ephrin type-B receptor 1 Activity = 8.0 % Inhibition of recombinant EPH-B1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ephrin type-A receptor 4 Activity = 22.0 % Inhibition of recombinant EPH-A4 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Ephrin type-A receptor 2 Activity = 22.0 % Inhibition of recombinant EPH-A2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Eukaryotic translation initiation factor 2-alpha kinase 3 Activity = 17.0 % Inhibition of recombinant EIF2AK3 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase EEF2K Activity = 94.0 % Inhibition of recombinant EF2K (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Dual-specificity tyrosine-phosphorylation regulated kinase 3 Activity = 18.0 % Inhibition of recombinant DYRK3 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Dual-specificity tyrosine-phosphorylation regulated kinase 2 Activity = 27.0 % Inhibition of recombinant DYRK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Dual-specificity tyrosine-phosphorylation regulated kinase 1A Activity = 1.0 % Inhibition of recombinant DYRK1A (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Death-associated protein kinase 1 Activity = 54.0 % Inhibition of recombinant DAPK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase CSK Activity = 58.0 % Inhibition of recombinant CSK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Dual specificity protein kinase CLK2 Activity = 4.0 % Inhibition of recombinant CLK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Casein kinase II Activity = 43.0 % Inhibition of recombinant CK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Unchecked Activity = 15.0 % Inhibition of recombinant CK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Cyclin-dependent kinase 2/cyclin A Activity = 5.0 % Inhibition of recombinant CDK2/cyclin A (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
CaM-kinase kinase beta Activity = 17.0 % Inhibition of recombinant CAMKKbeta (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
CaM kinase I alpha Activity = 35.0 % Inhibition of recombinant CAMK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase BTK Activity = 53.0 % Inhibition of recombinant BTK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
BR serine/threonine-protein kinase 2 Activity = 77.0 % Inhibition of recombinant BRSK2 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
BR serine/threonine-protein kinase 1 Activity = 44.0 % Inhibition of recombinant BRSK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase BRK Activity = 50.0 % Inhibition of recombinant BRK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase Aurora-B Activity = 47.0 % Inhibition of recombinant AURB (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Serine/threonine-protein kinase Aurora-A Activity = 39.0 % Inhibition of recombinant AURA (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Mitogen-activated protein kinase kinase kinase 5 Activity = 100.0 % Inhibition of recombinant ASK1 (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
AMP-activated protein kinase, alpha-2 subunit Activity = 29.0 % Inhibition of recombinant AMPK (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
Tyrosine-protein kinase ABL Activity = 5.0 % Inhibition of recombinant ABL (unknown origin) assessed as residual activity using [gamma-33P]ATP as substrate at 1 uM CHEMBL2331324
MCF7 Ratio = 1.8 Cell cycle arrest in human MCF7 cells assessed as accumulation of cells in G2+M phase at 100 uM after 24 hrs by propidium iodide staining based flow cytometry relative to untreated control CHEMBL2331324
MCF7 IC50 = 4500.0 nM Cytotoxicity against human MCF7 cells assessed as inhibition of cell viability after 72 hrs by calcien AM dye based fluorescence analysis CHEMBL2331324
Cyclin-dependent kinase 2/cyclin E1 IC50 = 140.0 nM Inhibition of recombinant CDK2/cyclin E (unknown origin) using histone H1 as substrate in presence of [gamma-33P]ATP CHEMBL2331324
Cyclin-dependent kinase 1/cyclin B1 IC50 = 2100.0 nM Inhibition of recombinant CDK1/cyclin B (unknown origin) using histone H1 as substrate in presence of [gamma-33P]ATP CHEMBL2331324