Reaction Details | |||
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Target | Dual specificity protein kinase TTK | ||
Ligand | BDBM50569985 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_2110865 (CHEMBL4819715) | ||
Kd | 1.5±n/a nM | ||
Citation | Huang, M; Huang, Y; Guo, J; Yu, L; Chang, Y; Wang, X; Luo, J; Huang, Y; Tu, Z; Lu, X; Xu, Y; Zhang, Z; Zhang, Z; Ding, K Pyrido[2, 3-d]pyrimidin-7(8H)-ones as new selective orally bioavailable Threonine Tyrosine Kinase (TTK) inhibitors. Eur J Med Chem211:0 (2021) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Dual specificity protein kinase TTK | |||
Name: | Dual specificity protein kinase TTK | ||
Synonyms: | Dual specificity protein kinase (TTK) | Dual specificity protein kinase TTK (MPS1) | MPS1 | MPS1L1 | Monopolar Spindle 1 (MPS1) | Monopolar Spindle 1 (Mps-1) | Monopolar Spindle 1 Kinase (MPS1) | Phosphotyrosine picked threonine-protein kinase (MPS1) | TTK | TTK_HUMAN | ||
Type: | Protein | ||
Mol. Mass.: | 97086.79 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P33981 | ||
Residue: | 857 | ||
Sequence: |
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BDBM50569985 | |||
n/a | |||
Name | BDBM50569985 | ||
Synonyms: | CHEMBL4874692 | ||
Type | Small organic molecule | ||
Emp. Form. | C30H41N7O3 | ||
Mol. Mass. | 547.6916 | ||
SMILES | CCC(=O)N[C@H]1CC[C@H](CC1)n1c2nc(Nc3ccc(cc3OC)N3CCN(C)CC3)ncc2c(CC)cc1=O |r,wU:8.11,5.4,(26.59,-17.84,;26.61,-19.38,;25.28,-20.16,;25.3,-21.7,;23.94,-19.4,;23.93,-17.86,;22.59,-17.11,;22.57,-15.56,;23.9,-14.78,;25.24,-15.54,;25.25,-17.08,;23.88,-13.24,;22.54,-12.48,;21.22,-13.27,;19.87,-12.51,;18.54,-13.29,;17.2,-12.54,;17.19,-11,;15.85,-10.24,;14.52,-11.02,;14.54,-12.56,;15.88,-13.32,;15.89,-14.86,;14.57,-15.64,;13.17,-10.26,;11.85,-11.05,;10.51,-10.29,;10.49,-8.75,;9.15,-8,;11.82,-7.97,;13.16,-8.72,;19.85,-10.97,;21.18,-10.19,;22.53,-10.94,;23.85,-10.16,;23.84,-8.62,;25.16,-7.84,;25.19,-10.92,;25.21,-12.46,;26.55,-13.22,)| | ||
Structure |