Reaction Details | |||
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Target | Serine/threonine-protein kinase pim-3 | ||
Ligand | BDBM377190 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Enzyme Assay | ||
IC50 | <100±n/a nM | ||
Citation | Xue, C; Li, Y; Feng, H; Zhang, K Thiazolecarboxamides and pyridinecarboxamide compounds useful as PIM kinase inhibitors US Patent US10517858 Publication Date 12/31/2019 | ||
More Info.: | Get all data from this article, Assay Method | ||
Serine/threonine-protein kinase pim-3 | |||
Name: | Serine/threonine-protein kinase pim-3 | ||
Synonyms: | PIM3 | PIM3_HUMAN | Serine/threonine-protein kinase pim-3 (PIM3) | ||
Type: | Protein | ||
Mol. Mass.: | 35888.19 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Q86V86 | ||
Residue: | 326 | ||
Sequence: |
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BDBM377190 | |||
n/a | |||
Name | BDBM377190 | ||
Synonyms: | N-{4-[(3S,5R)-3-Amino-5-methylpiperidin-1-yl]-2,3-dihydrofuro[2,3-b]pyridin-5-yl}-6-(2,6-difluorophenyl)-5-fluoropyridine-2-carboxamide | US10265307, Example 39 | US10517858, Example 39 | US10828290, Example 39 | US11229631, Example 39 | ||
Type | Small organic molecule | ||
Emp. Form. | C25H24F3N5O2 | ||
Mol. Mass. | 483.4856 | ||
SMILES | C[C@@H]1C[C@H](N)CN(C1)c1c2CCOc2ncc1NC(=O)c1ccc(F)c(n1)-c1c(F)cccc1F |r,wU:3.3,1.0,(-.15,2.69,;-1.48,1.93,;-2.82,2.69,;-4.15,1.93,;-5.48,2.69,;-4.15,.38,;-2.82,-.38,;-1.48,.38,;-2.82,-1.93,;-4.15,-2.69,;-5.61,-2.22,;-6.52,-3.47,;-5.61,-4.71,;-4.15,-4.23,;-2.82,-5,;-1.48,-4.23,;-1.48,-2.69,;-.15,-1.93,;1.18,-2.69,;1.18,-4.23,;2.52,-1.93,;3.85,-2.69,;5.19,-1.93,;5.19,-.38,;6.52,.38,;3.85,.38,;2.52,-.38,;3.85,1.93,;2.52,2.7,;1.18,1.93,;2.52,4.24,;3.85,5,;5.19,4.24,;5.19,2.7,;6.52,1.93,)| | ||
Structure |