Reaction Details |
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Target | Tyrosine-protein kinase JAK2 [828-1132] |
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Ligand | BDBM400285 |
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Substrate/Competitor | n/a |
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Meas. Tech. | In Vitro JAK Kinase Assay |
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IC50 | <5±n/a nM |
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Citation | Huang, T; Xue, C Piperidin-4-yl azetidine derivatives as JAK1 inhibitors US Patent US9999619 Publication Date 6/19/2018 |
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More Info.: | Get all data from this article, Assay Method |
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Tyrosine-protein kinase JAK2 [828-1132] |
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Name: | Tyrosine-protein kinase JAK2 [828-1132] |
Synonyms: | JAK2 | JAK2 (aa 828-1132) | JAK2_HUMAN | Tyrosine-protein kinase JAK2 |
Type: | n/a |
Mol. Mass.: | 35579.28 |
Organism: | Homo sapiens (Human) |
Description: | O60674[828-1132] |
Residue: | 305 |
Sequence: | GALGFSGAFEDRDPTQFEERHLKFLQQLGKGNFGSVEMCRYDPLQDNTGEVVAVKKLQHS
TEEHLRDFEREIEILKSLQHDNIVKYKGVCYSAGRRNLKLIMEYLPYGSLRDYLQKHKER
IDHIKLLQYTSQICKGMEYLGTKRYIHRDLATRNILVENENRVKIGDFGLTKVLPQDKEY
YKVKEPGESPIFWYAPESLTESKFSVASDVWSFGVVLYELFTYIEKSKSPPAEFMRMIGN
DKQGQMIVFHLIELLKNNGRLPRPDGCPDEIYMIMTECWNNNVNQRPSFRDLALRVDQIR
DNMAG
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BDBM400285 |
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n/a |
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Name | BDBM400285 |
Synonyms: | US10695337, Example 39 | US11285140, Example 39 | US9999619, Example 40 |
Type | Small organic molecule |
Emp. Form. | C27H27FN8O2 |
Mol. Mass. | 514.5541 |
SMILES | COc1cccc(F)c1C(=O)N1CCC(CC1)N1CC(CC#N)(C1)n1cc(cn1)-c1ncnc2[nH]ccc12 |
Structure |
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