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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Tyrosine-protein kinase JAK3 [512-1124] | ||
| Ligand | BDBM493259 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | Enzymatic Inhibition Assay | ||
| IC50 | 16.6±n/a nM | ||
| Citation |  Bacani, GM; Chai, W; Koudriakova, T; Krawczuk, PJ; Kreutter, KD; Leonard, K; Rizzolio, MC; Seierstad, M; Smith, RC; Tichenor, MS; Venable, JD; Wang, A Imidazopyrrolopyridine as inhibitors of the JAK family of kinases US Patent US10981911 Publication Date 4/20/2021 | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Tyrosine-protein kinase JAK3 [512-1124] | |||
| Name: | Tyrosine-protein kinase JAK3 [512-1124] | ||
| Synonyms: | JAK3 | JAK3 (aa 512-1124) | JAK3_HUMAN | ||
| Type: | Protein | ||
| Mol. Mass.: | 68951.94 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | P52333[512-1124] | ||
| Residue: | 613 | ||
| Sequence: |
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| BDBM493259 | |||
| n/a | |||
| Name | BDBM493259 | ||
| Synonyms: | 2-(8-bromo-1-((1r,4r)-4-(cyanomethyl)cyclohexyl)-1,6-dihydroimidazo[4,5-d]pyrrolo[2,3-b]pyridin-2-yl)-N-(2-hydroxy-2-methylpropyl)acetamide | US10981911, Example 189 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C22H27BrN6O2 | ||
| Mol. Mass. | 487.393 | ||
| SMILES | CC(C)(O)CNC(=O)Cc1nc2cnc3[nH]cc(Br)c3c2n1[C@H]1CC[C@H](CC#N)CC1 |r,wU:25.28,wD:22.24,(-7.9,3.71,;-6.36,3.71,;-5.59,5.04,;-7.13,5.04,;-5.59,2.37,;-4.05,2.37,;-3.28,1.04,;-4.05,-.29,;-1.74,1.04,;-.97,-.29,;-1.59,-1.7,;-.45,-2.73,;-.45,-4.27,;.89,-5.04,;2.22,-4.27,;3.68,-4.75,;4.59,-3.5,;3.68,-2.26,;4.45,-.92,;2.22,-2.73,;.89,-1.96,;.57,-.45,;1.65,.63,;3.14,.24,;4.23,1.32,;3.83,2.81,;4.92,3.9,;6.41,3.5,;7.9,3.1,;2.34,3.21,;1.26,2.12,)| | ||
| Structure | 
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