Reaction Details | |||
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Target | Tyrosine-protein kinase JAK1 | ||
Ligand | BDBM50391985 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_851246 (CHEMBL2155758) | ||
Ki | 5.9±n/a nM | ||
Citation | Kulagowski, JJ; Blair, W; Bull, RJ; Chang, C; Deshmukh, G; Dyke, HJ; Eigenbrot, C; Ghilardi, N; Gibbons, P; Harrison, TK; Hewitt, PR; Liimatta, M; Hurley, CA; Johnson, A; Johnson, T; Kenny, JR; Bir Kohli, P; Maxey, RJ; Mendonca, R; Mortara, K; Murray, J; Narukulla, R; Shia, S; Steffek, M; Ubhayakar, S; Ultsch, M; van Abbema, A; Ward, SI; Waszkowycz, B; Zak, M Identification of imidazo-pyrrolopyridines as novel and potent JAK1 inhibitors. J Med Chem55:5901-21 (2012) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Tyrosine-protein kinase JAK1 | |||
Name: | Tyrosine-protein kinase JAK1 | ||
Synonyms: | JAK-1 | JAK1 | JAK1A | JAK1B | JAK1_HUMAN | Janus kinase 1 | Janus kinase 1 (JAK1) | Janus kinase 1 JAK1 | ||
Type: | Protein | ||
Mol. Mass.: | 133293.73 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P23458 | ||
Residue: | 1154 | ||
Sequence: |
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BDBM50391985 | |||
n/a | |||
Name | BDBM50391985 | ||
Synonyms: | CHEMBL2152421 | ||
Type | Small organic molecule | ||
Emp. Form. | C22H22N6 | ||
Mol. Mass. | 370.4503 | ||
SMILES | N#Cc1cccc(CN[C@H]2CC[C@@H](CC2)n2cnc3cnc4[nH]ccc4c23)c1 |r,wU:9.8,wD:12.15,(1.74,-19.09,;2.51,-20.43,;3.28,-21.75,;4.82,-21.76,;5.59,-23.1,;4.81,-24.43,;3.27,-24.41,;2.49,-25.73,;.95,-25.72,;.17,-27.05,;.93,-28.39,;.16,-29.72,;-1.38,-29.71,;-2.15,-28.38,;-1.37,-27.04,;-2.15,-31.04,;-3.68,-30.88,;-4.3,-32.28,;-3.16,-33.3,;-3.16,-34.85,;-1.83,-35.62,;-.5,-34.84,;.97,-35.32,;1.88,-34.07,;.97,-32.82,;-.5,-33.3,;-1.84,-32.54,;2.5,-23.08,)| | ||
Structure |