Reaction Details | |||
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Target | Tyrosine-protein kinase SYK | ||
Ligand | BDBM182068 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Homogeneous Time-Resolved Fluorescence (HTRF) Assay | ||
pH | 7.5±n/a | ||
Temperature | 298.15±n/a K | ||
IC50 | 1±n/a nM | ||
Comments | extracted | ||
Citation | Deschenes, D; Altman, MD; Ellis, JM; Fischer, C; Haidle, AM; Kattar, SD; Northrup, AB; Schell, AJ; Smith, GF; Taoka, BM; Bienstock, C; Di Francesco, ME; Donofrio, A; Peterson, S; Spencer, KB; Jewell, JP; Ali, A; Bennett, DJ; Dang, Q; Wai, J Bipyridylaminopyridines as Syk inhibitors US Patent US9145391 Publication Date 9/29/2015 | ||
More Info.: | Get all data from this article, Assay Method | ||
Tyrosine-protein kinase SYK | |||
Name: | Tyrosine-protein kinase SYK | ||
Synonyms: | KSYK_HUMAN | SYK | Spleen Tyrosine Kinase | Spleen tyrosine kinase (SYK) | Tyrosine-protein kinase SYK (Syk) | ||
Type: | Enzyme | ||
Mol. Mass.: | 72079.99 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P43405 | ||
Residue: | 635 | ||
Sequence: |
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BDBM182068 | |||
n/a | |||
Name | BDBM182068 | ||
Synonyms: | US9145391, 1-36 | ||
Type | Small organic molecule | ||
Emp. Form. | C28H30F2N4O3 | ||
Mol. Mass. | 508.5596 | ||
SMILES | CC(=O)C(C)(C1CCC(CC1)C(O)=O)c1ccc(cn1)-c1cc(C)cc(Nc2cc(ccn2)C(F)F)n1 |(2.04,-3.23,;1.27,-1.9,;2.04,-.56,;-.27,-1.9,;-1.81,-1.9,;-.27,-.36,;1.06,.41,;1.06,1.95,;-.27,2.72,;-1.6,1.95,;-1.6,.41,;-.27,4.26,;1.06,5.03,;-1.6,5.03,;-.27,-3.44,;1.06,-4.21,;1.06,-5.75,;-.27,-6.52,;-1.6,-5.75,;-1.6,-4.21,;-.27,-8.06,;1.06,-8.83,;1.06,-10.37,;2.4,-11.14,;-.27,-11.14,;-1.6,-10.37,;-2.94,-11.14,;-4.27,-10.37,;-4.27,-8.83,;-5.6,-8.06,;-6.94,-8.83,;-6.94,-10.37,;-5.6,-11.14,;-5.6,-6.52,;-6.94,-5.75,;-4.23,-5.71,;-1.6,-8.83,)| | ||
Structure |