Reaction Details | |||
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Target | Tyrosine-protein kinase Lck | ||
Ligand | BDBM191614 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | HotSpot kinase assay | ||
IC50 | 0.88±n/a nM | ||
Citation | Honigberg, L; Verner, E; Buggy, JJ; Loury, D; Chen, W Inhibitors of bruton's tyrosine kinase US Patent US9181263 Publication Date 11/10/2015 | ||
More Info.: | Get all data from this article, Assay Method | ||
Tyrosine-protein kinase Lck | |||
Name: | Tyrosine-protein kinase Lck | ||
Synonyms: | 2.7.10.2 | LCK | LCK_HUMAN | LSK | Leukocyte C-terminal Src kinase | Lymphocyte cell-specific protein-tyrosine kinase | Lymphocyte-specific protein tyrosine kinase | P56-LCK | Protein YT16 | Proto-oncogene Lck | Proto-oncogene tyrosine-protein kinase LCK | Src/Lck kinase | T cell-specific protein-tyrosine kinase | ||
Type: | n/a | ||
Mol. Mass.: | 57987.83 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P06239 | ||
Residue: | 509 | ||
Sequence: |
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BDBM191614 | |||
n/a | |||
Name | BDBM191614 | ||
Synonyms: | US9181263, 10 | US9278100, 10 | ||
Type | Small organic molecule | ||
Emp. Form. | C26H26N6O2 | ||
Mol. Mass. | 454.5236 | ||
SMILES | Nc1ncnc2n(nc(-c3ccc(Oc4ccccc4)cc3)c12)[C@H]1CC[C@@H](CC1)NC(=O)C=C |r,wU:23.26,wD:26.33,(-8.87,3.22,;-8.1,1.89,;-8.87,.55,;-8.1,-.78,;-6.56,-.78,;-5.79,.55,;-4.28,.87,;-4.12,2.4,;-5.53,3.03,;-5.93,4.52,;-4.84,5.61,;-5.24,7.1,;-6.72,7.49,;-7.12,8.98,;-6.03,10.07,;-4.55,9.67,;-3.46,10.76,;-3.86,12.25,;-5.34,12.65,;-6.43,11.56,;-7.81,6.4,;-7.41,4.92,;-6.56,1.89,;-2.95,.1,;-1.62,.87,;-.28,.1,;-.28,-1.44,;-1.62,-2.21,;-2.95,-1.44,;1.05,-2.21,;2.39,-1.44,;2.39,.1,;3.72,-2.21,;5.05,-1.44,)| | ||
Structure |