Reaction Details | |||
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Target | Epidermal growth factor receptor | ||
Ligand | BDBM191622 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | HotSpot kinase assay | ||
IC50 | 22.53±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 | ||
Epidermal growth factor receptor | |||
Name: | Epidermal growth factor receptor | ||
Synonyms: | EGF Receptor Substrate | EGFR | EGFR_HUMAN | ERBB | ERBB1 | Epidermal Growth Factor Receptor Tyrosine Kinase | Epidermal Growth Factor Receptor erbB-1 | Epidermal Growth Factor Receptor, ErbB-1 | Epidermal growth factor receptor (EGFR) | Epidermal growth factor receptor (HER1) | HER1 | Protein-Tyrosine Kinase Erbb-1 | Proto-oncogene c-ErbB-1 | Receptor tyrosine-protein kinase ErbB-1 | Tyrosine-Protein Kinase ErbB-1 | ||
Type: | Receptor Kinase Domain | ||
Mol. Mass.: | 134279.59 | ||
Organism: | Homo sapiens (Human) | ||
Description: | P00533 | ||
Residue: | 1210 | ||
Sequence: |
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BDBM191622 | |||
n/a | |||
Name | BDBM191622 | ||
Synonyms: | US9181263, 18 | ||
Type | Small organic molecule | ||
Emp. Form. | C29H33N7O2 | ||
Mol. Mass. | 511.618 | ||
SMILES | CN(C)C\C=C\C(=O)N[C@H]1CC[C@@H](CC1)n1nc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc12 |r,wU:12.15,wD:9.8,(5.67,1.62,;4.9,.28,;5.67,-1.05,;3.36,.28,;2.59,-1.05,;1.05,-1.05,;.28,-2.39,;1.05,-3.72,;-1.26,-2.39,;-2.03,-1.05,;-1.26,.28,;-2.03,1.62,;-3.57,1.62,;-4.34,.28,;-3.57,-1.05,;-4.34,2.95,;-3.79,4.39,;-4.98,5.36,;-4.98,6.9,;-3.65,7.67,;-3.65,9.21,;-4.98,9.98,;-4.98,11.52,;-3.65,12.29,;-2.32,11.52,;-.98,12.29,;-.98,13.83,;-2.32,14.6,;-3.65,13.83,;-6.32,9.21,;-6.32,7.67,;-6.27,4.52,;-7.76,4.92,;-8.16,6.4,;-8.85,3.83,;-8.45,2.34,;-6.97,1.94,;-5.88,3.03,)| | ||
Structure |