Reaction Details | |||
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Target | Histone-lysine N-methyltransferase EZH2 [A687V] | ||
Ligand | BDBM190211 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Inhibition Assay | ||
IC50 | 1.7±n/a nM | ||
Citation | Kuntz, KW; Knutson, SK; Wigle, TJ Inhibitors of human EZH2, and methods of use thereof US Patent US9175331 Publication Date 11/3/2015 | ||
More Info.: | Get all data from this article, Assay Method | ||
Histone-lysine N-methyltransferase EZH2 [A687V] | |||
Name: | Histone-lysine N-methyltransferase EZH2 [A687V] | ||
Synonyms: | EZH2 | EZH2_HUMAN | Histone-lysine N-methyltransferase EZH2 (A687V) | KMT6 | ||
Type: | Protein | ||
Mol. Mass.: | 85395.90 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Q15910[A687V] | ||
Residue: | 746 | ||
Sequence: |
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BDBM190211 | |||
n/a | |||
Name | BDBM190211 | ||
Synonyms: | EPZ008990 | US9175331, 47 | ||
Type | Small organic molecule | ||
Emp. Form. | C28H39ClN4O3 | ||
Mol. Mass. | 515.087 | ||
SMILES | CCN([C@H]1CC[C@@H](CC1)N(C)C1COC1)c1cc(Cl)cc(C(=O)NCc2c(C)cc(C)[nH]c2=O)c1C |r,wU:3.2,wD:6.9,(-2.67,-3.15,;-1.33,-3.92,;,-3.15,;1.33,-3.92,;2.67,-3.15,;4,-3.92,;4,-5.46,;2.67,-6.23,;1.33,-5.46,;5.33,-6.23,;6.67,-5.46,;5.33,-7.77,;4.25,-8.85,;5.33,-9.94,;6.42,-8.85,;,-1.61,;1.33,-.84,;1.33,.7,;2.67,1.47,;,1.47,;-1.33,.7,;-2.67,1.47,;-4,.7,;-2.67,3.01,;-4,3.78,;-4,5.32,;-5.33,6.09,;-6.67,5.32,;-5.33,7.63,;-4,8.4,;-4,9.94,;-2.67,7.63,;-2.67,6.09,;-1.33,5.32,;-1.33,-.84,;-2.67,-1.61,)| | ||
Structure |