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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | Histone-lysine N-methyltransferase SMYD3 | ||
| Ligand | BDBM293376 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | SMYD3 Biochemical Assay | ||
| IC50 | 9690±n/a nM | ||
| Citation |  Foley, MA; Kuntz, KW; Mitchell, LH; Munchhof, MJ Substituted isoxazoles for treating cancer US Patent US10106510 Publication Date 10/23/2018 | ||
| More Info.: | Get all data from this article, Assay Method | ||
| Histone-lysine N-methyltransferase SMYD3 | |||
| Name: | Histone-lysine N-methyltransferase SMYD3 | ||
| Synonyms: | SET and MYND domain-containing protein 3 | SMYD3 | SMYD3_HUMAN | ZMYND1 | ZNFN3A1 | Zinc finger MYND domain-containing protein 1 | ||
| Type: | Enzyme | ||
| Mol. Mass.: | 49101.22 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | Q9H7B4-2 | ||
| Residue: | 428 | ||
| Sequence: |
| ||
| BDBM293376 | |||
| n/a | |||
| Name | BDBM293376 | ||
| Synonyms: | N-((1R,4r)-4-((R)-3- aminobutanamido) cyclohexyl)-5- cyclopropyl-N-(2- methoxyethyl)isoxazole- 3-carboxamide | US10106510, Compound 40 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C20H32N4O4 | ||
| Mol. Mass. | 392.4925 | ||
| SMILES | COCCN([C@H]1CC[C@@H](CC1)NC(=O)C[C@@H](C)N)C(=O)c1cc(on1)C1CC1 |r,wU:5.4,wD:8.11,15.17,(6.73,-3.08,;5.4,-3.85,;4.07,-3.08,;2.73,-3.85,;1.4,-3.08,;1.4,-1.54,;.07,-.77,;.07,.77,;1.4,1.54,;2.73,.77,;2.73,-.77,;1.4,3.08,;2.73,3.85,;2.73,5.39,;4.07,3.08,;5.4,3.85,;6.73,3.08,;5.4,5.39,;.07,-3.85,;.07,-5.39,;-1.27,-3.08,;-2.51,-3.99,;-3.76,-3.08,;-3.28,-1.62,;-1.74,-1.62,;-5.25,-3.48,;-6.73,-3.08,;-6.34,-4.57,)| | ||
| Structure | 
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