| Reaction Details |
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 | Report a problem with these data |
| Target | Histone-lysine N-methyltransferase SMYD3 |
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| Ligand | BDBM378472 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | SMYD3 Biochemical Assay |
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| IC50 | 15.4±n/a nM |
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| Citation |  Foley, MA; Kuntz, KW; Mills, JE; Mitchell, LH; Munchhof, MJ; Harvey, DM Substituted 1,2,3-triazoles as SMYD inhibitors for treating cancer US Patent US10266526 Publication Date 4/23/2019 |
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| More Info.: | Get all data from this article, Assay Method |
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| Histone-lysine N-methyltransferase SMYD3 |
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| Name: | Histone-lysine N-methyltransferase SMYD3 |
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| Synonyms: | SET and MYND domain-containing protein 3 | SMYD3 | SMYD3_HUMAN | ZMYND1 | ZNFN3A1 | Zinc finger MYND domain-containing protein 1 |
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| Type: | Enzyme |
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| Mol. Mass.: | 49101.22 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Q9H7B4-2 |
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| Residue: | 428 |
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| Sequence: | MEPLKVEKFATAKRGNGLRAVTPLRPGELLFRSDPLAYTVCKGSRGVVCDRCLLGKEKLM
RCSQCRVAKYCSAKCQKKAWPDHKRECKCLKSCKPRYPPDSVRLLGRVVFKLMDGAPSES
EKLYSFYDLESNINKLTEDKKEGLRQLVMTFQHFMREEIQDASQLPPAFDLFEAFAKVIC
NSFTICNAEMQEVGVGLYPSISLLNHSCDPNCSIVFNGPHLLLRAVRDIEVGEELTICYL
DMLMTSEERRKQLRDQYCFECDCFRCQTQDKDADMLTGDEQVWKEVQESLKKIEELKAHW
KWEQVLAMCQAIISSNSERLPDINIYQLKVLDCAMDACINLGLLEEALFYGTRTMEPYRI
FFPGSHPVRGVQVMKVGKLQLHQGMFPQAMKNLRLAFDIMRVTHGREHSLIEDLILLLEE
CDANIRAS
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| BDBM378472 |
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| n/a |
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| Name | BDBM378472 |
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| Synonyms: | N-((2S,4S)-1-((4-aminopiperidin-1-yl)sulfonyl)-2-methylpiperidin-4-yl)-5-ethylisothiazole-3-carboxamide | US10266526, Compound 605 |
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| Type | Small organic molecule |
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| Emp. Form. | C17H29N5O3S2 |
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| Mol. Mass. | 415.574 |
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| SMILES | CCc1cc(ns1)C(=O)N[C@H]1CCN([C@@H](C)C1)S(=O)(=O)N1CCC(N)CC1 |r| |
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| Structure | 
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