Reaction Details |
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Target | N-lysine methyltransferase SMYD2 |
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Ligand | BDBM50550501 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2027562 (CHEMBL4681720) |
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IC50 | 8400±n/a nM |
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Citation | Cowen, SD; Russell, D; Dakin, LA; Chen, H; Larsen, NA; Godin, R; Throner, S; Zheng, X; Molina, A; Wu, J; Cheung, T; Howard, T; Garcia-Arenas, R; Keen, N; Pendleton, CS; Pietenpol, JA; Ferguson, AD Design, Synthesis, and Biological Activity of Substrate Competitive SMYD2 Inhibitors. J Med Chem59:11079-11097 (2016) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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N-lysine methyltransferase SMYD2 |
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Name: | N-lysine methyltransferase SMYD2 |
Synonyms: | HSKM-B | Histone methyltransferase SMYD2 | KMT3C | Lysine N-methyltransferase 3C | N-lysine methyltransferase SMYD2 | SET and MYND domain-containing protein 2 | SET and MYND domain-containing protein 2 (SMYD2) | SMYD2 | SMYD2_HUMAN |
Type: | Enzyme |
Mol. Mass.: | 49689.57 |
Organism: | Homo sapiens (Human) |
Description: | Q9NRG4 |
Residue: | 433 |
Sequence: | MRAEGLGGLERFCSPGKGRGLRALQPFQVGDLLFSCPAYAYVLTVNERGNHCEYCFTRKE
GLSKCGRCKQAFYCNVECQKEDWPMHKLECSPMVVFGENWNPSETVRLTARILAKQKIHP
ERTPSEKLLAVKEFESHLDKLDNEKKDLIQSDIAALHHFYSKHLGFPDNDSLVVLFAQVN
CNGFTIEDEELSHLGSAIFPDVALMNHSCCPNVIVTYKGTLAEVRAVQEIKPGEEVFTSY
IDLLYPTEDRNDRLRDSYFFTCECQECTTKDKDKAKVEIRKLSDPPKAEAIRDMVRYARN
VIEEFRRAKHYKSPSELLEICELSQEKMSSVFEDSNVYMLHMMYQAMGVCLYMQDWEGAL
QYGQKIIKPYSKHYPLYSLNVASMWLKLGRLYMGLEHKAAGEKALKKAIAIMEVAHGKDH
PYISEIKQEIESH
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BDBM50550501 |
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n/a |
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Name | BDBM50550501 |
Synonyms: | CHEMBL4751856 |
Type | Small organic molecule |
Emp. Form. | C22H27N5O |
Mol. Mass. | 377.4827 |
SMILES | CCc1ccccc1-c1cc(C(=O)NCCCN2CCCC2)c2cn[nH]c2n1 |
Structure |
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