Reaction Details |
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Target | Histone-lysine N-methyltransferase SUV39H2 |
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Ligand | BDBM422846 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Suv 39H2 Assay |
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IC50 | 4.35±n/a nM |
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Citation | Matsuo, Y; Hisada, S; Nakamura, Y; Chakrabarti, A; Rawat, M; Rai, S; Satyanarayana, AV; Duan, Z; Talukdar, A; Ravula, S; Decornez, H Bicyclic compound and use thereof for inhibiting SUV39H2 US Patent US10508109 Publication Date 12/17/2019 |
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More Info.: | Get all data from this article, Assay Method |
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Histone-lysine N-methyltransferase SUV39H2 |
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Name: | Histone-lysine N-methyltransferase SUV39H2 |
Synonyms: | H3-K9-HMTase 2 | Histone H3-K9 methyltransferase 2 | Histone-lysine N-methyltransferase SUV39H2 | Histone-lysine N-methyltransferase SUV39H2 (Suv39H2) | KMT1B | Lysine N-methyltransferase 1B | SUV39H2 | SUV92_HUMAN | Su(var)3-9 homolog 2 | Suppressor of variegation 3-9 homolog 2 |
Type: | Enzyme |
Mol. Mass.: | 46692.47 |
Organism: | Homo sapiens (Human) |
Description: | Q9H5I1 |
Residue: | 410 |
Sequence: | MAAVGAEARGAWCVPCLVSLDTLQELCRKEKLTCKSIGITKRNLNNYEVEYLCDYKVVKD
MEYYLVKWKGWPDSTNTWEPLQNLKCPLLLQQFSNDKHNYLSQVKKGKAITPKDNNKTLK
PAIAEYIVKKAKQRIALQRWQDELNRRKNHKGMIFVENTVDLEGPPSDFYYINEYKPAPG
ISLVNEATFGCSCTDCFFQKCCPAEAGVLLAYNKNQQIKIPPGTPIYECNSRCQCGPDCP
NRIVQKGTQYSLCIFRTSNGRGWGVKTLVKIKRMSFVMEYVGEVITSEEAERRGQFYDNK
GITYLFDLDYESDEFTVDAARYGNVSHFVNHSCDPNLQVFNVFIDNLDTRLPRIALFSTR
TINAGEELTFDYQMKGSGDISSDSIDHSPAKKRVRTVCKCGAVTCRGYLN
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BDBM422846 |
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n/a |
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Name | BDBM422846 |
Synonyms: | N-(1-(2-(5-chloro-2,4- dimethoxyphenyl)imidazo[1,2- a]pyridin-7-yl)pyrrolidin-3- yl)acetamide | US10508109, Example 37 |
Type | Small organic molecule |
Emp. Form. | C21H23ClN4O3 |
Mol. Mass. | 414.885 |
SMILES | COc1cc(CO)c(cc1Cl)-c1cn2ccc(cc2n1)N1CCC(C1)NC(C)=O |
Structure |
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