Reaction Details |
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Target | Histone H3.1 |
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Ligand | BDBM50248522 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Histone H3 Acetylation Assay |
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EC50 | 500±n/a nM |
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Citation | Chen, D; Song, HY; Sun, ET; Yu, N; Zou, Y Benzimidazole derivatives: preparation and pharmaceutical applications US Patent US10201527 Publication Date 2/12/2019 |
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More Info.: | Get all data from this article, Assay Method |
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Histone H3.1 |
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Name: | Histone H3.1 |
Synonyms: | H31_HUMAN | H3C1 | H3FA | H3FB | H3FC HIST1H3C | H3FD | H3FF | H3FH | H3FI | H3FJ | H3FK | H3FL | HIST1H3A | HIST1H3B | HIST1H3D | HIST1H3E | HIST1H3F | HIST1H3G | HIST1H3H | HIST1H3I | HIST1H3J |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 15425.07 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 136 |
Sequence: | MARTKQTARKSTGGKAPRKQLATKAARKSAPATGGVKKPHRYRPGTVALREIRRYQKSTE
LLIRKLPFQRLVREIAQDFKTDLRFQSSAVMALQEACEAYLVGLFEDTNLCAIHAKRVTI
MPKDIQLARRIRGERA
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BDBM50248522 |
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n/a |
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Name | BDBM50248522 |
Synonyms: | CHEMBL489332 | N-hydroxy-3-(2-phenethyl-1-(2-(piperidin-1-yl)ethyl)-1H-benzo[d]imidazol-5-yl)acrylamide | US10201527, Compound 67 | US10736881, Compound 67 | US8551988, 67 |
Type | Small organic molecule |
Emp. Form. | C25H30N4O2 |
Mol. Mass. | 418.5313 |
SMILES | ONC(=O)\C=C\c1ccc2n(CCN3CCCCC3)c(CCc3ccccc3)nc2c1 |
Structure |
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