| Reaction Details |
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 | Report a problem with these data |
| Target | Histone H1.0 |
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| Ligand | BDBM21398 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | Binding Assay |
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| Ki | 780±0.0 nM |
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| Citation |  Mates, S; Fienberg, A; Wennogle, L Methods and compositions for sleep disorders and other disorders US Patent US8598119 Publication Date 12/3/2013 |
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| More Info.: | Get all data from this article, Assay Method |
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| Histone H1.0 |
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| Name: | Histone H1.0 |
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| Synonyms: | H1-0 | H10_HUMAN | H1F0 | H1FV | Histone H1 |
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| Type: | Cell-surface receptors |
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| Mol. Mass.: | 20917.09 |
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| Organism: | Homo sapiens (Human) |
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| Description: | P07305 |
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| Residue: | 194 |
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| Sequence: | MTENSTSAPAAKPKRAKASKKSTDHPKYSDMIVAAIQAEKNRAGSSRQSIQKYIKSHYKV
GENADSQIKLSIKRLVTTGVLKQTKGVGASGSFRLAKSDEPKKSVAFKKTKKEIKKVATP
KKASKPKKAASKAPTKKPKATPVKKAKKKLAATPKKAKKPKTVKAKPVKASKPKKAKPVK
PKAKSSAKRAGKKK
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|
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| BDBM21398 |
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| n/a |
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| Name | BDBM21398 |
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| Synonyms: | 4-[4-(4-Chloro-phenyl)-4-hydroxy-piperidin-1-yl]-1-(4-fluoro-phenyl)-butan-1-one;propionate(HCl) | 4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-1-(4-fluorophenyl)butan-1-one | CHEMBL54 | CHEMBL545608 | Haloperidol | Haloperidol, 1 |
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| Type | Small organic molecule |
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| Emp. Form. | C21H23ClFNO2 |
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| Mol. Mass. | 375.864 |
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| SMILES | OC1(CCN(CCCC(=O)c2ccc(F)cc2)CC1)c1ccc(Cl)cc1 |
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| Structure | 
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