Reaction Details |
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Target | 5-hydroxytryptamine receptor 4 |
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Ligand | BDBM327445 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Competition Assay |
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Ki | 8.90±n/a nM |
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Citation | Dallemagne, P; Rochais, C; Lecoutey, C; Boulouard, M; Freret, T Acetylcholinesterase inhibitors and promnesiant serotonin 5-HT4 receptor agonists, their methods of preparation and the pharmaceutical compositions containing the same US Patent US9663465 Publication Date 5/30/2017 |
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More Info.: | Get all data from this article, Assay Method |
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5-hydroxytryptamine receptor 4 |
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Name: | 5-hydroxytryptamine receptor 4 |
Synonyms: | 5-HT-4 | 5-HT4 | 5-HT4S | 5-HT4a | 5-HT4b | 5-HT4c | 5-HT4d | 5-HT4hb | 5-hydroxytryptamine receptor 4 | 5-hydroxytryptamine receptor 4 (5-HT4) | 5HT4R_HUMAN | HTR4 | Serotonin (5-HT) receptor | Serotonin (5-HT3) receptor | Serotonin 4 (5-HT4) receptor | Serotonin Receptor 4 |
Type: | Enzyme |
Mol. Mass.: | 43767.54 |
Organism: | Homo sapiens (Human) |
Description: | Q13639 |
Residue: | 388 |
Sequence: | MDKLDANVSSEEGFGSVEKVVLLTFLSTVILMAILGNLLVMVAVCWDRQLRKIKTNYFIV
SLAFADLLVSVLVMPFGAIELVQDIWIYGEVFCLVRTSLDVLLTTASIFHLCCISLDRYY
AICCQPLVYRNKMTPLRIALMLGGCWVIPTFISFLPIMQGWNNIGIIDLIEKRKFNQNSN
STYCVFMVNKPYAITCSVVAFYIPFLLMVLAYYRIYVTAKEHAHQIQMLQRAGASSESRP
QSADQHSTHRMRTETKAAKTLCIIMGCFCLCWAPFFVTNIVDPFIDYTVPGQVWTAFLWL
GYINSGLNPFLYAFLNKSFRRAFLIILCCDDERYRRPSILGQTVPCSTTTINGSTHVLRD
AVECGGQWESQCHPPATSPLVAAQPSDT
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BDBM327445 |
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n/a |
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Name | BDBM327445 |
Synonyms: | 1-(4-amino-5-bromo-2-methoxyphenyl)-3-[1-butyl-4-piperidyl]propan-1-one | US9663465, 2 |
Type | Small organic molecule |
Emp. Form. | C19H28BrNO2 |
Mol. Mass. | 382.335 |
SMILES | CCCCN1CCC(CCC(=O)c2cc(Br)ccc2OC)CC1 |
Structure |
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