Reaction Details |
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Target | 5-hydroxytryptamine receptor 4 |
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Ligand | BDBM85026 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1460447 (CHEMBL3367331) |
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Ki | 0.398107±n/a nM |
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Citation | Brudeli, B; Navaratnarajah, M; Andressen, KW; Manfra, O; Moltzau, LR; Nilsen, NO; Levy, FO; Klaveness, J Discovery and pharmacological profile of new hydrophilic 5-HT(4) receptor antagonists. Bioorg Med Chem Lett24:4598-602 (2014) [PubMed] Article |
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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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BDBM85026 |
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n/a |
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Name | BDBM85026 |
Synonyms: | N-(1-Butylpiperidine-4-ylmethyl)-1,2-(trimethyleneoxy)-1H-indole-3-carboxamide | SB 207266 | SB-207266 |
Type | Small organic molecule |
Emp. Form. | C22H31N3O2 |
Mol. Mass. | 369.5004 |
SMILES | CCCCN1CCC(CNC(=O)c2c3OCCCn3c3ccccc23)CC1 |
Structure |
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