Reaction Details |
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Target | 5-hydroxytryptamine receptor 4 |
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Ligand | BDBM50398966 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_875039 (CHEMBL2184357) |
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Ki | 19.95±n/a nM |
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Citation | Furlotti, G; Alisi, MA; Apicella, C; Capezzone de Joannon, A; Cazzolla, N; Costi, R; Cuzzucoli Crucitti, G; Garrone, B; Iacovo, A; Magarò, G; Mangano, G; Miele, G; Ombrato, R; Pescatori, L; Polenzani, L; Rosi, F; Vitiello, M; Di Santo, R Discovery and pharmacological profile of new 1H-indazole-3-carboxamide and 2H-pyrrolo[3,4-c]quinoline derivatives as selective serotonin 4 receptor ligands. J Med Chem55:9446-66 (2012) [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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BDBM50398966 |
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n/a |
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Name | BDBM50398966 |
Synonyms: | CHEMBL2179671 |
Type | Small organic molecule |
Emp. Form. | C28H33N3O2 |
Mol. Mass. | 443.5805 |
SMILES | COCc1ccc(CCN2CCC(COc3nc4ccccc4c4cn(C)cc34)CC2)cc1 |
Structure |
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