| Reaction Details |
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 | Report a problem with these data |
| Target | 5-hydroxytryptamine receptor 2B |
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| Ligand | BDBM50404644 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_2900 (CHEMBL617617) |
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| Kd | 36.31±n/a nM |
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| Citation |  Glennon, RA; Liebowitz, SM; Leming-Doot, D; Rosecrans, JA Demethyl analogues of psychoactive methoxyphenalkylamines: synthesis and serotonin receptor affinities. J Med Chem23:990-4 (1980) [PubMed] |
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| More Info.: | Get all data from this article, Assay Method |
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| 5-hydroxytryptamine receptor 2B |
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| Name: | 5-hydroxytryptamine receptor 2B |
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| Synonyms: | 5-HT2B | 5-hydroxytryptamine receptor 2B | 5HT2B_RAT | Htr2b | Serotonin 2b (5-HT2b) receptor | Serotonin receptor 2a and 2b (5HT2A and 5HT2B) | Srl |
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| Type: | Enzyme Catalytic Domain |
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| Mol. Mass.: | 53668.47 |
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| Organism: | RAT |
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| Description: | 5-HT2B HTR2B RAT::P30994 |
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| Residue: | 479 |
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| Sequence: | MASSYKMSEQSTISEHILQKTCDHLILTDRSGLKAESAAEEMKQTAENQGNTVHWAALLI
FAVIIPTIGGNILVILAVSLEKRLQYATNYFLMSLAVADLLVGLFVMPIALLTIMFEATW
PLPLALCPAWLFLDVLFSTASIMHLCAISLDRYIAIKKPIQANQCNSRTTAFVKITVVWL
ISIGIAIPVPIKGIEADVVNAHNITCELTKDRFGSFMLFGSLAAFFAPLTIMIVTYFLTI
HALRKKAYLVRNRPPQRLTRWTVSTVLQREDSSFSSPEKMVMLDGSHKDKILPNSTDETL
MRRMSSAGKKPAQTISNEQRASKVLGIVFLFFLLMWCPFFITNVTLALCDSCNQTTLKTL
LQIFVWVGYVSSGVNPLIYTLFNKTFREAFGRYITCNYQATKSVKVLRKCSSTLYFGNSM
VENSKFFTKHGIRNGINPAMYQSPVRLRSSTIQSSSIILLNTFLTENDGDKVEDQVSYI
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| BDBM50404644 |
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| n/a |
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| Name | BDBM50404644 |
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| Synonyms: | CHEMBL174380 |
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| Type | Small organic molecule |
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| Emp. Form. | C11H17NO2 |
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| Mol. Mass. | 195.2582 |
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| SMILES | COc1cc(CC(C)N)c(O)cc1C |
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| Structure | 
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