Reaction Details |
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Target | 5-hydroxytryptamine receptor 2B |
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Ligand | BDBM50541196 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1983949 (CHEMBL4617355) |
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Ki | 21±n/a nM |
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Citation | Ren, A; Zhu, X; Feichtinger, K; Lehman, J; Kasem, M; Schrader, TO; Wong, A; Dang, H; Le, M; Frazer, J; Unett, DJ; Grottick, AJ; Whelan, KT; Morgan, ME; Sage, CR; Semple, G Discovery of a lead series of potent benzodiazepine 5-HT Bioorg Med Chem Lett30:0 (2020) [PubMed] Article |
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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 |
Synonyms: | 5-HT-2B | 5-HT2B | 5-hydroxytryptamine (serotonin) receptor 2B [Homo sapiens] | 5-hydroxytryptamine receptor 2B (5-HT2B) | 5-hydroxytryptamine receptor 2C (5HT2C) | 5HT2B_HUMAN | HTR2B | Serotonin (5-HT3) receptor | Serotonin 2b (5-HT2b) receptor | Serotonin Receptor 2B |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 54312.47 |
Organism: | Homo sapiens (Human) |
Description: | Receptor binding assays were performed using human clone stably expressed in CHO cells. |
Residue: | 481 |
Sequence: | MALSYRVSELQSTIPEHILQSTFVHVISSNWSGLQTESIPEEMKQIVEEQGNKLHWAALL
ILMVIIPTIGGNTLVILAVSLEKKLQYATNYFLMSLAVADLLVGLFVMPIALLTIMFEAM
WPLPLVLCPAWLFLDVLFSTASIMHLCAISVDRYIAIKKPIQANQYNSRATAFIKITVVW
LISIGIAIPVPIKGIETDVDNPNNITCVLTKERFGDFMLFGSLAAFFTPLAIMIVTYFLT
IHALQKKAYLVKNKPPQRLTWLTVSTVFQRDETPCSSPEKVAMLDGSRKDKALPNSGDET
LMRRTSTIGKKSVQTISNEQRASKVLGIVFFLFLLMWCPFFITNITLVLCDSCNQTTLQM
LLEIFVWIGYVSSGVNPLVYTLFNKTFRDAFGRYITCNYRATKSVKTLRKRSSKIYFRNP
MAENSKFFKKHGIRNGINPAMYQSPMRLRSSTIQSSSIILLDTLLLTENEGDKTEEQVSY
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BDBM50541196 |
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n/a |
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Name | BDBM50541196 |
Synonyms: | CHEMBL4639090 |
Type | Small organic molecule |
Emp. Form. | C12H15BrN2 |
Mol. Mass. | 267.165 |
SMILES | CC1CN2CCNCc3ccc(Br)c1c23 |
Structure |
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