Reaction Details |
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Target | Histamine H1 receptor |
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Ligand | BDBM50265376 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_558570 (CHEMBL959899) |
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Ki | 15±n/a nM |
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Citation | Butini, S; Gemma, S; Campiani, G; Franceschini, S; Trotta, F; Borriello, M; Ceres, N; Ros, S; Coccone, SS; Bernetti, M; De Angelis, M; Brindisi, M; Nacci, V; Fiorini, I; Novellino, E; Cagnotto, A; Mennini, T; Sandager-Nielsen, K; Andreasen, JT; Scheel-Kruger, J; Mikkelsen, JD; Fattorusso, C Discovery of a new class of potential multifunctional atypical antipsychotic agents targeting dopamine D3 and serotonin 5-HT1A and 5-HT2A receptors: design, synthesis, and effects on behavior. J Med Chem52:151-69 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Histamine H1 receptor |
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Name: | Histamine H1 receptor |
Synonyms: | HISTAMINE H1 | HRH1 | HRH1_CAVPO |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 55641.53 |
Organism: | Cavia porcellus (domestic guinea pig) |
Description: | Guinea pig cerebellum was used in binding assay. |
Residue: | 488 |
Sequence: | MSFLPGMTPVTLSNFSWALEDRMLEGNSTTTPTRQLMPLVVVLSSVSLVTVALNLLVLYA
VRSERKLHTVGNLYIVSLSVADLIVGAVVMPMSILYLHRSAWILGRPLCLFWLSMDYVAS
TASIFSVFILCIDRYRSVQQPLRYLRYRTKTRASATILGAWLLSFLWVIPILGWHHFMAP
TSEPREKKCETDFYDVTWFKVMTAIINFYLPTLLMLWFYIRIYKAVRRHCQHRQLINSSL
PSFSEMKLKLENAKVDTRRMGKESPWEDPKRCSKDASGVHTPMPSSQHLVDMPCAAVLSE
DEGGEVGTRQMPMLAVGDGRCCEALNHMHSQLELSGQSRATHSISARPEEWTVVDGQSFP
ITDSDTSTEAAPMGGQPRSGSNSGLDYIKFTWRRLRSHSRQYTSGLHLNRERKAAKQLGC
IMAAFILCWIPYFVFFMVIAFCKSCSNEPVHMFTIWLGYLNSTLNPLIYPLCNENFRKTF
KRILRIPP
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BDBM50265376 |
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n/a |
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Name | BDBM50265376 |
Synonyms: | CHEMBL496739 | N-(4-(4-(m-Tolyl)piperazin-1-yl)butyl)benzo[b]furan-2-carboxamide | N-(4-(4-m-tolylpiperazin-1-yl)butyl)benzofuran-2-carboxamide |
Type | Small organic molecule |
Emp. Form. | C24H29N3O2 |
Mol. Mass. | 391.506 |
SMILES | Cc1cccc(c1)N1CCN(CCCCNC(=O)c2cc3ccccc3o2)CC1 |
Structure |
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