Reaction Details |
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Target | Histamine H1 receptor |
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Ligand | BDBM50010859 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2016250 (CHEMBL4669828) |
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Ki | 10.0±n/a nM |
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Citation | Bieszczad, B; Siwek, A; Wilczek, M; Trzybi?ski, D; Wo?niak, K; Sata?a, G; Bojarski, AJ; Mieczkowski, A Synthesis, crystal structure and biological activity of novel analogues of tricyclic drugs. Bioorg Med Chem Lett30:127493 (2020) [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: | H1R | HH1R | HISTAMINE H1 | HRH1 | HRH1_HUMAN |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 55808.72 |
Organism: | Homo sapiens (Human) |
Description: | Cell pellets from SK-N-MC cells transfected with human H1 receptor were used in binding assay. |
Residue: | 487 |
Sequence: | MSLPNSSCLLEDKMCEGNKTTMASPQLMPLVVVLSTICLVTVGLNLLVLYAVRSERKLHT
VGNLYIVSLSVADLIVGAVVMPMNILYLLMSKWSLGRPLCLFWLSMDYVASTASIFSVFI
LCIDRYRSVQQPLRYLKYRTKTRASATILGAWFLSFLWVIPILGWNHFMQQTSVRREDKC
ETDFYDVTWFKVMTAIINFYLPTLLMLWFYAKIYKAVRQHCQHRELINRSLPSFSEIKLR
PENPKGDAKKPGKESPWEVLKRKPKDAGGGSVLKSPSQTPKEMKSPVVFSQEDDREVDKL
YCFPLDIVHMQAAAEGSSRDYVAVNRSHGQLKTDEQGLNTHGASEISEDQMLGDSQSFSR
TDSDTTTETAPGKGKLRSGSNTGLDYIKFTWKRLRSHSRQYVSGLHMNRERKAAKQLGFI
MAAFILCWIPYFIFFMVIAFCKNCCNEHLHMFTIWLGYINSTLNPLIYPLCNENFKKTFK
RILHIRS
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BDBM50010859 |
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n/a |
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Name | BDBM50010859 |
Synonyms: | CHEMBL11 | IMIPRAMINE HYDROCHLORIDE | IMIPRAMINE PAMOATE | Imipramin |
Type | Small organic molecule |
Emp. Form. | C19H24N2 |
Mol. Mass. | 280.4073 |
SMILES | CN(C)CCCN1c2ccccc2CCc2ccccc12 |
Structure |
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