Reaction Details |
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Target | Histamine H1 receptor |
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Ligand | BDBM35922 |
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Substrate/Competitor | BDBM35938 |
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Meas. Tech. | Radioligand Binding Assay |
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Temperature | 298.15±n/a K |
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Ki | 25±n/a nM |
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Comments | extracted |
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Citation | Shah, JR; Mosier, PD; Roth, BL; Kellogg, GE; Westkaemper, RB Synthesis, structure-affinity relationships, and modeling of AMDA analogs at 5-HT2A and H1 receptors: structural factors contributing to selectivity. Bioorg Med Chem17:6496-504 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, 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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BDBM35922 |
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BDBM35938 |
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Name | BDBM35922 |
Synonyms: | (9,10-Dihydro-anthracen-9-ylmethyl)-dimethyl-amine | 1-(9,10-dihydroanthracen-9-yl)-N,N-dimethylmethanamine | 9,10-dihydroanthracene(DHA), 1c | CHEMBL160933 |
Type | Small organic molecule |
Emp. Form. | C17H19N |
Mol. Mass. | 237.3395 |
SMILES | CN(C)CC1c2ccccc2Cc2ccccc12 |
Structure |
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