Reaction Details |
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Target | Histamine H1 receptor |
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Ligand | BDBM50313618 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_614259 (CHEMBL1106922) |
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Ki | 1995.26±n/a nM |
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Citation | Holmes, IP; Blunt, RJ; Lorthioir, OE; Blowers, SM; Gribble, A; Payne, AH; Stansfield, IG; Wood, M; Woollard, PM; Reavill, C; Howes, CM; Micheli, F; Di Fabio, R; Donati, D; Terreni, S; Hamprecht, D; Arista, L; Worby, A; Watson, SP The identification of a selective dopamine D2 partial agonist, D3 antagonist displaying high levels of brain exposure. Bioorg Med Chem Lett20:2013-6 (2010) [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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BDBM50313618 |
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n/a |
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Name | BDBM50313618 |
Synonyms: | 1-(3-chlorophenyl)-3-(piperidin-2-ylmethyl)imidazolidin-2-one | CHEMBL1085672 |
Type | Small organic molecule |
Emp. Form. | C15H20ClN3O |
Mol. Mass. | 293.792 |
SMILES | Clc1cccc(c1)N1CCN(CC2CCCCN2)C1=O |
Structure |
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