Reaction Details |
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Target | Histamine H4 receptor |
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Ligand | BDBM50418061 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_735234 (CHEMBL1694496) |
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Ki | 89.13±n/a nM |
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Citation | Wijtmans, M; de Graaf, C; de Kloe, G; Istyastono, EP; Smit, J; Lim, H; Boonnak, R; Nijmeijer, S; Smits, RA; Jongejan, A; Zuiderveld, O; de Esch, IJ; Leurs, R Triazole ligands reveal distinct molecular features that induce histamine H4 receptor affinity and subtly govern H4/H3 subtype selectivity. J Med Chem54:1693-703 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Histamine H4 receptor |
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Name: | Histamine H4 receptor |
Synonyms: | AXOR35 | G-protein coupled receptor 105 | GPCR105 | GPRv53 | HH4R | HISTAMINE H4 | HRH4 | HRH4_HUMAN | Histamine H4 receptor | Histamine H4 receptor (H4R) | Histamine receptor (H3 and H4) | Pfi-013 | SP9144 |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 44517.02 |
Organism: | Homo sapiens (Human) |
Description: | Binding assays were using CHO cells stably expressing hH4R receptors. |
Residue: | 390 |
Sequence: | MPDTNSTINLSLSTRVTLAFFMSLVAFAIMLGNALVILAFVVDKNLRHRSSYFFLNLAIS
DFFVGVISIPLYIPHTLFEWDFGKEICVFWLTTDYLLCTASVYNIVLISYDRYLSVSNAV
SYRTQHTGVLKIVTLMVAVWVLAFLVNGPMILVSESWKDEGSECEPGFFSEWYILAITSF
LEFVIPVILVAYFNMNIYWSLWKRDHLSRCQSHPGLTAVSSNICGHSFRGRLSSRRSLSA
STEVPASFHSERQRRKSSLMFSSRTKMNSNTIASKMGSFSQSDSVALHQREHVELLRARR
LAKSLAILLGVFAVCWAPYSLFTIVLSFYSSATGPKSVWYRIAFWLQWFNSFVNPLLYPL
CHKRFQKAFLKIFCIKKQPLPSQHSRSVSS
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BDBM50418061 |
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n/a |
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Name | BDBM50418061 |
Synonyms: | CHEMBL1688971 |
Type | Small organic molecule |
Emp. Form. | C14H21N5 |
Mol. Mass. | 259.35 |
SMILES | C(Cc1cnc[nH]1)Cn1cc(nn1)C1CCCCC1 |
Structure |
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