Reaction Details |
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Target | Histamine H4 receptor |
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Ligand | BDBM50325746 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1691274 (CHEMBL4041923) |
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Ki | 51±n/a nM |
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Citation | Levoin, N; Labeeuw, O; Billot, X; Calmels, T; Danvy, D; Krief, S; Berrebi-Bertrand, I; Lecomte, JM; Schwartz, JC; Capet, M Discovery of nanomolar ligands with novel scaffolds for the histamine H4 receptor by virtual screening. Eur J Med Chem125:565-572 (2017) [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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BDBM50325746 |
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n/a |
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Name | BDBM50325746 |
Synonyms: | CHEMBL1223748 | N-(4-(4-(2-methoxyphenyl)piperazin-1-yl)butyl)isoquinolin-1-amine |
Type | Small organic molecule |
Emp. Form. | C24H30N4O |
Mol. Mass. | 390.5212 |
SMILES | COc1ccccc1N1CCN(CCCCNc2nccc3ccccc23)CC1 |
Structure |
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