Reaction Details |
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Target | Histamine H4 receptor |
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Ligand | BDBM189353 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1799139 (CHEMBL4271431) |
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Ki | 7500±n/a nM |
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Citation | Cascioferro, S; Parrino, B; Spanò, V; Carbone, A; Montalbano, A; Barraja, P; Diana, P; Cirrincione, G 1,3,5-Triazines: A promising scaffold for anticancer drugs development. Eur J Med Chem142:523-549 (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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BDBM189353 |
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n/a |
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Name | BDBM189353 |
Synonyms: | 4-Benzyl-6-(4-methylpiperazin-1-yl)-1,3,5-triazin-2-amine (13) |
Type | Small organic molecule |
Emp. Form. | C15H20N6 |
Mol. Mass. | 284.3595 |
SMILES | CN1CCN(CC1)c1nc(N)nc(Cc2ccccc2)n1 |
Structure |
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