Reaction Details |
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Target | 5-hydroxytryptamine receptor 1A |
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Ligand | BDBM50059468 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1472 (CHEMBL616595) |
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Ki | 13.9±n/a nM |
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Citation | López-Rodríguez, ML; Morcillo, MJ; Fernández, E; Porras, E; Murcia, M; Sanz, AM; Orensanz, L Synthesis and structure-activity relationships of a new model of arylpiperazines. 3.1 2-[omega-(4-arylpiperazin-1-yl)alkyl]perhydropyrrolo- [1,2-c]imidazoles and -perhydroimidazo[1,5-a]pyridines: study of the influence of the terminal amide fragment on 5-HT1A affinity/selectivity. J Med Chem40:2653-6 (1997) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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5-hydroxytryptamine receptor 1A |
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Name: | 5-hydroxytryptamine receptor 1A |
Synonyms: | 5-HT-1A | 5-HT1 | 5-HT1A | 5-Hydroxytryptamine receptor 1A (5-HT1A) | 5-hydroxytryptamine receptor 1A (5HT1A) | 5HT1A_RAT | 5ht1a | G-21 | Htr1a | Serotonin 1 (5-HT1) receptor | Serotonin 1a (5-HT1a) receptor/Adrenergic receptor alpha-1 | Serotonin receptor 1A |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 46445.29 |
Organism: | Rattus norvegicus (rat) |
Description: | Binding assays were performed using rat hippocampal membranes. |
Residue: | 422 |
Sequence: | MDVFSFGQGNNTTASQEPFGTGGNVTSISDVTFSYQVITSLLLGTLIFCAVLGNACVVAA
IALERSLQNVANYLIGSLAVTDLMVSVLVLPMAALYQVLNKWTLGQVTCDLFIALDVLCC
TSSILHLCAIALDRYWAITDPIDYVNKRTPRRAAALISLTWLIGFLISIPPMLGWRTPED
RSDPDACTISKDHGYTIYSTFGAFYIPLLLMLVLYGRIFRAARFRIRKTVRKVEKKGAGT
SLGTSSAPPPKKSLNGQPGSGDWRRCAENRAVGTPCTNGAVRQGDDEATLEVIEVHRVGN
SKEHLPLPSESGSNSYAPACLERKNERNAEAKRKMALARERKTVKTLGIIMGTFILCWLP
FFIVALVLPFCESSCHMPALLGAIINWLGYSNSLLNPVIYAYFNKDFQNAFKKIIKCKFC
RR
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BDBM50059468 |
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n/a |
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Name | BDBM50059468 |
Synonyms: | 2-{3-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-propyl}-octahydro-imidazo[1,5-a]pyridine | CHEMBL89380 |
Type | Small organic molecule |
Emp. Form. | C21H34N4O |
Mol. Mass. | 358.5209 |
SMILES | COc1ccccc1N1CCN(CCCN2CC3CCCCN3C2)CC1 |
Structure |
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