Reaction Details |
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Target | 5-hydroxytryptamine receptor 1A |
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Ligand | BDBM50029270 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1143 (CHEMBL616088) |
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Ki | 1.9±n/a nM |
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Citation | Scott, MK; Baxter, EW; Bennett, DJ; Boyd, RE; Blum, PS; Codd, EE; Kukla, MJ; Malloy, E; Maryanoff, BE; Maryanoff, CA Piperazinylalkyl heterocycles as potential antipsychotic agents. J Med Chem38:4198-210 (1995) [PubMed] |
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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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BDBM50029270 |
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n/a |
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Name | BDBM50029270 |
Synonyms: | 2-{5-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-furan-2-ylmethyl}-isoindole-1,3-dione | CHEMBL133765 |
Type | Small organic molecule |
Emp. Form. | C25H25N3O4 |
Mol. Mass. | 431.4837 |
SMILES | COc1ccccc1N1CCN(Cc2ccc(CN3C(=O)c4ccccc4C3=O)o2)CC1 |
Structure |
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