Reaction Details |
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Target | 5-hydroxytryptamine receptor 1A |
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Ligand | BDBM50286084 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_1446 |
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Ki | 47±n/a nM |
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Citation | Dahlgren, T; Dean, RL; Gharat, LA; Johansson, AM; Lambert, G; Li, HB; Nelson, DL; Yang, Y; Martin, AR Synthesis and serotonin receptor binding properties of 5-substituted 3-(1′,2′,5′,6′-tetrahydropyridin-3′-yl) indoles Bioorg Med Chem Lett5:2963-2968 (1995) 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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BDBM50286084 |
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n/a |
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Name | BDBM50286084 |
Synonyms: | 5-Chloro-3-(1-ethyl-1,2,5,6-tetrahydro-pyridin-3-yl)-1H-indole | CHEMBL101258 |
Type | Small organic molecule |
Emp. Form. | C15H17ClN2 |
Mol. Mass. | 260.762 |
SMILES | CCN1CCC=C(C1)c1c[nH]c2ccc(Cl)cc12 |c:5| |
Structure |
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