Reaction Details |
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Target | 5-hydroxytryptamine receptor 1A |
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Ligand | BDBM50206761 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1629238 (CHEMBL3871864) |
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Ki | 0.360000±n/a nM |
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Citation | Yoshinaga, H; Masumoto, S; Koyama, K; Kinomura, N; Matsumoto, Y; Kato, T; Baba, S; Matsumoto, K; Horisawa, T; Oki, H; Yabuuchi, K; Kodo, T Discovery of SMP-304, a novel benzylpiperidine derivative with serotonin transporter inhibitory activity and 5-HT Bioorg Med Chem25:293-304 (2017) [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-HT1A | 5-hydroxytryptamine receptor 1A (5-HT-1A) | 5HT1A_HUMAN | ADRB2RL1 | ADRBRL1 | Dopamine D2 receptor and serotonin 1a receptor | G-21 | HTR1A | Serotonin receptor 1A |
Type: | n/a |
Mol. Mass.: | 46122.49 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 422 |
Sequence: | MDVLSPGQGNNTTSPPAPFETGGNTTGISDVTVSYQVITSLLLGTLIFCAVLGNACVVAA
IALERSLQNVANYLIGSLAVTDLMVSVLVLPMAALYQVLNKWTLGQVTCDLFIALDVLCC
TSSILHLCAIALDRYWAITDPIDYVNKRTPRRAAALISLTWLIGFLISIPPMLGWRTPED
RSDPDACTISKDHGYTIYSTFGAFYIPLLLMLVLYGRIFRAARFRIRKTVKKVEKTGADT
RHGASPAPQPKKSVNGESGSRNWRLGVESKAGGALCANGAVRQGDDGAALEVIEVHRVGN
SKEHLPLPSEAGPTPCAPASFERKNERNAEAKRKMALARERKTVKTLGIIMGTFILCWLP
FFIVALVLPFCESSCHMPTLLGAIINWLGYSNSLLNPVIYAYFNKDFQNAFKKIIKCKFC
RQ
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BDBM50206761 |
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n/a |
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Name | BDBM50206761 |
Synonyms: | CHEMBL3958278 |
Type | Small organic molecule |
Emp. Form. | C23H28BrNO3 |
Mol. Mass. | 446.377 |
SMILES | COc1ccc(Br)c(CC2CCN(CCc3ccc4OCCOc4c3)CC2)c1 |
Structure |
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