Reaction Details |
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Target | 5-hydroxytryptamine receptor 1A |
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Ligand | BDBM50316682 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_632233 (CHEMBL1110095) |
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Ki | 0.61±n/a nM |
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Citation | Childers, WE; Havran, LM; Asselin, M; Bicksler, JJ; Chong, DC; Grosu, GT; Shen, Z; Abou-Gharbia, MA; Bach, AC; Harrison, BL; Kagan, N; Kleintop, T; Magolda, R; Marathias, V; Robichaud, AJ; Sabb, AL; Zhang, MY; Andree, TH; Aschmies, SH; Beyer, C; Comery, TA; Day, M; Grauer, SM; Hughes, ZA; Rosenzweig-Lipson, S; Platt, B; Pulicicchio, C; Smith, DE; Sukoff-Rizzo, SJ; Sullivan, KM; Adedoyin, A; Huselton, C; Hirst, WD The synthesis and biological evaluation of quinolyl-piperazinyl piperidines as potent serotonin 5-HT1A antagonists. J Med Chem53:4066-84 (2010) [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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BDBM50316682 |
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n/a |
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Name | BDBM50316682 |
Synonyms: | 6-Bromo-8-{4-[4-(6-methoxyquinolin-8-yl)piperazin-1-yl]piperidin-1-yl}Quinoline | CHEMBL1096529 |
Type | Small organic molecule |
Emp. Form. | C28H30BrN5O |
Mol. Mass. | 532.475 |
SMILES | COc1cc(N2CCN(CC2)C2CCN(CC2)c2cc(Br)cc3cccnc23)c2ncccc2c1 |
Structure |
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