Reaction Details |
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Target | 5-hydroxytryptamine receptor 1A |
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Ligand | BDBM50191632 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_376264 (CHEMBL864775) |
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Ki | 2.3±n/a nM |
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Citation | Hatzenbuhler, NT; Evrard, DA; Harrison, BL; Huryn, D; Inghrim, J; Kraml, C; Mattes, JF; Mewshaw, RE; Zhou, D; Hornby, G; Lin, Q; Smith, DL; Sullivan, KM; Schechter, LE; Beyer, CE; Andree, TH Synthesis and biological evaluation of novel compounds within a class of 3-aminochroman derivatives with dual 5-HT1A receptor and serotonin transporter affinity. J Med Chem49:4785-9 (2006) [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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BDBM50191632 |
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n/a |
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Name | BDBM50191632 |
Synonyms: | CHEMBL209262 | rac-N-ethyl-N-[3-(5-fluoro-1H-indol-3-yl)propyl]-5-methoxychroman-3-amine |
Type | Small organic molecule |
Emp. Form. | C23H27FN2O2 |
Mol. Mass. | 382.4711 |
SMILES | CCN(CCCc1c[nH]c2ccc(F)cc12)C1COc2cccc(OC)c2C1 |
Structure |
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