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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | 5-hydroxytryptamine receptor 1A | ||
| Ligand | BDBM50207090 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | ChEBML_1630051 | ||
| Ki | 1.1±n/a nM | ||
| Citation |  Chen, XW; Sun, YY; Fu, L; Li, JQ Synthesis and pharmacological characterization of novel N-(trans-4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl)cyclohexyl)amides as potential multireceptor atypical antipsychotics. Eur J Med Chem123:332-353 (2016) [PubMed] Article | ||
| More Info.: | Get all data from this article, Assay Method | ||
| 5-hydroxytryptamine receptor 1A | |||
| 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: |
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| BDBM50207090 | |||
| n/a | |||
| Name | BDBM50207090 | ||
| Synonyms: | CHEMBL3913691 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C21H27F3N4OS | ||
| Mol. Mass. | 440.525 | ||
| SMILES | FC(F)(F)C(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2nsc3ccccc23)CC1 |r,wU:7.6,wD:10.10,(11.43,-20.1,;11.8,-21.5,;10.77,-22.53,;10.39,-21.12,;13.28,-21.91,;13.7,-23.4,;14.31,-20.73,;15.81,-21.09,;16.83,-19.91,;18.37,-20.21,;18.83,-21.71,;20.33,-22.01,;21.35,-20.89,;22.89,-21.2,;23.35,-22.68,;24.85,-23,;25.87,-21.86,;25.41,-20.37,;23.92,-20.06,;27.41,-22.17,;28.03,-23.56,;29.57,-23.4,;29.88,-21.91,;31.22,-21.15,;31.22,-19.6,;29.88,-18.83,;28.55,-19.6,;28.55,-21.15,;17.81,-22.84,;16.32,-22.52,)| | ||
| Structure | 
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