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| Reaction Details | |||
|---|---|---|---|
 | Report a problem with these data | ||
| Target | 5-hydroxytryptamine receptor 2A | ||
| Ligand | BDBM106466 | ||
| Substrate/Competitor | n/a | ||
| Meas. Tech. | Radioligand Binding Assay | ||
| Ki | 6.14±0.0 nM | ||
| Citation |  Gobbi, L; Rodriguez Sarmiento, RM; Wichmann, J Anellated pyridine compounds US Patent US8586579 Publication Date 11/19/2013 | ||
| More Info.: | Get all data from this article, Assay Method | ||
| 5-hydroxytryptamine receptor 2A | |||
| Name: | 5-hydroxytryptamine receptor 2A | ||
| Synonyms: | 5-HT-2 | 5-HT-2A | 5-HT2A | 5-hydroxytryptamine receptor 2A (5-HT-2A) | 5-hydroxytryptamine receptor 2A (5HT-2A) | 5-hydroxytryptamine receptor 2A (5HT2A) | 5HT2A_HUMAN | HTR2 | HTR2A | Serotonin receptor 2A | ||
| Type: | undefined | ||
| Mol. Mass.: | 52607.65 | ||
| Organism: | Homo sapiens (Human) | ||
| Description: | P28223 | ||
| Residue: | 471 | ||
| Sequence: |
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| BDBM106466 | |||
| n/a | |||
| Name | BDBM106466 | ||
| Synonyms: | US8586579, 55 | ||
| Type | Small organic molecule | ||
| Emp. Form. | C27H42N4O3 | ||
| Mol. Mass. | 470.6474 | ||
| SMILES | C[C@@]1(O)CC[C@@H](CC1)C(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2nccc3OCCc23)CC1 |r,wU:11.11,1.0,wD:14.15,5.8,1.1,(11.45,1.29,;10.11,.52,;11.45,-.25,;9.34,-.82,;7.8,-.82,;7.03,.52,;7.8,1.85,;9.34,1.85,;5.49,.52,;4.72,-.82,;4.72,1.85,;3.18,1.85,;2.41,.52,;.87,.52,;.1,1.85,;-1.44,1.85,;-2.21,.52,;-3.75,.52,;-4.52,-.82,;-6.06,-.82,;-6.83,.52,;-6.06,1.85,;-4.52,1.85,;-8.37,.52,;-9.14,1.85,;-10.68,1.85,;-11.45,.52,;-10.68,-.82,;-11.15,-2.28,;-9.91,-3.19,;-8.66,-2.28,;-9.14,-.82,;.87,3.19,;2.41,3.19,)| | ||
| Structure | 
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