Reaction Details |
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Target | 5-hydroxytryptamine receptor 2A |
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Ligand | BDBM570543 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Receptor Selection and Amplification (R-SAT) Assays |
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Ki | 0.251±n/a nM |
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Citation | Burstein, ES; Olsson, R; Jansson, KE; Sköld, NP; Wahlström, LY; Borgström, BG; Von Wachenfeldt, H; Bergner, MG Compounds, salts thereof and methods for treatment of diseases US Patent US11440884 Publication Date 9/13/2022 |
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More Info.: | Get all data from this article, Assay Method |
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5-hydroxytryptamine receptor 2A |
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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: | MDILCEENTSLSSTTNSLMQLNDDTRLYSNDFNSGEANTSDAFNWTVDSENRTNLSCEGC
LSPSCLSLLHLQEKNWSALLTAVVIILTIAGNILVIMAVSLEKKLQNATNYFLMSLAIAD
MLLGFLVMPVSMLTILYGYRWPLPSKLCAVWIYLDVLFSTASIMHLCAISLDRYVAIQNP
IHHSRFNSRTKAFLKIIAVWTISVGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSF
VSFFIPLTIMVITYFLTIKSLQKEATLCVSDLGTRAKLASFSFLPQSSLSSEKLFQRSIH
REPGSYTGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVICKESCNEDVIGA
LLNVFVWIGYLSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENKKPLQLILVNTIPALAYK
SSQLQMGQKKNSKQDAKTTDNDCSMVALGKQHSEEASKDNSDGVNEKVSCV
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BDBM570543 |
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n/a |
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Name | BDBM570543 |
Synonyms: | US11440884, Example 11 |
Type | Small organic molecule |
Emp. Form. | C23H28F2N2O3 |
Mol. Mass. | 418.4768 |
SMILES | CC(C)Oc1ccc(COC(=O)N(Cc2ccc(F)cc2F)C2CCNCC2)cc1 |
Structure |
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