Reaction Details |
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Target | 5-hydroxytryptamine receptor 2A |
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Ligand | BDBM152816 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Receptor Binding Assay |
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pH | 7.5±n/a |
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IC50 | 15.1±n/a nM |
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Comments | extracted |
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Citation | Zhang, G; Chen, Y; Xu, X; Liu, B; Feng, X; Zhao, S; Liu, S; Yu, M; Lan, Y; Qiu, Y [1,3,4] oxadiazole derivative and application thereof US Patent US8993575 Publication Date 3/31/2015 |
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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-2A | 5-HT2 | 5-HT2A | 5-hydroxytryptamine receptor 2A (5-HT2A) | 5-hydroxytryptamine receptor 2A (5HT2A) | 5HT2A_RAT | Htr2 | Htr2a | Serotonin Receptor 2A |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 52852.05 |
Organism: | Rattus norvegicus (rat) |
Description: | Rat cortex membranes 5-HT2A receptors. |
Residue: | 471 |
Sequence: | MEILCEDNISLSSIPNSLMQLGDGPRLYHNDFNSRDANTSEASNWTIDAENRTNLSCEGY
LPPTCLSILHLQEKNWSALLTTVVIILTIAGNILVIMAVSLEKKLQNATNYFLMSLAIAD
MLLGFLVMPVSMLTILYGYRWPLPSKLCAIWIYLDVLFSTASIMHLCAISLDRYVAIQNP
IHHSRFNSRTKAFLKIIAVWTISVGISMPIPVFGLQDDSKVFKEGSCLLADDNFVLIGSF
VAFFIPLTIMVITYFLTIKSLQKEATLCVSDLSTRAKLASFSFLPQSSLSSEKLFQRSIH
REPGSYAGRRTMQSISNEQKACKVLGIVFFLFVVMWCPFFITNIMAVICKESCNENVIGA
LLNVFVWIGYLSSAVNPLVYTLFNKTYRSAFSRYIQCQYKENRKPLQLILVNTIPALAYK
SSQLQVGQKKNSQEDAEQTVDDCSMVTLGKQQSEENCTDNIETVNEKVSCV
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BDBM152816 |
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n/a |
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Name | BDBM152816 |
Synonyms: | US8993575, 6 |
Type | Small organic molecule |
Emp. Form. | C23H22ClFN4O2S |
Mol. Mass. | 472.963 |
SMILES | Fc1ccc2c(noc2c1)C1CCN(CCCSc2nnc(o2)-c2ccc(Cl)cc2)CC1 |
Structure |
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