Reaction Details |
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Target | 5-hydroxytryptamine receptor 2A |
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Ligand | BDBM50145587 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1556023 (CHEMBL3767882) |
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Ki | 0.793000±n/a nM |
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Citation | Fiorino, F; Ciano, A; Magli, E; Severino, B; Corvino, A; Perissutti, E; Frecentese, F; Di Vaio, P; Izzo, AA; Capasso, R; Massarelli, P; Nencini, C; Rossi, I; Kedzierska, E; Orzelska-Gòrka, J; Bielenica, A; Santagada, V; Caliendo, G Synthesis, in vitro and in vivo pharmacological evaluation of serotoninergic ligands containing an isonicotinic nucleus. Eur J Med Chem110:133-50 (2016) [PubMed] Article |
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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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BDBM50145587 |
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n/a |
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Name | BDBM50145587 |
Synonyms: | CHEMBL3764080 |
Type | Small organic molecule |
Emp. Form. | C20H24N4O3 |
Mol. Mass. | 368.4296 |
SMILES | O=C(NCCN1CCN(Cc2ccc3OCOc3c2)CC1)c1ccncc1 |
Structure |
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