Reaction Details |
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Target | 5-hydroxytryptamine receptor 2A |
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Ligand | BDBM50596723 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2222119 (CHEMBL5135453) |
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IC50 | 0.540000±n/a nM |
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Citation | Ma, M; Yang, Y; Du, G; Dai, Y; Zhu, X; Wang, W; Xu, H; Zhang, J; Zheng, L; Zou, F; Yang, H; Liu, B; Liu, W; Ye, L; Zhang, R; Tian, J Improving the treatment of Parkinson's disease: Structure-based development of novel 5-HT Eur J Med Chem234:0 (2022) [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-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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BDBM50596723 |
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n/a |
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Name | BDBM50596723 |
Synonyms: | CHEMBL5205903 | US20230348421, Compound 59 |
Type | Small organic molecule |
Emp. Form. | C22H26F4N4O2 |
Mol. Mass. | 454.4611 |
SMILES | CN1CCC(CC1)N(Cc1ccc(F)cn1)C(=O)NCc1ccc(OCC(F)(F)F)cc1 |
Structure |
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