Reaction Details |
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Target | 5-hydroxytryptamine receptor 1F |
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Ligand | BDBM50119539 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1518515 (CHEMBL3618901) |
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Ki | 530±n/a nM |
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Citation | Zhang, D; Blanco, MJ; Ying, BP; Kohlman, D; Liang, SX; Victor, F; Chen, Q; Krushinski, J; Filla, SA; Hudziak, KJ; Mathes, BM; Cohen, MP; Zacherl, D; Nelson, DL; Wainscott, DB; Nutter, SE; Gough, WH; Schaus, JM; Xu, YC Discovery of selective N-[3-(1-methyl-piperidine-4-carbonyl)-phenyl]-benzamide-based 5-HT1 F receptor agonists: Evolution from bicyclic to monocyclic cores. Bioorg Med Chem Lett25:4337-41 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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5-hydroxytryptamine receptor 1F |
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Name: | 5-hydroxytryptamine receptor 1F |
Synonyms: | 5-HT-1F | 5-HT1F | 5-hydroxytryptamine receptor 1F | 5HT1F_HUMAN | HTR1EL | HTR1F | Serotonin (5-HT) receptor | Serotonin 1f (5-HT1f) receptor | Serotonin receptor 1F |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 41724.68 |
Organism: | Homo sapiens (Human) |
Description: | 5-HT1F HTR1F HUMAN::P30939 |
Residue: | 366 |
Sequence: | MDFLNSSDQNLTSEELLNRMPSKILVSLTLSGLALMTTTINSLVIAAIIVTRKLHHPANY
LICSLAVTDFLVAVLVMPFSIVYIVRESWIMGQVVCDIWLSVDITCCTCSILHLSAIALD
RYRAITDAVEYARKRTPKHAGIMITIVWIISVFISMPPLFWRHQGTSRDDECIIKHDHIV
STIYSTFGAFYIPLALILILYYKIYRAAKTLYHKRQASRIAKEEVNGQVLLESGEKSTKS
VSTSYVLEKSLSDPSTDFDKIHSTVRSLRSEFKHEKSWRRQKISGTRERKAATTLGLILG
AFVICWLPFFVKELVVNVCDKCKISEEMSNFLAWLGYLNSLINPLIYTIFNEDFKKAFQK
LVRCRC
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BDBM50119539 |
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n/a |
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Name | BDBM50119539 |
Synonyms: | CHEMBL3617553 |
Type | Small organic molecule |
Emp. Form. | C20H20F2N2O2 |
Mol. Mass. | 358.3818 |
SMILES | CN1CCC(CC1)C(=O)c1ccc(F)c(NC(=O)c2ccc(F)cc2)c1 |
Structure |
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