Reaction Details |
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Target | 5-hydroxytryptamine receptor 1F |
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Ligand | BDBM50130461 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1518515 (CHEMBL3618901) |
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Ki | 2.1±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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BDBM50130461 |
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n/a |
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Name | BDBM50130461 |
Synonyms: | 4-Fluoro-N-[3-(1-methyl-4-piperidinyl)-1H-indol-5-yl]benzamide | 4-Fluoro-N-[3-(1-methyl-piperidin-4-yl)-1H-indol-5-yl]-benzamide | CHEMBL101690 | LY-334370 |
Type | Small organic molecule |
Emp. Form. | C21H22FN3O |
Mol. Mass. | 351.4173 |
SMILES | CN1CCC(CC1)c1c[nH]c2ccc(NC(=O)c3ccc(F)cc3)cc12 |
Structure |
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