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Target5-hydroxytryptamine receptor 1F
LigandBDBM50130461
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1518515 (CHEMBL3618901)
Ki 2.1±n/a nM
Citation Zhang, DBlanco, MJYing, BPKohlman, DLiang, SXVictor, FChen, QKrushinski, JFilla, SAHudziak, KJMathes, BMCohen, MPZacherl, DNelson, DLWainscott, DBNutter, SEGough, WHSchaus, JMXu, 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
More Info.:Get all data from this article,  Assay Method
 
5-hydroxytryptamine receptor 1F
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50130461
n/a
NameBDBM50130461
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
TypeSmall organic molecule
Emp. Form.C21H22FN3O
Mol. Mass.351.4173
SMILESCN1CCC(CC1)c1c[nH]c2ccc(NC(=O)c3ccc(F)cc3)cc12
Structure
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