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SMILES: CN1CCC(CC1)c1noc2ccc(NC(=O)c3ccc(F)cc3F)cc12

InChI Key: InChIKey=XMLPQEYFKNHQHR-UHFFFAOYSA-N

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50156406   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
5-hydroxytryptamine receptor 1F


(Homo sapiens (Human))
BDBM50156406
PNG
(2,4-Difluoro-N-[3-(1-methyl-piperidin-4-yl)-benzo[...)
Show SMILES CN1CCC(CC1)c1noc2ccc(NC(=O)c3ccc(F)cc3F)cc12
Show InChI InChI=1S/C20H19F2N3O2/c1-25-8-6-12(7-9-25)19-16-11-14(3-5-18(16)27-24-19)23-20(26)15-4-2-13(21)10-17(15)22/h2-5,10-12H,6-9H2,1H3,(H,23,26)
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PC cid
PC sid
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Similars

Article
PubMed
12n/an/an/an/an/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
In vitro binding affinity for human 5-hydroxytryptamine 1F receptor


Bioorg Med Chem Lett 14: 6011-6 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.079
BindingDB Entry DOI: 10.7270/Q23J3CFK
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1F


(Homo sapiens (Human))
BDBM50156406
PNG
(2,4-Difluoro-N-[3-(1-methyl-piperidin-4-yl)-benzo[...)
Show SMILES CN1CCC(CC1)c1noc2ccc(NC(=O)c3ccc(F)cc3F)cc12
Show InChI InChI=1S/C20H19F2N3O2/c1-25-8-6-12(7-9-25)19-16-11-14(3-5-18(16)27-24-19)23-20(26)15-4-2-13(21)10-17(15)22/h2-5,10-12H,6-9H2,1H3,(H,23,26)
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 470n/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
Stimulation of [35S]-GTP-gammaS, binding to cloned human 5-hydroxytryptamine 1F receptor expressed in Mouse LM(tk-) cells


Bioorg Med Chem Lett 14: 6011-6 (2004)


Article DOI: 10.1016/j.bmcl.2004.09.079
BindingDB Entry DOI: 10.7270/Q23J3CFK
More data for this
Ligand-Target Pair