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SMILES: CN1CCc2c(C1)cnc1c(c(C)nn21)S(=O)(=O)c1ccccc1

InChI Key: InChIKey=HXWBAPBYAWNJPM-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 = 50396233   
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 6


(Homo sapiens (Human))
BDBM50396233
PNG
(CHEMBL2172182 | US8569318, 1.1(3))
Show SMILES CN1CCc2c(C1)cnc1c(c(C)nn21)S(=O)(=O)c1ccccc1
Show InChI InChI=1S/C17H18N4O2S/c1-12-16(24(22,23)14-6-4-3-5-7-14)17-18-10-13-11-20(2)9-8-15(13)21(17)19-12/h3-7,10H,8-9,11H2,1-2H3
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PC sid
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Similars

US Patent
60n/a 13n/an/an/an/an/an/a



TBA

US Patent


Assay Description
Activity test of serotonin 5-HT6 receptor antagonists of the general formulas 1, 2 in the setting of competitive binding to serotonin 5-HT6 receptors...


US Patent US8569318 (2013)


BindingDB Entry DOI: 10.7270/Q2JH3JT8
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 6


(Homo sapiens (Human))
BDBM50396233
PNG
(CHEMBL2172182 | US8569318, 1.1(3))
Show SMILES CN1CCc2c(C1)cnc1c(c(C)nn21)S(=O)(=O)c1ccccc1
Show InChI InChI=1S/C17H18N4O2S/c1-12-16(24(22,23)14-6-4-3-5-7-14)17-18-10-13-11-20(2)9-8-15(13)21(17)19-12/h3-7,10H,8-9,11H2,1-2H3
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
60.4n/an/an/an/an/an/an/an/a



Chemical Diversity Research Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]lysergic acid diethylamide from human recombinant 5HT6 receptor expressed in HeLa cells after 120 mins


Bioorg Med Chem Lett 22: 4273-80 (2012)


Article DOI: 10.1016/j.bmcl.2012.05.036
BindingDB Entry DOI: 10.7270/Q2VH5PZ8
More data for this
Ligand-Target Pair