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SMILES: O=S(=O)(c1nccc2sncc12)n1cc(C2=CCNCC2)c2ccccc12

InChI Key: InChIKey=GRDKGQSOKNBODD-UHFFFAOYSA-N

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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50158036   
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))
BDBM50158036
PNG
(4-[3-(1,2,3,6-Tetrahydro-pyridin-4-yl)-indole-1-su...)
Show SMILES O=S(=O)(c1nccc2sncc12)n1cc(C2=CCNCC2)c2ccccc12 |t:17|
Show InChI InChI=1S/C19H16N4O2S2/c24-27(25,19-15-11-22-26-18(15)7-10-21-19)23-12-16(13-5-8-20-9-6-13)14-3-1-2-4-17(14)23/h1-5,7,10-12,20H,6,8-9H2
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KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
5n/an/an/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Binding affinity against cloned human 5-hydroxytryptamine 6 receptor expressed in HeLa cells using [3H]-LSD


Bioorg Med Chem Lett 15: 379-83 (2004)


Article DOI: 10.1016/j.bmcl.2004.10.064
BindingDB Entry DOI: 10.7270/Q20G3JNQ
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 6


(Homo sapiens (Human))
BDBM50158036
PNG
(4-[3-(1,2,3,6-Tetrahydro-pyridin-4-yl)-indole-1-su...)
Show SMILES O=S(=O)(c1nccc2sncc12)n1cc(C2=CCNCC2)c2ccccc12 |t:17|
Show InChI InChI=1S/C19H16N4O2S2/c24-27(25,19-15-11-22-26-18(15)7-10-21-19)23-12-16(13-5-8-20-9-6-13)14-3-1-2-4-17(14)23/h1-5,7,10-12,20H,6,8-9H2
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 169n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
Inhibitory concentration against 5-HT stimulated cAMP production in HeLa cells stably transfected with human 5-HT6 receptor


Bioorg Med Chem Lett 15: 379-83 (2004)


Article DOI: 10.1016/j.bmcl.2004.10.064
BindingDB Entry DOI: 10.7270/Q20G3JNQ
More data for this
Ligand-Target Pair