BDBM50070407 2N,2N-dipropyl-8-[6-(3-dipropylamino-1,2,3,4-tetrahydro-5-naphthalenyloxy)hexyloxy]-1,2,3,4-tetrahydro-2-naphthalenamine::CHEMBL29951

SMILES CCCN(CCC)C1CCc2cccc(OCCCCCCOc3cccc4CCC(Cc34)N(CCC)CCC)c2C1

InChI Key InChIKey=HLPZOVNKHVYFCY-UHFFFAOYSA-N

Data  3 KI  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50070407   

Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
Centre De Recherche Pierre Fabre

Curated by ChEMBL
LigandPNGBDBM50070407(2N,2N-dipropyl-8-[6-(3-dipropylamino-1,2,3,4-tetra...)
Affinity DataKi:  3.90nMAssay Description:Binding affinity of the compound was evaluated at human recombinant 5-hydroxytryptamine 1D receptor using [3H]-5-CT as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
Centre De Recherche Pierre Fabre

Curated by ChEMBL
LigandPNGBDBM50070407(2N,2N-dipropyl-8-[6-(3-dipropylamino-1,2,3,4-tetra...)
Affinity DataKi:  6.40nMAssay Description:The intrinsic activity of the compound was evaluated for its ability to inhibit forskolin-stimulated c-AMP formation mediated by cloned 5-hydroxytryp...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Centre De Recherche Pierre Fabre

Curated by ChEMBL
LigandPNGBDBM50070407(2N,2N-dipropyl-8-[6-(3-dipropylamino-1,2,3,4-tetra...)
Affinity DataKi:  6.80nMAssay Description:Binding affinity of the compound was evaluated at human recombinant 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Homo sapiens (Human))
Centre De Recherche Pierre Fabre

Curated by ChEMBL
LigandPNGBDBM50070407(2N,2N-dipropyl-8-[6-(3-dipropylamino-1,2,3,4-tetra...)
Affinity DataEC50:  50nMAssay Description:The intrinsic activity of the compound was evaluated for its ability to inhibit forskolin-stimulated c-AMP formation mediated by cloned 5-hydroxytryp...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed