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BDBM50413564 CHEMBL469589

SMILES: CN1C(=O)COc2c(CCCN3CCN(CC3)c3cc(F)cc4nc(C)ccc34)cccc12

InChI Key: InChIKey=DFRRWIGBGSRDTE-UHFFFAOYSA-N

Data: 5 KI

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50413564   
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
Sodium-dependent serotonin transporter


(Homo sapiens (Human))
BDBM50413564
PNG
(CHEMBL469589)
Show SMILES CN1C(=O)COc2c(CCCN3CCN(CC3)c3cc(F)cc4nc(C)ccc34)cccc12
Show InChI InChI=1S/C26H29FN4O2/c1-18-8-9-21-22(28-18)15-20(27)16-24(21)31-13-11-30(12-14-31)10-4-6-19-5-3-7-23-26(19)33-17-25(32)29(23)2/h3,5,7-9,15-16H,4,6,10-14,17H2,1-2H3
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PubMed
0.316n/an/an/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Displacement of [3H]citalopram human SerT receptor expressed in LLCPK cells


Bioorg Med Chem Lett 19: 2338-42 (2009)


Article DOI: 10.1016/j.bmcl.2009.02.056
BindingDB Entry DOI: 10.7270/Q2J967MX
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1A


(Homo sapiens (Human))
BDBM50413564
PNG
(CHEMBL469589)
Show SMILES CN1C(=O)COc2c(CCCN3CCN(CC3)c3cc(F)cc4nc(C)ccc34)cccc12
Show InChI InChI=1S/C26H29FN4O2/c1-18-8-9-21-22(28-18)15-20(27)16-24(21)31-13-11-30(12-14-31)10-4-6-19-5-3-7-23-26(19)33-17-25(32)29(23)2/h3,5,7-9,15-16H,4,6,10-14,17H2,1-2H3
PDB

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PubMed
6.31n/an/an/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Antagonist activity at human 5HT1A assessed as GTPgammaS binding by scintillation proximity assay in presence of 5-HT


Bioorg Med Chem Lett 19: 2338-42 (2009)


Article DOI: 10.1016/j.bmcl.2009.02.056
BindingDB Entry DOI: 10.7270/Q2J967MX
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1D


(Homo sapiens (Human))
BDBM50413564
PNG
(CHEMBL469589)
Show SMILES CN1C(=O)COc2c(CCCN3CCN(CC3)c3cc(F)cc4nc(C)ccc34)cccc12
Show InChI InChI=1S/C26H29FN4O2/c1-18-8-9-21-22(28-18)15-20(27)16-24(21)31-13-11-30(12-14-31)10-4-6-19-5-3-7-23-26(19)33-17-25(32)29(23)2/h3,5,7-9,15-16H,4,6,10-14,17H2,1-2H3
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15.8n/an/an/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Antagonist activity at human 5HT1D assessed as GTPgammaS binding by scintillation proximity assay in presence of 5-HT


Bioorg Med Chem Lett 19: 2338-42 (2009)


Article DOI: 10.1016/j.bmcl.2009.02.056
BindingDB Entry DOI: 10.7270/Q2J967MX
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 1B


(Homo sapiens (Human))
BDBM50413564
PNG
(CHEMBL469589)
Show SMILES CN1C(=O)COc2c(CCCN3CCN(CC3)c3cc(F)cc4nc(C)ccc34)cccc12
Show InChI InChI=1S/C26H29FN4O2/c1-18-8-9-21-22(28-18)15-20(27)16-24(21)31-13-11-30(12-14-31)10-4-6-19-5-3-7-23-26(19)33-17-25(32)29(23)2/h3,5,7-9,15-16H,4,6,10-14,17H2,1-2H3
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794n/an/an/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Antagonist activity at human 5HT1B assessed as GTPgammaS binding by scintillation proximity assay in presence of 5-HT


Bioorg Med Chem Lett 19: 2338-42 (2009)


Article DOI: 10.1016/j.bmcl.2009.02.056
BindingDB Entry DOI: 10.7270/Q2J967MX
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50413564
PNG
(CHEMBL469589)
Show SMILES CN1C(=O)COc2c(CCCN3CCN(CC3)c3cc(F)cc4nc(C)ccc34)cccc12
Show InChI InChI=1S/C26H29FN4O2/c1-18-8-9-21-22(28-18)15-20(27)16-24(21)31-13-11-30(12-14-31)10-4-6-19-5-3-7-23-26(19)33-17-25(32)29(23)2/h3,5,7-9,15-16H,4,6,10-14,17H2,1-2H3
PDB
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Article
PubMed
6.31E+3n/an/an/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Displacement of [3H]dofetilide human ERG expressed in CHO cells


Bioorg Med Chem Lett 19: 2338-42 (2009)


Article DOI: 10.1016/j.bmcl.2009.02.056
BindingDB Entry DOI: 10.7270/Q2J967MX
More data for this
Ligand-Target Pair