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PubMed code 18020391

Compile data set for download or QSAR
Found 12 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50227129
PNG
(CHEMBL241329 | N-(1-(4-chloro-3-ethoxybenzyl)piper...)
Show SMILES CCOc1cc(CN2CCC(CC2)NC(=O)c2cncc(C)c2)ccc1Cl
Show InChI InChI=1S/C21H26ClN3O2/c1-3-27-20-11-16(4-5-19(20)22)14-25-8-6-18(7-9-25)24-21(26)17-10-15(2)12-23-13-17/h4-5,10-13,18H,3,6-9,14H2,1-2H3,(H,24,26)
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20n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST5R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50227132
PNG
(4-tert-butyl-N-(1-((1,4-dimethoxynaphthalen-2-yl)m...)
Show SMILES COc1cc(CN2CCC(CC2)NC(=O)c2ccc(cc2)C(C)(C)C)c(OC)c2ccccc12
Show InChI InChI=1S/C29H36N2O3/c1-29(2,3)22-12-10-20(11-13-22)28(32)30-23-14-16-31(17-15-23)19-21-18-26(33-4)24-8-6-7-9-25(24)27(21)34-5/h6-13,18,23H,14-17,19H2,1-5H3,(H,30,32)
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20n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST5R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50227130
PNG
(CHEMBL241328 | N-(1-((1,4-dimethoxynaphthalen-2-yl...)
Show SMILES COc1cc(CN2CCC(CC2)NC(=O)c2cncc(C)c2)c(OC)c2ccccc12
Show InChI InChI=1S/C25H29N3O3/c1-17-12-18(15-26-14-17)25(29)27-20-8-10-28(11-9-20)16-19-13-23(30-2)21-6-4-5-7-22(21)24(19)31-3/h4-7,12-15,20H,8-11,16H2,1-3H3,(H,27,29)
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40n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST5R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50227131
PNG
(CHEMBL241330 | N-(1-(4-chloro-3-ethoxybenzyl)piper...)
Show SMILES CCOc1cc(CN2CCC(CC2)NC(=O)c2cccc(c2)S(C)(=O)=O)ccc1Cl
Show InChI InChI=1S/C22H27ClN2O4S/c1-3-29-21-13-16(7-8-20(21)23)15-25-11-9-18(10-12-25)24-22(26)17-5-4-6-19(14-17)30(2,27)28/h4-8,13-14,18H,3,9-12,15H2,1-2H3,(H,24,26)
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60n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST5R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50227128
PNG
(CHEMBL268075 | N-(1-((1,4-dimethoxynaphthalen-2-yl...)
Show SMILES COc1cc(CN2CCC(CC2)NC(=O)c2ccccc2)c(OC)c2ccccc12
Show InChI InChI=1S/C25H28N2O3/c1-29-23-16-19(24(30-2)22-11-7-6-10-21(22)23)17-27-14-12-20(13-15-27)26-25(28)18-8-4-3-5-9-18/h3-11,16,20H,12-15,17H2,1-2H3,(H,26,28)
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120n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST5R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Histamine H1 receptor


(Homo sapiens (Human))
BDBM50227129
PNG
(CHEMBL241329 | N-(1-(4-chloro-3-ethoxybenzyl)piper...)
Show SMILES CCOc1cc(CN2CCC(CC2)NC(=O)c2cncc(C)c2)ccc1Cl
Show InChI InChI=1S/C21H26ClN3O2/c1-3-27-20-11-16(4-5-19(20)22)14-25-8-6-18(7-9-25)24-21(26)17-10-15(2)12-23-13-17/h4-5,10-13,18H,3,6-9,14H2,1-2H3,(H,24,26)
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270n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human histamine H1 receptor


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50227133
PNG
(1'-[(1,4-dimethoxynaphthalen-2-yl)methyl]-3H-spiro...)
Show SMILES COc1cc(CN2CCC3(CC2)OC(=O)c2ccccc32)c(OC)c2ccccc12
Show InChI InChI=1S/C25H25NO4/c1-28-22-15-17(23(29-2)19-8-4-3-7-18(19)22)16-26-13-11-25(12-14-26)21-10-6-5-9-20(21)24(27)30-25/h3-10,15H,11-14,16H2,1-2H3
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1.10E+3n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST5R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Histamine H1 receptor


(Homo sapiens (Human))
BDBM50227131
PNG
(CHEMBL241330 | N-(1-(4-chloro-3-ethoxybenzyl)piper...)
Show SMILES CCOc1cc(CN2CCC(CC2)NC(=O)c2cccc(c2)S(C)(=O)=O)ccc1Cl
Show InChI InChI=1S/C22H27ClN2O4S/c1-3-29-21-13-16(7-8-20(21)23)15-25-11-9-18(10-12-25)24-22(26)17-5-4-6-19(14-17)30(2,27)28/h4-8,13-14,18H,3,9-12,15H2,1-2H3,(H,24,26)
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>5.00E+3n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human histamine H1 receptor


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50227129
PNG
(CHEMBL241329 | N-(1-(4-chloro-3-ethoxybenzyl)piper...)
Show SMILES CCOc1cc(CN2CCC(CC2)NC(=O)c2cncc(C)c2)ccc1Cl
Show InChI InChI=1S/C21H26ClN3O2/c1-3-27-20-11-16(4-5-19(20)22)14-25-8-6-18(7-9-25)24-21(26)17-10-15(2)12-23-13-17/h4-5,10-13,18H,3,6-9,14H2,1-2H3,(H,24,26)
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5.10E+3n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST1R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50227129
PNG
(CHEMBL241329 | N-(1-(4-chloro-3-ethoxybenzyl)piper...)
Show SMILES CCOc1cc(CN2CCC(CC2)NC(=O)c2cncc(C)c2)ccc1Cl
Show InChI InChI=1S/C21H26ClN3O2/c1-3-27-20-11-16(4-5-19(20)22)14-25-8-6-18(7-9-25)24-21(26)17-10-15(2)12-23-13-17/h4-5,10-13,18H,3,6-9,14H2,1-2H3,(H,24,26)
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>1.00E+4n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST3R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50227129
PNG
(CHEMBL241329 | N-(1-(4-chloro-3-ethoxybenzyl)piper...)
Show SMILES CCOc1cc(CN2CCC(CC2)NC(=O)c2cncc(C)c2)ccc1Cl
Show InChI InChI=1S/C21H26ClN3O2/c1-3-27-20-11-16(4-5-19(20)22)14-25-8-6-18(7-9-25)24-21(26)17-10-15(2)12-23-13-17/h4-5,10-13,18H,3,6-9,14H2,1-2H3,(H,24,26)
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>1.00E+4n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human SST2R


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50227131
PNG
(CHEMBL241330 | N-(1-(4-chloro-3-ethoxybenzyl)piper...)
Show SMILES CCOc1cc(CN2CCC(CC2)NC(=O)c2cccc(c2)S(C)(=O)=O)ccc1Cl
Show InChI InChI=1S/C22H27ClN2O4S/c1-3-29-21-13-16(7-8-20(21)23)15-25-11-9-18(10-12-25)24-22(26)17-5-4-6-19(14-17)30(2,27)28/h4-8,13-14,18H,3,9-12,15H2,1-2H3,(H,24,26)
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n/an/a 1.30E+3n/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Binding affinity to human ERG channel


J Med Chem 50: 6295-8 (2007)


Article DOI: 10.1021/jm701144e
BindingDB Entry DOI: 10.7270/Q2S18273
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%