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PubMed code 22305493

Compile data set for download or QSAR
Found 33 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
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379308
PNG
(CHEMBL2011816)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C32H36N4O4/c1-22(2)30(31(38)33-24-15-17-35(18-16-24)20-23-9-5-3-6-10-23)36-21-29(37)34-28-14-13-26(19-27(28)32(36)39)40-25-11-7-4-8-12-25/h3-14,19,22,24,30H,15-18,20-21H2,1-2H3,(H,33,38)(H,34,37)/t30-/m1/s1
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4.40n/an/an/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Displacement of [125I]Ghrelin from human GHSR1a receptor


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379328
PNG
(CHEMBL2011825)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccc(F)cc3C)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C33H37FN4O4/c1-21(2)31(32(40)35-25-13-15-37(16-14-25)19-23-7-5-4-6-8-23)38-20-30(39)36-28-11-10-26(18-27(28)33(38)41)42-29-12-9-24(34)17-22(29)3/h4-12,17-18,21,25,31H,13-16,19-20H2,1-3H3,(H,35,40)(H,36,39)/t31-/m1/s1
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n/an/a 0.200n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379309
PNG
(CHEMBL2011826)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3c(C)cccc3C)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C34H40N4O4/c1-22(2)31(33(40)35-26-15-17-37(18-16-26)20-25-11-6-5-7-12-25)38-21-30(39)36-29-14-13-27(19-28(29)34(38)41)42-32-23(3)9-8-10-24(32)4/h5-14,19,22,26,31H,15-18,20-21H2,1-4H3,(H,35,40)(H,36,39)/t31-/m1/s1
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n/an/a 1n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379312
PNG
(CHEMBL2011892)
Show SMILES CC(C)[C@H](C[C@H]1CC[C@H](CC1)NCC1CC1)N1CCCc2ccc(Oc3ccc(F)cc3F)cc2C1=O |r,wU:8.11,5.4,wD:3.17,(36.58,-32.93,;35.81,-34.26,;34.27,-34.25,;36.57,-35.59,;38.11,-35.6,;39.01,-34.36,;38.22,-33.06,;38.97,-31.7,;40.5,-31.69,;41.29,-33,;40.55,-34.34,;41.25,-30.34,;40.46,-29.01,;41.21,-27.66,;42.53,-26.86,;41.18,-26.11,;35.79,-36.92,;36.59,-38.39,;35.93,-39.87,;34.36,-40.25,;33.03,-39.23,;31.7,-40,;30.36,-39.23,;30.36,-37.7,;29.03,-36.94,;27.7,-37.71,;27.71,-39.26,;26.37,-40.03,;25.04,-39.26,;23.7,-40.03,;25.04,-37.72,;26.37,-36.95,;26.36,-35.41,;31.68,-36.92,;33.01,-37.68,;34.24,-36.67,;33.83,-35.18,)|
Show InChI InChI=1S/C31H40F2N2O2/c1-20(2)29(16-21-7-11-25(12-8-21)34-19-22-5-6-22)35-15-3-4-23-9-13-26(18-27(23)31(35)36)37-30-14-10-24(32)17-28(30)33/h9-10,13-14,17-18,20-22,25,29,34H,3-8,11-12,15-16,19H2,1-2H3/t21-,25+,29-/m0/s1
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n/an/a 2n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379320
PNG
(CHEMBL2011834)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)N1CCC(CC1)N[C@H](C)C1CCCCC1 |r|
Show InChI InChI=1S/C33H44N4O4/c1-22(2)31(33(40)36-18-16-25(17-19-36)34-23(3)24-10-6-4-7-11-24)37-21-30(38)35-29-15-14-27(20-28(29)32(37)39)41-26-12-8-5-9-13-26/h5,8-9,12-15,20,22-25,31,34H,4,6-7,10-11,16-19,21H2,1-3H3,(H,35,38)/t23-,31-/m1/s1
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n/an/a 2.5n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379322
PNG
(CHEMBL2011832)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)N1CCC(CC1)N[C@H](C)c1ccccc1 |r|
Show InChI InChI=1S/C33H38N4O4/c1-22(2)31(33(40)36-18-16-25(17-19-36)34-23(3)24-10-6-4-7-11-24)37-21-30(38)35-29-15-14-27(20-28(29)32(37)39)41-26-12-8-5-9-13-26/h4-15,20,22-23,25,31,34H,16-19,21H2,1-3H3,(H,35,38)/t23-,31-/m1/s1
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n/an/a 2.5n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379310
PNG
(CHEMBL2011894)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccc(F)cc3F)cc2C1=O)C(=O)N1CCC(CC1)NCc1ccccc1 |r|
Show InChI InChI=1S/C32H34F2N4O4/c1-20(2)30(32(41)37-14-12-23(13-15-37)35-18-21-6-4-3-5-7-21)38-19-29(39)36-27-10-9-24(17-25(27)31(38)40)42-28-11-8-22(33)16-26(28)34/h3-11,16-17,20,23,30,35H,12-15,18-19H2,1-2H3,(H,36,39)/t30-/m1/s1
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n/an/a 3n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379334
PNG
(CHEMBL2011819)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3C)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C33H38N4O4/c1-22(2)31(32(39)34-25-15-17-36(18-16-25)20-24-10-5-4-6-11-24)37-21-30(38)35-28-14-13-26(19-27(28)33(37)40)41-29-12-8-7-9-23(29)3/h4-14,19,22,25,31H,15-18,20-21H2,1-3H3,(H,34,39)(H,35,38)/t31-/m1/s1
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n/an/a 3n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379319
PNG
(CHEMBL2011835)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)N1CCC(CC1)NCCC1CCCCC1 |r|
Show InChI InChI=1S/C33H44N4O4/c1-23(2)31(33(40)36-19-16-25(17-20-36)34-18-15-24-9-5-3-6-10-24)37-22-30(38)35-29-14-13-27(21-28(29)32(37)39)41-26-11-7-4-8-12-26/h4,7-8,11-14,21,23-25,31,34H,3,5-6,9-10,15-20,22H2,1-2H3,(H,35,38)/t31-/m1/s1
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n/an/a 4.10n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379314
PNG
(CHEMBL2011890)
Show SMILES CC(C)[C@H](C[C@H]1CC[C@H](CC1)NCc1ccccc1)N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O |r,wU:5.4,8.11,wD:3.20,(.88,-6.3,;.11,-7.62,;-1.43,-7.61,;.86,-8.95,;2.4,-8.96,;3.18,-7.63,;2.41,-6.3,;3.2,-4.97,;4.74,-4.98,;5.5,-6.33,;4.72,-7.65,;5.53,-3.65,;7.07,-3.67,;7.83,-5.01,;7.04,-6.33,;7.8,-7.68,;9.34,-7.69,;10.13,-6.35,;9.37,-5.02,;.09,-10.28,;.89,-11.74,;.23,-13.22,;1.27,-14.47,;-1.34,-13.6,;-2.66,-12.58,;-4,-13.35,;-5.33,-12.59,;-5.33,-11.06,;-6.66,-10.29,;-7.99,-11.06,;-9.31,-10.31,;-10.64,-11.07,;-10.64,-12.61,;-9.31,-13.38,;-7.98,-12.61,;-4.01,-10.28,;-2.68,-11.04,;-1.46,-10.03,;-1.86,-8.54,)|
Show InChI InChI=1S/C33H39N3O3/c1-23(2)31(19-24-13-15-26(16-14-24)34-21-25-9-5-3-6-10-25)36-22-32(37)35-30-18-17-28(20-29(30)33(36)38)39-27-11-7-4-8-12-27/h3-12,17-18,20,23-24,26,31,34H,13-16,19,21-22H2,1-2H3,(H,35,37)/t24-,26+,31-/m0/s1
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n/an/a 6n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379311
PNG
(CHEMBL2011893)
Show SMILES CC(C)[C@H](C[C@H]1CC[C@H](CC1)NCC1CC1)N1CCc2ccc(Oc3ccc(F)cc3F)cc2C1=O |r,wU:5.4,8.11,wD:3.17,(13.01,-46.57,;11.68,-47.35,;10.34,-46.58,;11.68,-48.88,;13.01,-49.65,;14.42,-49.01,;14.37,-47.49,;15.69,-46.68,;17.04,-47.43,;17.07,-48.96,;15.76,-49.75,;18.35,-46.62,;18.32,-45.08,;19.64,-44.27,;21.19,-44.23,;20.38,-42.91,;10.35,-49.65,;10.37,-51.2,;9.04,-51.98,;7.7,-51.23,;6.37,-52,;5.03,-51.24,;5.03,-49.7,;3.7,-48.94,;2.37,-49.71,;2.37,-51.26,;1.04,-52.04,;-.3,-51.26,;-1.64,-52.03,;-.29,-49.72,;1.04,-48.95,;1.03,-47.41,;6.35,-48.92,;7.68,-49.68,;9,-48.89,;8.99,-47.35,)|
Show InChI InChI=1S/C30H38F2N2O2/c1-19(2)28(15-20-5-9-24(10-6-20)33-18-21-3-4-21)34-14-13-22-7-11-25(17-26(22)30(34)35)36-29-12-8-23(31)16-27(29)32/h7-8,11-12,16-17,19-21,24,28,33H,3-6,9-10,13-15,18H2,1-2H3/t20-,24+,28-/m0/s1
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n/an/a 7n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379308
PNG
(CHEMBL2011816)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C32H36N4O4/c1-22(2)30(31(38)33-24-15-17-35(18-16-24)20-23-9-5-3-6-10-23)36-21-29(37)34-28-14-13-26(19-27(28)32(36)39)40-25-11-7-4-8-12-25/h3-14,19,22,24,30H,15-18,20-21H2,1-2H3,(H,33,38)(H,34,37)/t30-/m1/s1
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n/an/a 7n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at mouse GHSR1 receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379335
PNG
(CHEMBL2011818)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccc(C)cc3)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C33H38N4O4/c1-22(2)31(32(39)34-25-15-17-36(18-16-25)20-24-7-5-4-6-8-24)37-21-30(38)35-29-14-13-27(19-28(29)33(37)40)41-26-11-9-23(3)10-12-26/h4-14,19,22,25,31H,15-18,20-21H2,1-3H3,(H,34,39)(H,35,38)/t31-/m1/s1
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n/an/a 7n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50153547
PNG
(3-(2,6-Dichloro-phenyl)-5-[2-(2-oxo-piperidin-1-yl...)
Show SMILES CCN(CC)c1ccc(NC(=O)c2c(CCN3CCCCC3=O)onc2-c2c(Cl)cccc2Cl)cc1 |(8.86,-1.12,;7.38,-.65,;6.25,-1.69,;6.56,-3.2,;8.05,-3.65,;4.77,-1.21,;3.64,-2.25,;2.18,-1.77,;1.85,-.28,;.4,.2,;-.75,-.84,;-.42,-2.33,;-2.22,-.36,;-2.7,1.1,;-1.8,2.35,;-2.43,3.77,;-1.53,5.01,;.01,4.83,;.89,6.06,;.28,7.49,;-1.25,7.63,;-2.16,6.39,;-3.7,6.57,;-4.24,1.1,;-4.71,-.37,;-3.45,-1.26,;-3.45,-2.8,;-4.78,-3.58,;-6.13,-2.8,;-4.78,-5.12,;-3.45,-5.88,;-2.11,-5.12,;-2.11,-3.57,;-.58,-3.57,;2.99,.76,;4.44,.3,)|
Show InChI InChI=1S/C27H30Cl2N4O3/c1-3-32(4-2)19-13-11-18(12-14-19)30-27(35)25-22(15-17-33-16-6-5-10-23(33)34)36-31-26(25)24-20(28)8-7-9-21(24)29/h7-9,11-14H,3-6,10,15-17H2,1-2H3,(H,30,35)
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n/an/a 8n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as blockade of intracellular Ca2+ mobilization


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379323
PNG
(CHEMBL2011831)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)N1CCC(CC1)NCc1ccccc1 |r|
Show InChI InChI=1S/C32H36N4O4/c1-22(2)30(32(39)35-17-15-24(16-18-35)33-20-23-9-5-3-6-10-23)36-21-29(37)34-28-14-13-26(19-27(28)31(36)38)40-25-11-7-4-8-12-25/h3-14,19,22,24,30,33H,15-18,20-21H2,1-2H3,(H,34,37)/t30-/m1/s1
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n/an/a 8n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379308
PNG
(CHEMBL2011816)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C32H36N4O4/c1-22(2)30(31(38)33-24-15-17-35(18-16-24)20-23-9-5-3-6-10-23)36-21-29(37)34-28-14-13-26(19-27(28)32(36)39)40-25-11-7-4-8-12-25/h3-14,19,22,24,30H,15-18,20-21H2,1-2H3,(H,33,38)(H,34,37)/t30-/m1/s1
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n/an/a 8n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379336
PNG
(CHEMBL2011817)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccc(F)cc3)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C32H35FN4O4/c1-21(2)30(31(39)34-24-14-16-36(17-15-24)19-22-6-4-3-5-7-22)37-20-29(38)35-28-13-12-26(18-27(28)32(37)40)41-25-10-8-23(33)9-11-25/h3-13,18,21,24,30H,14-17,19-20H2,1-2H3,(H,34,39)(H,35,38)/t30-/m1/s1
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n/an/a 11n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379326
PNG
(CHEMBL2011828)
Show SMILES O=C(NC1CCN(Cc2ccccc2)CC1)[C@@H](C1CC1)N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O |r|
Show InChI InChI=1S/C32H34N4O4/c37-29-21-36(32(39)27-19-26(13-14-28(27)34-29)40-25-9-5-2-6-10-25)30(23-11-12-23)31(38)33-24-15-17-35(18-16-24)20-22-7-3-1-4-8-22/h1-10,13-14,19,23-24,30H,11-12,15-18,20-21H2,(H,33,38)(H,34,37)/t30-/m1/s1
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n/an/a 12n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50158327
PNG
((+/-)isobutyl 2-((4-(diethylamino)phenyl)carbamoyl...)
Show SMILES CCN(CC)c1ccc(NC(=O)C2(CCc3cccc(OC)c3C2)N(C)C(=O)OCC(C)C)cc1
Show InChI InChI=1S/C28H39N3O4/c1-7-31(8-2)23-14-12-22(13-15-23)29-26(32)28(30(5)27(33)35-19-20(3)4)17-16-21-10-9-11-25(34-6)24(21)18-28/h9-15,20H,7-8,16-19H2,1-6H3,(H,29,32)
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n/an/a 16n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as blockade of intracellular Ca2+ mobilization


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379321
PNG
(CHEMBL2011833)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)N1CCC(CC1)NC(C)(C)c1ccccc1 |r|
Show InChI InChI=1S/C34H40N4O4/c1-23(2)31(33(41)37-19-17-25(18-20-37)36-34(3,4)24-11-7-5-8-12-24)38-22-30(39)35-29-16-15-27(21-28(29)32(38)40)42-26-13-9-6-10-14-26/h5-16,21,23,25,31,36H,17-20,22H2,1-4H3,(H,35,39)/t31-/m1/s1
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n/an/a 16.5n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379313
PNG
(CHEMBL2011891)
Show SMILES CC(C)[C@H](C[C@H]1CC[C@H](CC1)NCC1CC1)N1CC(=O)Nc2ccc(Oc3ccc(F)cc3F)cc2C1=O |r,wU:8.11,5.4,wD:3.17,(17.11,-33.7,;16.33,-35.03,;14.8,-35.02,;17.09,-36.36,;18.63,-36.37,;19.54,-35.12,;18.74,-33.82,;19.49,-32.47,;21.03,-32.45,;21.82,-33.77,;21.07,-35.1,;21.78,-31.11,;20.98,-29.78,;21.73,-28.43,;23.06,-27.63,;21.7,-26.87,;16.32,-37.69,;17.12,-39.15,;16.45,-40.64,;17.5,-41.89,;14.88,-41.02,;13.56,-40,;12.22,-40.77,;10.88,-40,;10.88,-38.47,;9.55,-37.7,;8.22,-38.47,;8.23,-40.02,;6.9,-40.8,;5.56,-40.02,;4.22,-40.79,;5.57,-38.49,;6.89,-37.72,;6.89,-36.17,;12.21,-37.69,;13.54,-38.45,;14.76,-37.43,;14.36,-35.95,)|
Show InChI InChI=1S/C30H37F2N3O3/c1-18(2)27(13-19-5-8-22(9-6-19)33-16-20-3-4-20)35-17-29(36)34-26-11-10-23(15-24(26)30(35)37)38-28-12-7-21(31)14-25(28)32/h7,10-12,14-15,18-20,22,27,33H,3-6,8-9,13,16-17H2,1-2H3,(H,34,36)/t19-,22+,27-/m0/s1
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n/an/a 20n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379331
PNG
(CHEMBL2011822)
Show SMILES COc1ccccc1Oc1ccc2NC(=O)CN([C@H](C(C)C)C(=O)NC3CCN(Cc4ccccc4)CC3)C(=O)c2c1 |r|
Show InChI InChI=1S/C33H38N4O5/c1-22(2)31(32(39)34-24-15-17-36(18-16-24)20-23-9-5-4-6-10-23)37-21-30(38)35-27-14-13-25(19-26(27)33(37)40)42-29-12-8-7-11-28(29)41-3/h4-14,19,22,24,31H,15-18,20-21H2,1-3H3,(H,34,39)(H,35,38)/t31-/m1/s1
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n/an/a 26n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379332
PNG
(CHEMBL2011821)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccc(Cl)cc3)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C32H35ClN4O4/c1-21(2)30(31(39)34-24-14-16-36(17-15-24)19-22-6-4-3-5-7-22)37-20-29(38)35-28-13-12-26(18-27(28)32(37)40)41-25-10-8-23(33)9-11-25/h3-13,18,21,24,30H,14-17,19-20H2,1-2H3,(H,34,39)(H,35,38)/t30-/m1/s1
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n/an/a 28n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379317
PNG
(CHEMBL2011887)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)N1CCC(CC1)NCC1CC1 |r|
Show InChI InChI=1S/C29H36N4O4/c1-19(2)27(29(36)32-14-12-21(13-15-32)30-17-20-8-9-20)33-18-26(34)31-25-11-10-23(16-24(25)28(33)35)37-22-6-4-3-5-7-22/h3-7,10-11,16,19-21,27,30H,8-9,12-15,17-18H2,1-2H3,(H,31,34)/t27-/m1/s1
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n/an/a 50n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379329
PNG
(CHEMBL2011824)
Show SMILES COc1ccc(Oc2ccc3NC(=O)CN([C@H](C(C)C)C(=O)NC4CCN(Cc5ccccc5)CC4)C(=O)c3c2)cc1 |r|
Show InChI InChI=1S/C33H38N4O5/c1-22(2)31(32(39)34-24-15-17-36(18-16-24)20-23-7-5-4-6-8-23)37-21-30(38)35-29-14-13-27(19-28(29)33(37)40)42-26-11-9-25(41-3)10-12-26/h4-14,19,22,24,31H,15-18,20-21H2,1-3H3,(H,34,39)(H,35,38)/t31-/m1/s1
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n/an/a 79n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379330
PNG
(CHEMBL2011823)
Show SMILES COc1cccc(Oc2ccc3NC(=O)CN([C@H](C(C)C)C(=O)NC4CCN(Cc5ccccc5)CC4)C(=O)c3c2)c1 |r|
Show InChI InChI=1S/C33H38N4O5/c1-22(2)31(32(39)34-24-14-16-36(17-15-24)20-23-8-5-4-6-9-23)37-21-30(38)35-29-13-12-27(19-28(29)33(37)40)42-26-11-7-10-25(18-26)41-3/h4-13,18-19,22,24,31H,14-17,20-21H2,1-3H3,(H,34,39)(H,35,38)/t31-/m1/s1
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n/an/a 143n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379333
PNG
(CHEMBL2011820)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3cccc(Cl)c3)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C32H35ClN4O4/c1-21(2)30(31(39)34-24-13-15-36(16-14-24)19-22-7-4-3-5-8-22)37-20-29(38)35-28-12-11-26(18-27(28)32(37)40)41-25-10-6-9-23(33)17-25/h3-12,17-18,21,24,30H,13-16,19-20H2,1-2H3,(H,34,39)(H,35,38)/t30-/m1/s1
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n/an/a 171n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379325
PNG
(CHEMBL2011829)
Show SMILES CC(C)[C@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)NC1CCN(Cc2ccccc2)CC1 |r|
Show InChI InChI=1S/C32H36N4O4/c1-22(2)30(31(38)33-24-15-17-35(18-16-24)20-23-9-5-3-6-10-23)36-21-29(37)34-28-14-13-26(19-27(28)32(36)39)40-25-11-7-4-8-12-25/h3-14,19,22,24,30H,15-18,20-21H2,1-2H3,(H,33,38)(H,34,37)/t30-/m0/s1
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n/an/a 196n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379318
PNG
(CHEMBL2011836)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)N1CCC(CC1)NCCC1CCOCC1 |r|
Show InChI InChI=1S/C32H42N4O5/c1-22(2)30(32(39)35-16-11-24(12-17-35)33-15-10-23-13-18-40-19-14-23)36-21-29(37)34-28-9-8-26(20-27(28)31(36)38)41-25-6-4-3-5-7-25/h3-9,20,22-24,30,33H,10-19,21H2,1-2H3,(H,34,37)/t30-/m1/s1
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n/an/a 313n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379327
PNG
(CHEMBL2011827)
Show SMILES O=C(CN1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)NC1CCN(Cc2ccccc2)CC1
Show InChI InChI=1S/C29H30N4O4/c34-27(30-22-13-15-32(16-14-22)18-21-7-3-1-4-8-21)19-33-20-28(35)31-26-12-11-24(17-25(26)29(33)36)37-23-9-5-2-6-10-23/h1-12,17,22H,13-16,18-20H2,(H,30,34)(H,31,35)
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n/an/a 314n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379316
PNG
(CHEMBL2011888)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)NC1CCNCC1 |r|
Show InChI InChI=1S/C25H30N4O4/c1-16(2)23(24(31)27-17-10-12-26-13-11-17)29-15-22(30)28-21-9-8-19(14-20(21)25(29)32)33-18-6-4-3-5-7-18/h3-9,14,16-17,23,26H,10-13,15H2,1-2H3,(H,27,31)(H,28,30)/t23-/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379324
PNG
(CHEMBL2011830)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)NC1CCC(Cc2ccccc2)CC1 |r,wD:3.3,(44.28,7.98,;43.51,6.64,;41.97,6.65,;44.26,5.32,;43.49,3.99,;44.29,2.53,;43.62,1.05,;44.66,-.2,;42.06,.67,;40.73,1.68,;39.4,.92,;38.06,1.68,;38.07,3.21,;36.74,3.98,;35.41,3.2,;34.08,3.96,;32.76,3.19,;32.76,1.66,;34.09,.89,;35.42,1.66,;39.38,3.99,;40.71,3.23,;41.94,4.24,;41.53,5.73,;45.8,5.31,;46.56,3.98,;46.57,6.63,;48.11,6.63,;48.87,5.29,;50.41,5.28,;51.19,6.61,;52.73,6.6,;53.51,7.94,;55.05,7.92,;55.83,9.25,;55.07,10.59,;53.52,10.6,;52.75,9.27,;50.42,7.97,;48.87,7.97,)|
Show InChI InChI=1S/C33H37N3O4/c1-22(2)31(32(38)34-25-15-13-24(14-16-25)19-23-9-5-3-6-10-23)36-21-30(37)35-29-18-17-27(20-28(29)33(36)39)40-26-11-7-4-8-12-26/h3-12,17-18,20,22,24-25,31H,13-16,19,21H2,1-2H3,(H,34,38)(H,35,37)/t24?,25?,31-/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
Growth hormone secretagogue receptor type 1


(Homo sapiens (Human))
BDBM50379315
PNG
(CHEMBL2011889)
Show SMILES CC(C)[C@@H](N1CC(=O)Nc2ccc(Oc3ccccc3)cc2C1=O)C(=O)NC1CCN(CC1)C(=O)c1ccccc1 |r|
Show InChI InChI=1S/C32H34N4O5/c1-21(2)29(30(38)33-23-15-17-35(18-16-23)31(39)22-9-5-3-6-10-22)36-20-28(37)34-27-14-13-25(19-26(27)32(36)40)41-24-11-7-4-8-12-24/h3-14,19,21,23,29H,15-18,20H2,1-2H3,(H,33,38)(H,34,37)/t29-/m1/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Amgen Inc.

Curated by ChEMBL


Assay Description
Antagonist activity at human GHSR1a receptor assessed as intracellular Ca2+ concentration by aequorin luminescent assay


Bioorg Med Chem Lett 22: 2046-51 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.014
BindingDB Entry DOI: 10.7270/Q21J9BRV
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%