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Compile Data Set for Download or QSAR

Found 100 hits Enz. Inhib. hit(s) with all data for entry = 50049185   
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
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235937
PNG
(CHEMBL4095917)
Show SMILES CN1CCN(CC1)n1c2ccc(\C=C3/c4ccccc4COc4cc(F)ccc34)cc2[nH]c1=NC#N
Show InChI InChI=1S/C28H25FN6O/c1-33-10-12-34(13-11-33)35-26-9-6-19(15-25(26)32-28(35)31-18-30)14-24-22-5-3-2-4-20(22)17-36-27-16-21(29)7-8-23(24)27/h2-9,14-16H,10-13,17H2,1H3,(H,31,32)/b24-14+
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0.0800n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-Aldosterone from MR overexpressed in human 293 cells measured after 2 hrs by Microbeta scintillation counting method


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235934
PNG
(CHEMBL4086416)
Show SMILES [H][C@]12C[C@@H](CN1CCOC2)n1c2ccc(\C=C3\c4ccc(F)cc4OCc4c(F)cccc34)cc2[nH]c1=NC#N |r|
Show InChI InChI=1S/C30H25F2N5O2/c31-19-5-6-23-24(22-2-1-3-26(32)25(22)16-39-29(23)12-19)10-18-4-7-28-27(11-18)35-30(34-17-33)37(28)20-13-21-15-38-9-8-36(21)14-20/h1-7,10-12,20-21H,8-9,13-16H2,(H,34,35)/b24-10+/t20-,21+/m0/s1
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0.230n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-Aldosterone from MR overexpressed in human 293 cells measured after 2 hrs by Microbeta scintillation counting method


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235935
PNG
(CHEMBL4088896)
Show SMILES C[C@H](CN1CCOCC1)n1c2ccc(\C=C3/c4ccccc4COc4cc(F)ccc34)cc2[nH]c1=NC(N)=O |r|
Show InChI InChI=1S/C30H30FN5O3/c1-19(17-35-10-12-38-13-11-35)36-27-9-6-20(15-26(27)33-30(36)34-29(32)37)14-25-23-5-3-2-4-21(23)18-39-28-16-22(31)7-8-24(25)28/h2-9,14-16,19H,10-13,17-18H2,1H3,(H3,32,33,34,37)/b25-14+/t19-/m1/s1
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0.330n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-Aldosterone from MR overexpressed in human 293 cells measured after 2 hrs by Microbeta scintillation counting method


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235936
PNG
(CHEMBL4099276)
Show SMILES C[C@H](CN1CCOCC1)n1c2ccc(\C=C3/c4ccccc4COc4cc(F)ccc34)cc2[nH]c1=NC#N |r|
Show InChI InChI=1S/C30H28FN5O2/c1-20(17-35-10-12-37-13-11-35)36-28-9-6-21(15-27(28)34-30(36)33-19-32)14-26-24-5-3-2-4-22(24)18-38-29-16-23(31)7-8-25(26)29/h2-9,14-16,20H,10-13,17-18H2,1H3,(H,33,34)/b26-14+/t20-/m1/s1
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0.400n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-Aldosterone from MR overexpressed in human 293 cells measured after 2 hrs by Microbeta scintillation counting method


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235981
PNG
(CHEMBL4063735)
Show SMILES C[C@H](CN1CCOCC1)n1c2ccc(\C=C3/c4ccc(F)cc4COc4cc(F)ccc34)cc2[nH]c1=NC#N |r|
Show InChI InChI=1S/C30H27F2N5O2/c1-19(16-36-8-10-38-11-9-36)37-28-7-2-20(13-27(28)35-30(37)34-18-33)12-26-24-5-3-22(31)14-21(24)17-39-29-15-23(32)4-6-25(26)29/h2-7,12-15,19H,8-11,16-17H2,1H3,(H,34,35)/b26-12+/t19-/m1/s1
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0.790n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-Aldosterone from MR overexpressed in human 293 cells measured after 2 hrs by Microbeta scintillation counting method


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50154362
PNG
(CHEMBL3775798)
Show SMILES [H][C@]12C[C@H](CN1CCOC2)n1c2ccc(\C=C3/c4ccccc4COc4cc(F)ccc34)cc2[nH]c1=O |r|
Show InChI InChI=1S/C29H26FN3O3/c30-20-6-7-24-25(23-4-2-1-3-19(23)16-36-28(24)13-20)11-18-5-8-27-26(12-18)31-29(34)33(27)21-14-22-17-35-10-9-32(22)15-21/h1-8,11-13,21-22H,9-10,14-17H2,(H,31,34)/b25-11+/t21-,22-/m1/s1
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9n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Compound was tested for its ability to stimulate [35S]GTP-gamma-S, binding to membranes from C6 glioma cells stably expressing rat mu opioid receptor


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235933
PNG
(CHEMBL3775714)
Show SMILES Fc1ccc2c(OCc3ccccc3\C2=C/c2ccc3[nH]c(=O)[nH]c3c2)c1
Show InChI InChI=1S/C22H15FN2O2/c23-15-6-7-17-18(9-13-5-8-19-20(10-13)25-22(26)24-19)16-4-2-1-3-14(16)12-27-21(17)11-15/h1-11H,12H2,(H2,24,25,26)/b18-9+
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12n/an/an/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-cortisol from MR overexpressed in human 293 cells measured after 2 hrs by Microbeta scintillation counting method


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235931
PNG
(CHEMBL4087205)
Show SMILES C[C@H](O)Cc1cc(C(=O)Nc2ccc(cc2)S(C)(=O)=O)c(C)n1-c1ccc(Cl)cc1-c1ccc(F)cc1 |r,wU:1.0,(29.96,-24.22,;31.49,-24.07,;32.39,-25.31,;32.12,-22.66,;31.21,-21.41,;29.67,-21.41,;29.2,-19.95,;27.74,-19.47,;27.42,-17.97,;26.59,-20.5,;25.13,-20.03,;24.82,-18.52,;23.35,-18.04,;22.21,-19.08,;22.53,-20.59,;24,-21.06,;20.74,-18.6,;19.6,-19.64,;19.96,-17.26,;21.51,-17.25,;30.44,-19.04,;30.44,-17.5,;31.69,-19.95,;33.16,-19.47,;34.29,-20.51,;35.76,-20.03,;36.08,-18.53,;37.55,-18.05,;34.93,-17.49,;33.47,-17.97,;32.32,-16.95,;32.64,-15.44,;31.5,-14.42,;30.03,-14.9,;28.88,-13.87,;29.72,-16.42,;30.87,-17.43,)|
Show InChI InChI=1S/C28H26ClFN2O4S/c1-17(33)14-23-16-25(28(34)31-22-9-11-24(12-10-22)37(3,35)36)18(2)32(23)27-13-6-20(29)15-26(27)19-4-7-21(30)8-5-19/h4-13,15-17,33H,14H2,1-3H3,(H,31,34)/t17-/m0/s1
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n/an/a 1.20n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (671 to 984 residues) expressed in African Green Monkey CV-1 cells assessed as inhibition of aldostero...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235931
PNG
(CHEMBL4087205)
Show SMILES C[C@H](O)Cc1cc(C(=O)Nc2ccc(cc2)S(C)(=O)=O)c(C)n1-c1ccc(Cl)cc1-c1ccc(F)cc1 |r,wU:1.0,(29.96,-24.22,;31.49,-24.07,;32.39,-25.31,;32.12,-22.66,;31.21,-21.41,;29.67,-21.41,;29.2,-19.95,;27.74,-19.47,;27.42,-17.97,;26.59,-20.5,;25.13,-20.03,;24.82,-18.52,;23.35,-18.04,;22.21,-19.08,;22.53,-20.59,;24,-21.06,;20.74,-18.6,;19.6,-19.64,;19.96,-17.26,;21.51,-17.25,;30.44,-19.04,;30.44,-17.5,;31.69,-19.95,;33.16,-19.47,;34.29,-20.51,;35.76,-20.03,;36.08,-18.53,;37.55,-18.05,;34.93,-17.49,;33.47,-17.97,;32.32,-16.95,;32.64,-15.44,;31.5,-14.42,;30.03,-14.9,;28.88,-13.87,;29.72,-16.42,;30.87,-17.43,)|
Show InChI InChI=1S/C28H26ClFN2O4S/c1-17(33)14-23-16-25(28(34)31-22-9-11-24(12-10-22)37(3,35)36)18(2)32(23)27-13-6-20(29)15-26(27)19-4-7-21(30)8-5-19/h4-13,15-17,33H,14H2,1-3H3,(H,31,34)/t17-/m0/s1
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n/an/a 1.20n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (671 to 984 residues) expressed in African Green Monkey CV-1 cells assessed as inhibition of aldostero...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235961
PNG
(CHEMBL4102708)
Show SMILES CC(=O)Oc1ccc(CCc2cc(C)c3OCC(=O)Nc3c2)c(C)c1
Show InChI InChI=1S/C20H21NO4/c1-12-9-17(25-14(3)22)7-6-16(12)5-4-15-8-13(2)20-18(10-15)21-19(23)11-24-20/h6-10H,4-5,11H2,1-3H3,(H,21,23)
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n/an/a 1.30n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Inhibition of rat liver KYN 3-OHase.


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235960
PNG
(CHEMBL4078451)
Show SMILES CC(=O)Oc1ccc(CCc2ccc3OCC(=O)Nc3c2)c(C)c1
Show InChI InChI=1S/C19H19NO4/c1-12-9-16(24-13(2)21)7-6-15(12)5-3-14-4-8-18-17(10-14)20-19(22)11-23-18/h4,6-10H,3,5,11H2,1-2H3,(H,20,22)
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n/an/a<2n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (672 to 984 residues) expressed in HEK293T cells assessed as inhibition of aldosterone-induced transac...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235932
PNG
(CHEMBL4065788)
Show SMILES C[C@H](O)Cc1cc(C(=O)Nc2ccc(cc2)S(C)(=O)=O)c(C)n1-c1ccc(Cl)cc1C(F)(F)F |r,wU:1.0,(10.44,-22.82,;11.97,-22.66,;12.88,-23.9,;12.6,-21.25,;11.7,-20,;10.16,-20,;9.69,-18.54,;8.22,-18.07,;7.9,-16.56,;7.08,-19.1,;5.61,-18.62,;5.3,-17.11,;3.84,-16.64,;2.69,-17.67,;3.02,-19.18,;4.48,-19.65,;1.22,-17.19,;.08,-18.23,;.44,-15.85,;1.99,-15.85,;10.93,-17.63,;10.93,-16.09,;12.18,-18.54,;13.64,-18.07,;14.78,-19.1,;16.24,-18.63,;16.57,-17.12,;18.03,-16.64,;15.41,-16.09,;13.95,-16.56,;12.81,-15.54,;13.12,-14.03,;11.34,-16.02,;11.71,-14.44,)|
Show InChI InChI=1S/C23H22ClF3N2O4S/c1-13(30)10-17-12-19(22(31)28-16-5-7-18(8-6-16)34(3,32)33)14(2)29(17)21-9-4-15(24)11-20(21)23(25,26)27/h4-9,11-13,30H,10H2,1-3H3,(H,28,31)/t13-/m0/s1
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n/an/a 3.10n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (671 to 984 residues) expressed in African Green Monkey CV-1 cells assessed as inhibition of aldostero...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235932
PNG
(CHEMBL4065788)
Show SMILES C[C@H](O)Cc1cc(C(=O)Nc2ccc(cc2)S(C)(=O)=O)c(C)n1-c1ccc(Cl)cc1C(F)(F)F |r,wU:1.0,(10.44,-22.82,;11.97,-22.66,;12.88,-23.9,;12.6,-21.25,;11.7,-20,;10.16,-20,;9.69,-18.54,;8.22,-18.07,;7.9,-16.56,;7.08,-19.1,;5.61,-18.62,;5.3,-17.11,;3.84,-16.64,;2.69,-17.67,;3.02,-19.18,;4.48,-19.65,;1.22,-17.19,;.08,-18.23,;.44,-15.85,;1.99,-15.85,;10.93,-17.63,;10.93,-16.09,;12.18,-18.54,;13.64,-18.07,;14.78,-19.1,;16.24,-18.63,;16.57,-17.12,;18.03,-16.64,;15.41,-16.09,;13.95,-16.56,;12.81,-15.54,;13.12,-14.03,;11.34,-16.02,;11.71,-14.44,)|
Show InChI InChI=1S/C23H22ClF3N2O4S/c1-13(30)10-17-12-19(22(31)28-16-5-7-18(8-6-16)34(3,32)33)14(2)29(17)21-9-4-15(24)11-20(21)23(25,26)27/h4-9,11-13,30H,10H2,1-3H3,(H,28,31)/t13-/m0/s1
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n/an/a 3.10n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (671 to 984 residues) expressed in African Green Monkey CV-1 cells assessed as inhibition of aldostero...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235959
PNG
(CHEMBL4064750)
Show SMILES Cc1c(cc(CCO)n1-c1ccc(Cl)cc1C(F)(F)F)C(=O)Nc1ccc(cc1)S(C)(=O)=O |(72.44,-4.78,;72.44,-6.32,;71.2,-7.22,;71.67,-8.69,;73.21,-8.69,;74.12,-9.93,;73.49,-11.34,;74.39,-12.59,;73.69,-7.22,;75.16,-6.75,;76.29,-7.78,;77.76,-7.31,;78.08,-5.8,;79.55,-5.33,;76.93,-4.77,;75.47,-5.25,;74.32,-4.22,;74.64,-2.71,;72.86,-4.7,;73.22,-3.12,;69.74,-6.75,;69.42,-5.24,;68.59,-7.78,;67.13,-7.3,;66.82,-5.8,;65.35,-5.32,;64.21,-6.35,;64.54,-7.86,;66,-8.33,;62.74,-5.87,;61.6,-6.91,;61.96,-4.53,;63.51,-4.53,)|
Show InChI InChI=1S/C22H20ClF3N2O4S/c1-13-18(21(30)27-15-4-6-17(7-5-15)33(2,31)32)12-16(9-10-29)28(13)20-8-3-14(23)11-19(20)22(24,25)26/h3-8,11-12,29H,9-10H2,1-2H3,(H,27,30)
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n/an/a 3.70n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Stimulation of cAMP in CHO cells expressing human m2 receptor


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235959
PNG
(CHEMBL4064750)
Show SMILES Cc1c(cc(CCO)n1-c1ccc(Cl)cc1C(F)(F)F)C(=O)Nc1ccc(cc1)S(C)(=O)=O |(72.44,-4.78,;72.44,-6.32,;71.2,-7.22,;71.67,-8.69,;73.21,-8.69,;74.12,-9.93,;73.49,-11.34,;74.39,-12.59,;73.69,-7.22,;75.16,-6.75,;76.29,-7.78,;77.76,-7.31,;78.08,-5.8,;79.55,-5.33,;76.93,-4.77,;75.47,-5.25,;74.32,-4.22,;74.64,-2.71,;72.86,-4.7,;73.22,-3.12,;69.74,-6.75,;69.42,-5.24,;68.59,-7.78,;67.13,-7.3,;66.82,-5.8,;65.35,-5.32,;64.21,-6.35,;64.54,-7.86,;66,-8.33,;62.74,-5.87,;61.6,-6.91,;61.96,-4.53,;63.51,-4.53,)|
Show InChI InChI=1S/C22H20ClF3N2O4S/c1-13-18(21(30)27-15-4-6-17(7-5-15)33(2,31)32)12-16(9-10-29)28(13)20-8-3-14(23)11-19(20)22(24,25)26/h3-8,11-12,29H,9-10H2,1-2H3,(H,27,30)
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n/an/a 3.70n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (671 to 984 residues) expressed in African Green Monkey CV-1 cells assessed as inhibition of aldostero...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235944
PNG
(CHEMBL4078631)
Show SMILES C[C@H](O)[C@@H](C)n1cc(C(=O)Nc2ccc(cc2)S(C)(=O)=O)c(C)c1-c1ccc(F)cc1C(F)(F)F |r,wU:1.0,wD:3.3,(67.48,-25.05,;69.02,-24.89,;69.92,-26.14,;69.64,-23.48,;71.18,-23.32,;68.74,-22.24,;67.2,-22.24,;66.73,-20.77,;65.26,-20.3,;64.94,-18.79,;64.12,-21.33,;62.66,-20.85,;62.34,-19.34,;60.88,-18.87,;59.74,-19.9,;60.06,-21.41,;61.53,-21.88,;58.26,-19.42,;57.13,-20.46,;57.49,-18.08,;59.03,-18.08,;67.97,-19.86,;67.97,-18.32,;69.22,-20.77,;70.69,-20.3,;71.82,-21.33,;73.29,-20.86,;73.61,-19.35,;75.07,-18.88,;72.46,-18.32,;71,-18.8,;69.85,-17.77,;70.16,-16.26,;68.39,-18.25,;68.75,-16.67,)|
Show InChI InChI=1S/C24H24F4N2O4S/c1-13-20(23(32)29-17-6-8-18(9-7-17)35(4,33)34)12-30(14(2)15(3)31)22(13)19-10-5-16(25)11-21(19)24(26,27)28/h5-12,14-15,31H,1-4H3,(H,29,32)/t14-,15+/m1/s1
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n/an/a 3.80n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Compound was tested in vitro for inhibition of tubulin polymerization.


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM121444
PNG
(US8722709, 48)
Show SMILES Cc1cc(F)ccc1CCc1ccnc(NC(N)=O)c1
Show InChI InChI=1S/C15H16FN3O/c1-10-8-13(16)5-4-12(10)3-2-11-6-7-18-14(9-11)19-15(17)20/h4-9H,2-3H2,1H3,(H3,17,18,19,20)
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n/an/a 4.70n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of TAMRA-labeled dexamethasone from full-length human mineralocorticoid receptor expressed in baculovirus infected insect cells after 60...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235965
PNG
(CHEMBL4088459)
Show SMILES C[C@H](O)[C@@H](C)c1cc(C(=O)Nc2ccc(cc2)S(C)(=O)=O)c(C)n1-c1ccc(F)cc1C(F)(F)F |r,wU:1.0,wD:3.3,(68.05,-24.81,;69.58,-24.65,;70.49,-25.9,;70.21,-23.24,;71.74,-23.08,;69.31,-22,;67.77,-22,;67.3,-20.53,;65.83,-20.06,;65.51,-18.55,;64.69,-21.09,;63.22,-20.61,;62.91,-19.1,;61.45,-18.63,;60.3,-19.66,;60.63,-21.17,;62.09,-21.64,;58.83,-19.18,;57.69,-20.22,;58.05,-17.84,;59.6,-17.84,;68.54,-19.62,;68.54,-18.08,;69.79,-20.53,;71.25,-20.06,;72.39,-21.09,;73.85,-20.62,;74.18,-19.11,;75.64,-18.63,;73.02,-18.08,;71.56,-18.56,;70.42,-17.53,;70.73,-16.02,;68.95,-18.01,;69.32,-16.43,)|
Show InChI InChI=1S/C24H24F4N2O4S/c1-13(15(3)31)22-12-19(23(32)29-17-6-8-18(9-7-17)35(4,33)34)14(2)30(22)21-10-5-16(25)11-20(21)24(26,27)28/h5-13,15,31H,1-4H3,(H,29,32)/t13-,15+/m1/s1
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n/an/a 6.20n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (671 to 984 residues) expressed in African Green Monkey CV-1 cells assessed as inhibition of aldostero...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235945
PNG
(CHEMBL4068898)
Show SMILES Cc1c(cc(CCF)n1-c1ccc(F)cc1OC(F)F)C(=O)Nc1ccc(cc1)S(C)(=O)=O |(49.68,-18.43,;49.68,-19.97,;48.44,-20.87,;48.91,-22.34,;50.45,-22.34,;51.35,-23.59,;50.72,-24.99,;51.63,-26.24,;50.93,-20.87,;52.39,-20.4,;53.53,-21.43,;54.99,-20.96,;55.32,-19.45,;56.78,-18.98,;54.16,-18.42,;52.7,-18.9,;51.56,-17.87,;51.87,-16.36,;50.72,-15.34,;53.33,-15.88,;46.97,-20.4,;46.65,-18.89,;45.83,-21.43,;44.36,-20.95,;44.05,-19.45,;42.59,-18.97,;41.44,-20,;41.77,-21.51,;43.23,-21.98,;39.97,-19.52,;38.83,-20.56,;39.19,-18.18,;40.74,-18.18,)|
Show InChI InChI=1S/C22H20F4N2O4S/c1-13-18(21(29)27-15-4-6-17(7-5-15)33(2,30)31)12-16(9-10-23)28(13)19-8-3-14(24)11-20(19)32-22(25)26/h3-8,11-12,22H,9-10H2,1-2H3,(H,27,29)
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n/an/a 6.5n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (671 to 984 residues) expressed in African Green Monkey CV-1 cells assessed as inhibition of aldostero...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235945
PNG
(CHEMBL4068898)
Show SMILES Cc1c(cc(CCF)n1-c1ccc(F)cc1OC(F)F)C(=O)Nc1ccc(cc1)S(C)(=O)=O |(49.68,-18.43,;49.68,-19.97,;48.44,-20.87,;48.91,-22.34,;50.45,-22.34,;51.35,-23.59,;50.72,-24.99,;51.63,-26.24,;50.93,-20.87,;52.39,-20.4,;53.53,-21.43,;54.99,-20.96,;55.32,-19.45,;56.78,-18.98,;54.16,-18.42,;52.7,-18.9,;51.56,-17.87,;51.87,-16.36,;50.72,-15.34,;53.33,-15.88,;46.97,-20.4,;46.65,-18.89,;45.83,-21.43,;44.36,-20.95,;44.05,-19.45,;42.59,-18.97,;41.44,-20,;41.77,-21.51,;43.23,-21.98,;39.97,-19.52,;38.83,-20.56,;39.19,-18.18,;40.74,-18.18,)|
Show InChI InChI=1S/C22H20F4N2O4S/c1-13-18(21(29)27-15-4-6-17(7-5-15)33(2,30)31)12-16(9-10-23)28(13)19-8-3-14(24)11-20(19)32-22(25)26/h3-8,11-12,22H,9-10H2,1-2H3,(H,27,29)
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n/an/a 6.5n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
compound was evaluated for inhibition of rat liver KYN 3-OHase.


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235953
PNG
(CHEMBL4104632)
Show SMILES CC(=O)C1=C(C)NC(C)=C([C@@H]1c1cccc2c1oc(C)cc2=O)C(=O)OC1CCC1 |r,c:3,8|
Show InChI InChI=1S/C24H25NO5/c1-12-11-19(27)17-9-6-10-18(23(17)29-12)22-20(15(4)26)13(2)25-14(3)21(22)24(28)30-16-7-5-8-16/h6,9-11,16,22,25H,5,7-8H2,1-4H3/t22-/m1/s1
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n/an/a 7n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (734 to 985 residues) expressed in CHO-K1 cells after 5 to 6 hrs by luciferase reporter gene assay


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50398058
PNG
(CHEMBL2181933 | US8722709, 24)
Show SMILES Cc1ccccc1CCc1ccnc(NC(N)=O)c1
Show InChI InChI=1S/C15H17N3O/c1-11-4-2-3-5-13(11)7-6-12-8-9-17-14(10-12)18-15(16)19/h2-5,8-10H,6-7H2,1H3,(H3,16,17,18,19)
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n/an/a 7.10n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of TAMRA-labeled dexamethasone from full-length human mineralocorticoid receptor expressed in baculovirus infected insect cells after 60...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM121413
PNG
(US8722709, 16)
Show SMILES NC(=O)Nc1cc(ccn1)-c1ccnn1-c1ccc(Cl)cc1
Show InChI InChI=1S/C15H12ClN5O/c16-11-1-3-12(4-2-11)21-13(6-8-19-21)10-5-7-18-14(9-10)20-15(17)22/h1-9H,(H3,17,18,20,22)
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n/an/a 9.40n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of TAMRA-labeled dexamethasone from full-length human mineralocorticoid receptor expressed in baculovirus infected insect cells after 60...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50398059
PNG
(CHEMBL2181932)
Show SMILES Cc1c(cn(CCO)c1-c1ccccc1C(F)(F)F)C(=O)Nc1ccc(cc1)S(C)(=O)=O |(34.95,-31.12,;34.48,-32.58,;33,-33.06,;33.01,-34.59,;34.47,-35.07,;34.85,-36.57,;33.75,-37.64,;34.13,-39.14,;35.38,-33.82,;36.92,-33.83,;37.69,-32.5,;39.22,-32.5,;40,-33.83,;39.22,-35.17,;37.68,-35.17,;36.92,-36.49,;35.38,-36.49,;37.68,-37.83,;36.13,-37.83,;31.76,-32.15,;31.76,-30.61,;30.43,-32.92,;29.09,-32.16,;27.76,-32.93,;26.42,-32.16,;26.42,-30.61,;27.75,-29.84,;29.08,-30.6,;25.09,-29.84,;25.08,-28.3,;24.31,-31.17,;23.55,-29.84,)|
Show InChI InChI=1S/C22H21F3N2O4S/c1-14-18(21(29)26-15-7-9-16(10-8-15)32(2,30)31)13-27(11-12-28)20(14)17-5-3-4-6-19(17)22(23,24)25/h3-10,13,28H,11-12H2,1-2H3,(H,26,29)
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n/an/a 9.40n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (671 to 984 residues) expressed in African Green Monkey CV-1 cells assessed as inhibition of aldostero...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM121428
PNG
(US8722709, 32)
Show SMILES CC(Cc1ccnc(NC(N)=O)c1)c1ccccc1C
Show InChI InChI=1S/C16H19N3O/c1-11-5-3-4-6-14(11)12(2)9-13-7-8-18-15(10-13)19-16(17)20/h3-8,10,12H,9H2,1-2H3,(H3,17,18,19,20)
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n/an/a 11n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of TAMRA-labeled dexamethasone from full-length human mineralocorticoid receptor expressed in baculovirus infected insect cells after 60...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM121427
PNG
(US8722709, 31)
Show SMILES NC(=O)Nc1cc(CC(c2ccccc2)c2ccccc2)ccn1
Show InChI InChI=1S/C20H19N3O/c21-20(24)23-19-14-15(11-12-22-19)13-18(16-7-3-1-4-8-16)17-9-5-2-6-10-17/h1-12,14,18H,13H2,(H3,21,22,23,24)
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n/an/a 13n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of TAMRA-labeled dexamethasone from full-length human mineralocorticoid receptor expressed in baculovirus infected insect cells after 60...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235970
PNG
(CHEMBL4094464)
Show SMILES COC(=O)c1c(C)nc(C)c(C(=O)CC2CCC2)c1-c1cccc2c1oc(C)cc2=O |(52.63,-36.51,;51.3,-37.29,;49.96,-36.52,;49.96,-34.98,;48.63,-37.3,;48.64,-38.85,;49.97,-39.62,;47.3,-39.62,;45.96,-38.85,;44.63,-39.62,;45.97,-37.3,;44.63,-36.53,;45.39,-35.2,;43.3,-37.3,;43.3,-38.84,;42.21,-39.93,;43.3,-41.02,;44.38,-39.93,;47.29,-36.53,;47.29,-34.99,;48.62,-34.22,;48.62,-32.69,;47.28,-31.92,;45.94,-32.71,;45.95,-34.24,;44.64,-35.01,;43.31,-34.26,;41.99,-35.05,;43.3,-32.73,;44.62,-31.95,;44.61,-30.41,)|
Show InChI InChI=1S/C25H25NO5/c1-13-11-19(27)17-9-6-10-18(24(17)31-13)23-21(20(28)12-16-7-5-8-16)14(2)26-15(3)22(23)25(29)30-4/h6,9-11,16H,5,7-8,12H2,1-4H3
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n/an/a 18n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (734 to 985 residues) expressed in CHO-K1 cells after 5 to 6 hrs by luciferase reporter gene assay


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50398064
PNG
(CHEMBL2181927)
Show SMILES CCOc1ncc(C)c2N=C(C)C([C@@H](c3ccc(cc3OC)C#N)c12)C(N)=O |r,t:9|
Show InChI InChI=1S/C21H22N4O3/c1-5-28-21-18-17(14-7-6-13(9-22)8-15(14)27-4)16(20(23)26)12(3)25-19(18)11(2)10-24-21/h6-8,10,16-17H,5H2,1-4H3,(H2,23,26)/t16?,17-/m1/s1
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n/an/a 18n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (734 to 985 residues) expressed in CHO-K1 cells after 5 to 6 hrs by luciferase reporter gene assay


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50398058
PNG
(CHEMBL2181933 | US8722709, 24)
Show SMILES Cc1ccccc1CCc1ccnc(NC(N)=O)c1
Show InChI InChI=1S/C15H17N3O/c1-11-4-2-3-5-13(11)7-6-12-8-9-17-14(10-12)18-15(16)19/h2-5,8-10H,6-7H2,1H3,(H3,16,17,18,19)
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n/an/a 19n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD expressed in HEK293T cells assessed as inhibition of aldosterone-induced transactivation activity afte...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235969
PNG
(CHEMBL4066981)
Show SMILES CC(C)OC(=O)C1=C(C)NC(C)=C(C1c1cccc2c1oc(C)cc2=O)C(=O)C(F)(F)F |c:6,11|
Show InChI InChI=1S/C23H22F3NO5/c1-10(2)31-22(30)18-13(5)27-12(4)17(21(29)23(24,25)26)19(18)15-8-6-7-14-16(28)9-11(3)32-20(14)15/h6-10,19,27H,1-5H3
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n/an/a 19n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Inhibition of rat brain KYN 3-OHase.


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(RAT)
BDBM50398062
PNG
(CHEMBL2181930)
Show SMILES CC1(C)OC(=S)Nc2ccc(NS(=O)(=O)c3cccs3)cc12
Show InChI InChI=1S/C14H14N2O3S3/c1-14(2)10-8-9(5-6-11(10)15-13(20)19-14)16-22(17,18)12-4-3-7-21-12/h3-8,16H,1-2H3,(H,15,20)
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n/an/a 21n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-Aldosterone from MR in rat kidney cytosolic fraction measured after 18 hrs by liquid scintillation counting method


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235936
PNG
(CHEMBL4099276)
Show SMILES C[C@H](CN1CCOCC1)n1c2ccc(\C=C3/c4ccccc4COc4cc(F)ccc34)cc2[nH]c1=NC#N |r|
Show InChI InChI=1S/C30H28FN5O2/c1-20(17-35-10-12-37-13-11-35)36-28-9-6-21(15-27(28)34-30(36)33-19-32)14-26-24-5-3-2-4-22(24)18-38-29-16-23(31)7-8-25(26)29/h2-9,14-16,20H,10-13,17-18H2,1H3,(H,33,34)/b26-14+/t20-/m1/s1
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n/an/a 21n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at human MR overexpressed in HEK293 cells assessed as inhibition of aldosterone-induced response measured after overnight incubat...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(RAT)
BDBM50235950
PNG
(CHEMBL4087750)
Show SMILES COc1cc(NC(=O)c2ccc(c(CCN(C)C3CC3)c2)-c2ccccc2OC(F)(F)F)ccc1S(N)(=O)=O
Show InChI InChI=1S/C27H28F3N3O5S/c1-33(20-9-10-20)14-13-17-15-18(7-11-21(17)22-5-3-4-6-23(22)38-27(28,29)30)26(34)32-19-8-12-25(39(31,35)36)24(16-19)37-2/h3-8,11-12,15-16,20H,9-10,13-14H2,1-2H3,(H,32,34)(H2,31,35,36)
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n/an/a 22n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-Aldosterone from MR in rat renal soluble fraction measured after 18 hrs in presence of glucocorticoid receptor antagonist RU-486...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235943
PNG
(CHEMBL4099077)
Show SMILES CC(C)OC(=O)C1=C(C)NC(C)=C(C#N)C1c1cccc2C(=O)c3ccccc3-c12 |c:6,t:11|
Show InChI InChI=1S/C25H22N2O3/c1-13(2)30-25(29)21-15(4)27-14(3)20(12-26)23(21)18-10-7-11-19-22(18)16-8-5-6-9-17(16)24(19)28/h5-11,13,23,27H,1-4H3
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n/an/a 23n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (734 to 985 residues) expressed in CHO-K1 cells after 5 to 6 hrs by luciferase reporter gene assay


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235963
PNG
(CHEMBL4097160)
Show SMILES C[C@@H]1CN([C@@H](CO1)c1ccccc1)c1ccc2OCC(=O)Nc2c1 |r|
Show InChI InChI=1S/C19H20N2O3/c1-13-10-21(17(11-23-13)14-5-3-2-4-6-14)15-7-8-18-16(9-15)20-19(22)12-24-18/h2-9,13,17H,10-12H2,1H3,(H,20,22)/t13-,17+/m1/s1
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n/an/a 24n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused MR LBD (unknown origin) expressed in human Huh7 cells assessed as inhibition of aldosterone-induced transcriptional...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235957
PNG
(CHEMBL4075462)
Show SMILES COc1ccccc1CCc1cccc(NC(N)=O)n1
Show InChI InChI=1S/C15H17N3O2/c1-20-13-7-3-2-5-11(13)9-10-12-6-4-8-14(17-12)18-15(16)19/h2-8H,9-10H2,1H3,(H3,16,17,18,19)
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n/an/a 25n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of TAMRA-labeled dexamethasone from full-length human mineralocorticoid receptor expressed in baculovirus infected insect cells after 60...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235973
PNG
(CHEMBL4096901)
Show SMILES CCOc1ncc(C)c2NC(C)=C(C#N)[C@@H](c3ccc(cc3OC)C#N)c12 |r,t:11|
Show InChI InChI=1S/C21H20N4O2/c1-5-27-21-19-18(15-7-6-14(9-22)8-17(15)26-4)16(10-23)13(3)25-20(19)12(2)11-24-21/h6-8,11,18,25H,5H2,1-4H3/t18-/m1/s1
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n/an/a 26n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (734 to 985 residues) expressed in CHO-K1 cells after 5 to 6 hrs by luciferase reporter gene assay


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50398063
PNG
(CHEMBL2181926)
Show SMILES CCOC(=O)C1=C(C)N=C(C)C([C@H]1c1cccc2c1oc(C)cc2=O)C(C)=O |r,c:5,t:8|
Show InChI InChI=1S/C22H23NO5/c1-6-27-22(26)19-13(4)23-12(3)18(14(5)24)20(19)16-9-7-8-15-17(25)10-11(2)28-21(15)16/h7-10,18,20H,6H2,1-5H3/t18?,20-/m1/s1
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n/an/a 28n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Inhibition of rat liver KYN 3-OHase.


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM121444
PNG
(US8722709, 48)
Show SMILES Cc1cc(F)ccc1CCc1ccnc(NC(N)=O)c1
Show InChI InChI=1S/C15H16FN3O/c1-10-8-13(16)5-4-12(10)3-2-11-6-7-18-14(9-11)19-15(17)20/h4-9H,2-3H2,1H3,(H3,17,18,19,20)
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n/an/a 31n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD expressed in HEK293T cells assessed as inhibition of aldosterone-induced transactivation activity afte...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(RAT)
BDBM50235982
PNG
(CHEMBL4085281)
Show SMILES COc1cc(NC(=O)c2ccc(c(COC(C)=O)c2)-c2ccccc2C(F)(F)F)ccc1S(N)(=O)=O
Show InChI InChI=1S/C24H21F3N2O6S/c1-14(30)35-13-16-11-15(7-9-18(16)19-5-3-4-6-20(19)24(25,26)27)23(31)29-17-8-10-22(36(28,32)33)21(12-17)34-2/h3-12H,13H2,1-2H3,(H,29,31)(H2,28,32,33)
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n/an/a 31n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Displacement of [3H]-Aldosterone from MR in rat renal soluble fraction measured after 18 hrs in presence of glucocorticoid receptor antagonist RU-486...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235966
PNG
(CHEMBL4091401)
Show SMILES C[C@@H]1CN([C@@H](CO1)c1ccccc1F)c1ccc2OCC(=O)Nc2c1 |r|
Show InChI InChI=1S/C19H19FN2O3/c1-12-9-22(17(10-24-12)14-4-2-3-5-15(14)20)13-6-7-18-16(8-13)21-19(23)11-25-18/h2-8,12,17H,9-11H2,1H3,(H,21,23)/t12-,17+/m1/s1
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n/an/a 33n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Inhibition of rat liver KYN 3-OHase.


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235939
PNG
(CHEMBL4102462)
Show SMILES CC(C)OC(=O)C1=C(C)NC(C)=C(C1c1cccc2c1oc(C)cc2=O)C(C)=O |c:6,11|
Show InChI InChI=1S/C23H25NO5/c1-11(2)28-23(27)20-14(5)24-13(4)19(15(6)25)21(20)17-9-7-8-16-18(26)10-12(3)29-22(16)17/h7-11,21,24H,1-6H3
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n/an/a 39n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (734 to 985 residues) expressed in CHO-K1 cells after 5 to 6 hrs by luciferase reporter gene assay


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM121428
PNG
(US8722709, 32)
Show SMILES CC(Cc1ccnc(NC(N)=O)c1)c1ccccc1C
Show InChI InChI=1S/C16H19N3O/c1-11-5-3-4-6-14(11)12(2)9-13-7-8-18-15(10-13)19-16(17)20/h3-8,10,12H,9H2,1-2H3,(H3,17,18,19,20)
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n/an/a 43n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD expressed in HEK293T cells assessed as inhibition of aldosterone-induced transactivation activity afte...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM121427
PNG
(US8722709, 31)
Show SMILES NC(=O)Nc1cc(CC(c2ccccc2)c2ccccc2)ccn1
Show InChI InChI=1S/C20H19N3O/c21-20(24)23-19-14-15(11-12-22-19)13-18(16-7-3-1-4-8-16)17-9-5-2-6-10-17/h1-12,14,18H,13H2,(H3,21,22,23,24)
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n/an/a 44n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD expressed in HEK293T cells assessed as inhibition of aldosterone-induced transactivation activity afte...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50398061
PNG
(CHEMBL2181928)
Show SMILES C[C@@H]1CN([C@@H](CO1)c1ccccc1)c1ccc2OCC(=O)Nc2n1 |r|
Show InChI InChI=1S/C18H19N3O3/c1-12-9-21(14(10-23-12)13-5-3-2-4-6-13)16-8-7-15-18(19-16)20-17(22)11-24-15/h2-8,12,14H,9-11H2,1H3,(H,19,20,22)/t12-,14+/m1/s1
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n/an/a 44n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused MR LBD (unknown origin) expressed in human Huh7 cells assessed as inhibition of aldosterone-induced transcriptional...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235972
PNG
(CHEMBL4068008)
Show SMILES CCOc1nccc2NC(C)=C(C#N)[C@@H](c3ccc(cc3OC)C#N)c12 |r,t:10|
Show InChI InChI=1S/C20H18N4O2/c1-4-26-20-19-16(7-8-23-20)24-12(2)15(11-22)18(19)14-6-5-13(10-21)9-17(14)25-3/h5-9,18,24H,4H2,1-3H3/t18-/m1/s1
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n/an/a 47n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (734 to 985 residues) expressed in CHO-K1 cells after 5 to 6 hrs by luciferase reporter gene assay


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235962
PNG
(CHEMBL4067551)
Show SMILES Cc1cccc(c1)-c1ccc2OCC(=O)Nc2c1C
Show InChI InChI=1S/C16H15NO2/c1-10-4-3-5-12(8-10)13-6-7-14-16(11(13)2)17-15(18)9-19-14/h3-8H,9H2,1-2H3,(H,17,18)
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n/an/a 47n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused human MR LBD (672 to 984 residues) expressed in HEK293T cells assessed as inhibition of aldosterone-induced transac...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235968
PNG
(CHEMBL4069468)
Show SMILES C[C@@H]1CN([C@@H](CO1)c1ccccc1F)c1cc2NC(=O)COc2cn1 |r|
Show InChI InChI=1S/C18H18FN3O3/c1-11-8-22(15(9-24-11)12-4-2-3-5-13(12)19)17-6-14-16(7-20-17)25-10-18(23)21-14/h2-7,11,15H,8-10H2,1H3,(H,21,23)/t11-,15+/m1/s1
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n/an/a 54n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused MR LBD (unknown origin) expressed in human Huh7 cells assessed as inhibition of aldosterone-induced transcriptional...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50235967
PNG
(CHEMBL4063566)
Show SMILES C[C@@H]1CN([C@@H](CO1)c1cccc(F)c1)c1ccc2OCC(=O)Nc2c1 |r|
Show InChI InChI=1S/C19H19FN2O3/c1-12-9-22(17(10-24-12)13-3-2-4-14(20)7-13)15-5-6-18-16(8-15)21-19(23)11-25-18/h2-8,12,17H,9-11H2,1H3,(H,21,23)/t12-,17+/m1/s1
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n/an/a 55n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Antagonist activity at Gal4-fused MR LBD (unknown origin) expressed in human Huh7 cells assessed as inhibition of aldosterone-induced transcriptional...


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
Mineralocorticoid receptor


(Homo sapiens (Human))
BDBM50398064
PNG
(CHEMBL2181927)
Show SMILES CCOc1ncc(C)c2N=C(C)C([C@@H](c3ccc(cc3OC)C#N)c12)C(N)=O |r,t:9|
Show InChI InChI=1S/C21H22N4O3/c1-5-28-21-18-17(14-7-6-13(9-22)8-15(14)27-4)16(20(23)26)12(3)25-19(18)11(2)10-24-21/h6-8,10,16-17H,5H2,1-4H3,(H2,23,26)/t16?,17-/m1/s1
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n/an/a 58n/an/an/an/an/an/a



Instituto de Qu£mica M£dica (IQM-CSIC)

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibition of rat brain KYN 3-OHase


J Med Chem 60: 2629-2650 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01065
BindingDB Entry DOI: 10.7270/Q2HD7XXB
More data for this
Ligand-Target Pair
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