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Compile Data Set for Download or QSAR

Found 21 hits with Last Name = 'cato' and Initial = 'ml'   
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
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605641
PNG
(CHEMBL5177743)
Show SMILES NS(=O)(=O)N[C@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:24|
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0.150n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50511467
PNG
(CHEMBL4551205)
Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CC[C@H](NS(N)(=O)=O)C2C1)C(=C)c1ccccc1 |r,c:6|
Show InChI InChI=1S/C28H36N2O2S/c1-3-4-5-8-17-24-20-25-26(30-33(29,31)32)18-19-28(25,21(2)22-13-9-6-10-14-22)27(24)23-15-11-7-12-16-23/h6-7,9-16,25-26,30H,2-5,8,17-20H2,1H3,(H2,29,31,32)/t25?,26-,28-/m0/s1
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1.30n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605640
PNG
(CHEMBL5198453)
Show SMILES O[C@@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:20|
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5.30n/an/an/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50544056
PNG
(CHEMBL4644327)
Show SMILES [H][C@@]12CC(CCCCCCCCCC(O)=O)=C(c3ccccc3)[C@]1(CN(C)c1ccccc1)CC[C@H]2O |r,t:15|
Show InChI InChI=1S/C32H43NO3/c1-33(27-18-12-8-13-19-27)24-32-22-21-29(34)28(32)23-26(31(32)25-15-10-7-11-16-25)17-9-5-3-2-4-6-14-20-30(35)36/h7-8,10-13,15-16,18-19,28-29,34H,2-6,9,14,17,20-24H2,1H3,(H,35,36)/t28-,29+,32-/m0/s1
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18n/an/an/an/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127293
BindingDB Entry DOI: 10.7270/Q2GH9NH4
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50544057
PNG
(CHEMBL4637563)
Show SMILES [H][C@@]12CC(CCCCCC)=C(c3ccccc3)[C@]1(CN(C)c1ccccc1)CC[C@@H]2NS(N)(=O)=O |r,t:9|
Show InChI InChI=1S/C28H39N3O2S/c1-3-4-5-8-15-23-20-25-26(30-34(29,32)33)18-19-28(25,27(23)22-13-9-6-10-14-22)21-31(2)24-16-11-7-12-17-24/h6-7,9-14,16-17,25-26,30H,3-5,8,15,18-21H2,1-2H3,(H2,29,32,33)/t25-,26-,28-/m0/s1
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38n/an/an/an/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127293
BindingDB Entry DOI: 10.7270/Q2GH9NH4
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50544055
PNG
(CHEMBL4645796)
Show SMILES [H][C@@]12CC(CCCCCC)=C(c3ccccc3)[C@]1([H])CC[C@@H]2NS(N)(=O)=O |r,t:9|
Show InChI InChI=1S/C20H30N2O2S/c1-2-3-4-6-11-16-14-18-17(12-13-19(18)22-25(21,23)24)20(16)15-9-7-5-8-10-15/h5,7-10,17-19,22H,2-4,6,11-14H2,1H3,(H2,21,23,24)/t17-,18-,19+/m1/s1
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56n/an/an/an/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127293
BindingDB Entry DOI: 10.7270/Q2GH9NH4
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50544054
PNG
(CHEMBL4638625)
Show SMILES [H][C@@]12CC(CCCCCCCCCC(O)=O)=C(c3ccccc3)[C@]1([H])CC[C@H]2O |r,t:15|
Show InChI InChI=1S/C24H34O3/c25-22-16-15-20-21(22)17-19(24(20)18-11-8-6-9-12-18)13-7-4-2-1-3-5-10-14-23(26)27/h6,8-9,11-12,20-22,25H,1-5,7,10,13-17H2,(H,26,27)/t20-,21-,22-/m1/s1
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280n/an/an/an/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Displacement of 6N-FAM from human LRH1 LBD (299 to 541 residues) expressed in Escherichia coli BL21 pLysS by competitive binding based fluorescence p...


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127293
BindingDB Entry DOI: 10.7270/Q2GH9NH4
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605641
PNG
(CHEMBL5177743)
Show SMILES NS(=O)(=O)N[C@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:24|
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n/an/an/a 1.80E+3n/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50511467
PNG
(CHEMBL4551205)
Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CC[C@H](NS(N)(=O)=O)C2C1)C(=C)c1ccccc1 |r,c:6|
Show InChI InChI=1S/C28H36N2O2S/c1-3-4-5-8-17-24-20-25-26(30-33(29,31)32)18-19-28(25,21(2)22-13-9-6-10-14-22)27(24)23-15-11-7-12-16-23/h6-7,9-16,25-26,30H,2-5,8,17-20H2,1H3,(H2,29,31,32)/t25?,26-,28-/m0/s1
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TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605640
PNG
(CHEMBL5198453)
Show SMILES O[C@@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:20|
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TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605641
PNG
(CHEMBL5177743)
Show SMILES NS(=O)(=O)N[C@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:24|
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n/an/an/a 120n/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50511467
PNG
(CHEMBL4551205)
Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CC[C@H](NS(N)(=O)=O)C2C1)C(=C)c1ccccc1 |r,c:6|
Show InChI InChI=1S/C28H36N2O2S/c1-3-4-5-8-17-24-20-25-26(30-33(29,31)32)18-19-28(25,21(2)22-13-9-6-10-14-22)27(24)23-15-11-7-12-16-23/h6-7,9-16,25-26,30H,2-5,8,17-20H2,1H3,(H2,29,31,32)/t25?,26-,28-/m0/s1
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TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605640
PNG
(CHEMBL5198453)
Show SMILES O[C@@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:20|
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TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605640
PNG
(CHEMBL5198453)
Show SMILES O[C@@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:20|
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n/an/an/a 2.50E+3n/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50511467
PNG
(CHEMBL4551205)
Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CC[C@H](NS(N)(=O)=O)C2C1)C(=C)c1ccccc1 |r,c:6|
Show InChI InChI=1S/C28H36N2O2S/c1-3-4-5-8-17-24-20-25-26(30-33(29,31)32)18-19-28(25,21(2)22-13-9-6-10-14-22)27(24)23-15-11-7-12-16-23/h6-7,9-16,25-26,30H,2-5,8,17-20H2,1H3,(H2,29,31,32)/t25?,26-,28-/m0/s1
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n/an/an/a 2.10E+3n/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605641
PNG
(CHEMBL5177743)
Show SMILES NS(=O)(=O)N[C@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:24|
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n/an/an/an/a 43n/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605641
PNG
(CHEMBL5177743)
Show SMILES NS(=O)(=O)N[C@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:24|
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n/an/an/a 340n/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50511467
PNG
(CHEMBL4551205)
Show SMILES CCCCCCC1=C(c2ccccc2)[C@@]2(CC[C@H](NS(N)(=O)=O)C2C1)C(=C)c1ccccc1 |r,c:6|
Show InChI InChI=1S/C28H36N2O2S/c1-3-4-5-8-17-24-20-25-26(30-33(29,31)32)18-19-28(25,21(2)22-13-9-6-10-14-22)27(24)23-15-11-7-12-16-23/h6-7,9-16,25-26,30H,2-5,8,17-20H2,1H3,(H2,29,31,32)/t25?,26-,28-/m0/s1
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TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50544057
PNG
(CHEMBL4637563)
Show SMILES [H][C@@]12CC(CCCCCC)=C(c3ccccc3)[C@]1(CN(C)c1ccccc1)CC[C@@H]2NS(N)(=O)=O |r,t:9|
Show InChI InChI=1S/C28H39N3O2S/c1-3-4-5-8-15-23-20-25-26(30-34(29,32)33)18-19-28(25,27(23)22-13-9-6-10-14-22)21-31(2)24-16-11-7-12-17-24/h6-7,9-14,16-17,25-26,30H,3-5,8,15,18-21H2,1-2H3,(H2,29,32,33)/t25-,26-,28-/m0/s1
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n/an/an/an/a 400n/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Agonist activity at LRH1 (unknown origin) by luciferase reporter gene assay


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127293
BindingDB Entry DOI: 10.7270/Q2GH9NH4
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50544056
PNG
(CHEMBL4644327)
Show SMILES [H][C@@]12CC(CCCCCCCCCC(O)=O)=C(c3ccccc3)[C@]1(CN(C)c1ccccc1)CC[C@H]2O |r,t:15|
Show InChI InChI=1S/C32H43NO3/c1-33(27-18-12-8-13-19-27)24-32-22-21-29(34)28(32)23-26(31(32)25-15-10-7-11-16-25)17-9-5-3-2-4-6-14-20-30(35)36/h7-8,10-13,15-16,18-19,28-29,34H,2-6,9,14,17,20-24H2,1H3,(H,35,36)/t28-,29+,32-/m0/s1
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n/an/an/an/a 2.40E+3n/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Agonist activity at LRH1 (unknown origin) by luciferase reporter gene assay


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2020.127293
BindingDB Entry DOI: 10.7270/Q2GH9NH4
More data for this
Ligand-Target Pair
Nuclear receptor subfamily 5 group A member 2


(Homo sapiens (Human))
BDBM50605640
PNG
(CHEMBL5198453)
Show SMILES O[C@@H]1CC[C@@]2(C1CC(CCCCCCCCCC(O)=O)=C2c1ccccc1)C(=C)c1ccccc1 |r,c:20|
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n/an/an/an/a 1.70E+3n/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1021/acs.jmedchem.2c00235
BindingDB Entry DOI: 10.7270/Q23J3J2Q
More data for this
Ligand-Target Pair