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27 similar compounds to monomer 50077094

Compile data set for download or QSAR
Wt: 296.2
BDBM18190
Wt: 324.3
BDBM50063096
Wt: 324.3
BDBM50063101
Wt: 310.3
BDBM50063108
Wt: 324.3
BDBM50063109
Wt: 338.3
BDBM50063110
Wt: 310.3
BDBM50063111
Wt: 324.3
BDBM50063113
Wt: 338.3
BDBM50063116
Wt: 336.3
BDBM50063118
Wt: 296.2
BDBM50077099
Wt: 324.3
BDBM50077100
Wt: 324.2
BDBM50077101
Wt: 310.3
BDBM50077105
Wt: 310.3
BDBM50077107
Displayed 1 to 15 (of 27 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 50 hits for monomerid = 18190,50063096,50063101,50063108,50063109,50063110,50063111,50063113,50063116,50063118,50077099,50077100,50077101,50077105,50077107   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Androgen Receptor


(Homo sapiens (Human))
BDBM18190
PNG
(6-ethyl-4-(trifluoromethyl)-1H,2H,6H,7H,8H,9H-pyri...)
Show SMILES CCC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-2-8-3-4-19-12-7-13-10(5-9(8)12)11(15(16,17)18)6-14(21)20-13/h5-8,19H,2-4H2,1H3,(H,20,21)
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7n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity to the human androgen receptor (hAR), using [3H]DHT as radioligand in a competitive binding assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077105
PNG
(CHEMBL418198 | Trans-6-Ethyl-7-methyl-4-trifluorom...)
Show SMILES CCC1[C@@H](C)CNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-3-9-8(2)7-20-13-6-14-11(4-10(9)13)12(16(17,18)19)5-15(22)21-14/h4-6,8-9,20H,3,7H2,1-2H3,(H,21,22)/t8-,9?/m0/s1
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8n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity to the human androgen receptor (hAR), using [3H]DHT as radioligand in a competitive binding assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063110
PNG
(8-Ethyl-1,8,9-trimethyl-4-trifluoromethyl-6,7,8,9-...)
Show SMILES CCC1(C)CCc2cc3c(cc(=O)n(C)c3cc2N1C)C(F)(F)F
Show InChI InChI=1S/C18H21F3N2O/c1-5-17(2)7-6-11-8-12-13(18(19,20)21)9-16(24)22(3)15(12)10-14(11)23(17)4/h8-10H,5-7H2,1-4H3
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10n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM18190
PNG
(6-ethyl-4-(trifluoromethyl)-1H,2H,6H,7H,8H,9H-pyri...)
Show SMILES CCC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-2-8-3-4-19-12-7-13-10(5-9(8)12)11(15(16,17)18)6-14(21)20-13/h5-8,19H,2-4H2,1H3,(H,20,21)
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11 -11.3n/an/a 4.10n/an/a7.437



Ligand Pharmaceuticals Inc.



Assay Description
The compounds were evaluated in a transcriptional activation assay with hAR in a mammalian cell background (CV-1) as the primary in vitro assay. Rece...


J Med Chem 50: 2486-96 (2007)


Article DOI: 10.1021/jm061329j
BindingDB Entry DOI: 10.7270/Q20R9MNK
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077099
PNG
(CHEMBL436344 | Trans-6,7-Dimethyl-4-trifluoromethy...)
Show SMILES C[C@H]1CNc2cc3[nH]c(=O)cc(c3cc2C1C)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-7-6-19-12-5-13-10(3-9(12)8(7)2)11(15(16,17)18)4-14(21)20-13/h3-5,7-8,19H,6H2,1-2H3,(H,20,21)/t7-,8?/m0/s1
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16n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity to the human androgen receptor (hAR), using [3H]DHT as radioligand in a competitive binding assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM18190
PNG
(6-ethyl-4-(trifluoromethyl)-1H,2H,6H,7H,8H,9H-pyri...)
Show SMILES CCC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-2-8-3-4-19-12-7-13-10(5-9(8)12)11(15(16,17)18)6-14(21)20-13/h5-8,19H,2-4H2,1H3,(H,20,21)
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17n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human Androgen receptor expressed in COS-1 cells


J Med Chem 42: 210-2 (1999)


Article DOI: 10.1021/jm9806648
BindingDB Entry DOI: 10.7270/Q2F76D8W
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063096
PNG
(1,8,8,9-Tetramethyl-4-trifluoromethyl-6,7,8,9-tetr...)
Show SMILES CN1c2cc3n(C)c(=O)cc(c3cc2CCC1(C)C)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-16(2)6-5-10-7-11-12(17(18,19)20)8-15(23)21(3)14(11)9-13(10)22(16)4/h7-9H,5-6H2,1-4H3
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17n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077100
PNG
(6-Isobutyl-4-trifluoromethyl-6,7,8,9-tetrahydro-1H...)
Show SMILES CC(C)CC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-9(2)5-10-3-4-21-14-8-15-12(6-11(10)14)13(17(18,19)20)7-16(23)22-15/h6-10,21H,3-5H2,1-2H3,(H,22,23)
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22n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity to the human androgen receptor (hAR), using [3H]DHT as radioligand in a competitive binding assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063116
PNG
(1,6,8,8,10-Pentamethyl-4-trifluoromethyl-6,7,8,9-t...)
Show SMILES CC1CC(C)(C)Nc2c(C)c3n(C)c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C18H21F3N2O/c1-9-8-17(3,4)22-15-10(2)16-12(6-11(9)15)13(18(19,20)21)7-14(24)23(16)5/h6-7,9,22H,8H2,1-5H3
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40n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063113
PNG
(1,6,8,8-Tetramethyl-4-trifluoromethyl-6,7,8,9-tetr...)
Show SMILES CC1CC(C)(C)Nc2cc3n(C)c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-9-8-16(2,3)21-13-7-14-11(5-10(9)13)12(17(18,19)20)6-15(23)22(14)4/h5-7,9,21H,8H2,1-4H3
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46n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063109
PNG
(6-Ethyl-8,8-dimethyl-4-trifluoromethyl-6,7,8,9-tet...)
Show SMILES CCC1CC(C)(C)Nc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-4-9-8-16(2,3)22-14-7-13-11(5-10(9)14)12(17(18,19)20)6-15(23)21-13/h5-7,9,22H,4,8H2,1-3H3,(H,21,23)
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54n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063111
PNG
(1,8,8-Trimethyl-4-trifluoromethyl-6,7,8,9-tetrahyd...)
Show SMILES Cn1c2cc3NC(C)(C)CCc3cc2c(cc1=O)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-15(2)5-4-9-6-10-11(16(17,18)19)7-14(22)21(3)13(10)8-12(9)20-15/h6-8,20H,4-5H2,1-3H3
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56n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063101
PNG
(8-Ethyl-1,8-dimethyl-4-trifluoromethyl-6,7,8,9-tet...)
Show SMILES CCC1(C)CCc2cc3c(cc(=O)n(C)c3cc2N1)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-4-16(2)6-5-10-7-11-12(17(18,19)20)8-15(23)22(3)14(11)9-13(10)21-16/h7-9,21H,4-6H2,1-3H3
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69n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063108
PNG
(6,8,8-Trimethyl-4-trifluoromethyl-6,7,8,9-tetrahyd...)
Show SMILES CC1CC(C)(C)Nc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-8-7-15(2,3)21-13-6-12-10(4-9(8)13)11(16(17,18)19)5-14(22)20-12/h4-6,8,21H,7H2,1-3H3,(H,20,22)
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76n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063118
PNG
(3a,10-Dimethyl-7-trifluoromethyl-1,2,3a,4,5,10-hex...)
Show SMILES Cn1c2cc3N4CCCC4(C)CCc3cc2c(cc1=O)C(F)(F)F
Show InChI InChI=1S/C18H19F3N2O/c1-17-5-3-7-23(17)14-10-15-12(8-11(14)4-6-17)13(18(19,20)21)9-16(24)22(15)2/h8-10H,3-7H2,1-2H3
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78n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity for human androgen receptor in transiently-transfected COS-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077107
PNG
(6-Ethyl-9-methyl-4-trifluoromethyl-6,7,8,9-tetrahy...)
Show SMILES CCC1CCN(C)c2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-3-9-4-5-21(2)14-8-13-11(6-10(9)14)12(16(17,18)19)7-15(22)20-13/h6-9H,3-5H2,1-2H3,(H,20,22)
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630n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity to the human androgen receptor (hAR), using [3H]DHT as radioligand in a competitive binding assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077101
PNG
(4-Ethyl-8-oxo-6-trifluoromethyl-3,4,8,9-tetrahydro...)
Show SMILES CCC1CCN(C=O)c2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H15F3N2O2/c1-2-9-3-4-21(8-22)14-7-13-11(5-10(9)14)12(16(17,18)19)6-15(23)20-13/h5-9H,2-4H2,1H3,(H,20,23)
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>1.00E+3n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Agonist activity to the human androgen receptor (hAR) in CV-1 cells


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063109
PNG
(6-Ethyl-8,8-dimethyl-4-trifluoromethyl-6,7,8,9-tet...)
Show SMILES CCC1CC(C)(C)Nc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-4-9-8-16(2,3)22-14-7-13-11(5-10(9)14)12(17(18,19)20)6-15(23)21-13/h5-7,9,22H,4,8H2,1-3H3,(H,21,23)
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n/an/a 274n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063118
PNG
(3a,10-Dimethyl-7-trifluoromethyl-1,2,3a,4,5,10-hex...)
Show SMILES Cn1c2cc3N4CCCC4(C)CCc3cc2c(cc1=O)C(F)(F)F
Show InChI InChI=1S/C18H19F3N2O/c1-17-5-3-7-23(17)14-10-15-12(8-11(14)4-6-17)13(18(19,20)21)9-16(24)22(15)2/h8-10H,3-7H2,1-2H3
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n/an/a 398n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063113
PNG
(1,6,8,8-Tetramethyl-4-trifluoromethyl-6,7,8,9-tetr...)
Show SMILES CC1CC(C)(C)Nc2cc3n(C)c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-9-8-16(2,3)21-13-7-14-11(5-10(9)13)12(17(18,19)20)6-15(23)22(14)4/h5-7,9,21H,8H2,1-4H3
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n/an/a 585n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063111
PNG
(1,8,8-Trimethyl-4-trifluoromethyl-6,7,8,9-tetrahyd...)
Show SMILES Cn1c2cc3NC(C)(C)CCc3cc2c(cc1=O)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-15(2)5-4-9-6-10-11(16(17,18)19)7-14(22)21(3)13(10)8-12(9)20-15/h6-8,20H,4-5H2,1-3H3
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n/an/a 1.24E+3n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063101
PNG
(8-Ethyl-1,8-dimethyl-4-trifluoromethyl-6,7,8,9-tet...)
Show SMILES CCC1(C)CCc2cc3c(cc(=O)n(C)c3cc2N1)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-4-16(2)6-5-10-7-11-12(17(18,19)20)8-15(23)22(3)14(11)9-13(10)21-16/h7-9,21H,4-6H2,1-3H3
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n/an/a 48n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063096
PNG
(1,8,8,9-Tetramethyl-4-trifluoromethyl-6,7,8,9-tetr...)
Show SMILES CN1c2cc3n(C)c(=O)cc(c3cc2CCC1(C)C)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-16(2)6-5-10-7-11-12(17(18,19)20)8-15(23)21(3)14(11)9-13(10)22(16)4/h7-9H,5-6H2,1-4H3
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n/an/a 2.20E+3n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063096
PNG
(1,8,8,9-Tetramethyl-4-trifluoromethyl-6,7,8,9-tetr...)
Show SMILES CN1c2cc3n(C)c(=O)cc(c3cc2CCC1(C)C)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-16(2)6-5-10-7-11-12(17(18,19)20)8-15(23)21(3)14(11)9-13(10)22(16)4/h7-9H,5-6H2,1-4H3
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n/an/a 19n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM18190
PNG
(6-ethyl-4-(trifluoromethyl)-1H,2H,6H,7H,8H,9H-pyri...)
Show SMILES CCC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-2-8-3-4-19-12-7-13-10(5-9(8)12)11(15(16,17)18)6-14(21)20-13/h5-8,19H,2-4H2,1H3,(H,20,21)
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n/an/a 4.58E+3n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Agonist activity to the human androgen receptor (hAR) in CV-1 cells


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM18190
PNG
(6-ethyl-4-(trifluoromethyl)-1H,2H,6H,7H,8H,9H-pyri...)
Show SMILES CCC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-2-8-3-4-19-12-7-13-10(5-9(8)12)11(15(16,17)18)6-14(21)20-13/h5-8,19H,2-4H2,1H3,(H,20,21)
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n/an/an/an/a 4n/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity to the human androgen receptor (hAR), using [3H]DHT as radioligand in a competitive binding assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077100
PNG
(6-Isobutyl-4-trifluoromethyl-6,7,8,9-tetrahydro-1H...)
Show SMILES CC(C)CC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-9(2)5-10-3-4-21-14-8-15-12(6-11(10)14)13(17(18,19)20)7-16(23)22-15/h6-10,21H,3-5H2,1-2H3,(H,22,23)
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n/an/an/an/a 25n/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Agonist activity to the human androgen receptor (hAR) in CV-1 cells


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077105
PNG
(CHEMBL418198 | Trans-6-Ethyl-7-methyl-4-trifluorom...)
Show SMILES CCC1[C@@H](C)CNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-3-9-8(2)7-20-13-6-14-11(4-10(9)13)12(16(17,18)19)5-15(22)21-14/h4-6,8-9,20H,3,7H2,1-2H3,(H,21,22)/t8-,9?/m0/s1
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n/an/an/an/a 7n/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity to the human androgen receptor (hAR), using [3H]DHT as radioligand in a competitive binding assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077107
PNG
(6-Ethyl-9-methyl-4-trifluoromethyl-6,7,8,9-tetrahy...)
Show SMILES CCC1CCN(C)c2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-3-9-4-5-21(2)14-8-13-11(6-10(9)14)12(16(17,18)19)7-15(22)20-13/h6-9H,3-5H2,1-2H3,(H,20,22)
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n/an/a>1.00E+4n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Binding affinity to the human androgen receptor (hAR), using [3H]DHT as radioligand in a competitive binding assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077101
PNG
(4-Ethyl-8-oxo-6-trifluoromethyl-3,4,8,9-tetrahydro...)
Show SMILES CCC1CCN(C=O)c2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H15F3N2O2/c1-2-9-3-4-21(8-22)14-7-13-11(5-10(9)14)12(16(17,18)19)6-15(23)20-13/h5-9H,2-4H2,1H3,(H,20,23)
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n/an/a>1.00E+4n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Agonist activity to the human androgen receptor (hAR) in CV-1 cells


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077099
PNG
(CHEMBL436344 | Trans-6,7-Dimethyl-4-trifluoromethy...)
Show SMILES C[C@H]1CNc2cc3[nH]c(=O)cc(c3cc2C1C)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-7-6-19-12-5-13-10(3-9(12)8(7)2)11(15(16,17)18)4-14(21)20-13/h3-5,7-8,19H,6H2,1-2H3,(H,20,21)/t7-,8?/m0/s1
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n/an/an/an/a 10n/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Agonist activity to the human androgen receptor (hAR) in CV-1 cells


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077099
PNG
(CHEMBL436344 | Trans-6,7-Dimethyl-4-trifluoromethy...)
Show SMILES C[C@H]1CNc2cc3[nH]c(=O)cc(c3cc2C1C)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-7-6-19-12-5-13-10(3-9(12)8(7)2)11(15(16,17)18)4-14(21)20-13/h3-5,7-8,19H,6H2,1-2H3,(H,20,21)/t7-,8?/m0/s1
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n/an/a>1.00E+4n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in CV-1 cells was determined as a function of maximal inhibition of dihydrotestosterone u...


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063110
PNG
(8-Ethyl-1,8,9-trimethyl-4-trifluoromethyl-6,7,8,9-...)
Show SMILES CCC1(C)CCc2cc3c(cc(=O)n(C)c3cc2N1C)C(F)(F)F
Show InChI InChI=1S/C18H21F3N2O/c1-5-17(2)7-6-11-8-12-13(18(19,20)21)9-16(24)22(3)15(12)10-14(11)23(17)4/h8-10H,5-7H2,1-4H3
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n/an/a 24n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063101
PNG
(8-Ethyl-1,8-dimethyl-4-trifluoromethyl-6,7,8,9-tet...)
Show SMILES CCC1(C)CCc2cc3c(cc(=O)n(C)c3cc2N1)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-4-16(2)6-5-10-7-11-12(17(18,19)20)8-15(23)22(3)14(11)9-13(10)21-16/h7-9,21H,4-6H2,1-3H3
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n/an/a 3.28E+3n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063110
PNG
(8-Ethyl-1,8,9-trimethyl-4-trifluoromethyl-6,7,8,9-...)
Show SMILES CCC1(C)CCc2cc3c(cc(=O)n(C)c3cc2N1C)C(F)(F)F
Show InChI InChI=1S/C18H21F3N2O/c1-5-17(2)7-6-11-8-12-13(18(19,20)21)9-16(24)22(3)15(12)10-14(11)23(17)4/h8-10H,5-7H2,1-4H3
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n/an/a 1.11E+3n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063108
PNG
(6,8,8-Trimethyl-4-trifluoromethyl-6,7,8,9-tetrahyd...)
Show SMILES CC1CC(C)(C)Nc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-8-7-15(2,3)21-13-6-12-10(4-9(8)13)11(16(17,18)19)5-14(22)20-12/h4-6,8,21H,7H2,1-3H3,(H,20,22)
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n/an/a 231n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077101
PNG
(4-Ethyl-8-oxo-6-trifluoromethyl-3,4,8,9-tetrahydro...)
Show SMILES CCC1CCN(C=O)c2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H15F3N2O2/c1-2-9-3-4-21(8-22)14-7-13-11(5-10(9)14)12(16(17,18)19)6-15(23)20-13/h5-9H,2-4H2,1H3,(H,20,23)
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n/an/an/an/a 137n/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Agonist activity to the human androgen receptor (hAR) in CV-1 cells


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077105
PNG
(CHEMBL418198 | Trans-6-Ethyl-7-methyl-4-trifluorom...)
Show SMILES CCC1[C@@H](C)CNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-3-9-8(2)7-20-13-6-14-11(4-10(9)13)12(16(17,18)19)5-15(22)21-14/h4-6,8-9,20H,3,7H2,1-2H3,(H,21,22)/t8-,9?/m0/s1
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n/an/a 2.71E+3n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in CV-1 cells using cotransfection assay


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM18190
PNG
(6-ethyl-4-(trifluoromethyl)-1H,2H,6H,7H,8H,9H-pyri...)
Show SMILES CCC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-2-8-3-4-19-12-7-13-10(5-9(8)12)11(15(16,17)18)6-14(21)20-13/h5-8,19H,2-4H2,1H3,(H,20,21)
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n/an/an/an/a 3n/an/an/an/a



GTx, Inc.

Curated by ChEMBL


Assay Description
Agonist activity at androgen receptor (unknown origin) assessed as receptor transactivation by reporter gene assay


J Med Chem 52: 3597-617 (2009)


Article DOI: 10.1021/jm900280m
BindingDB Entry DOI: 10.7270/Q2GH9HWD
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM18190
PNG
(6-ethyl-4-(trifluoromethyl)-1H,2H,6H,7H,8H,9H-pyri...)
Show SMILES CCC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-2-8-3-4-19-12-7-13-10(5-9(8)12)11(15(16,17)18)6-14(21)20-13/h5-8,19H,2-4H2,1H3,(H,20,21)
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n/an/a 7.48E+3n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Transcriptional repression in HepG2 cells expressing human glucocorticoid receptor


J Med Chem 42: 210-2 (1999)


Article DOI: 10.1021/jm9806648
BindingDB Entry DOI: 10.7270/Q2F76D8W
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM18190
PNG
(6-ethyl-4-(trifluoromethyl)-1H,2H,6H,7H,8H,9H-pyri...)
Show SMILES CCC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C15H15F3N2O/c1-2-8-3-4-19-12-7-13-10(5-9(8)12)11(15(16,17)18)6-14(21)20-13/h5-8,19H,2-4H2,1H3,(H,20,21)
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n/an/an/an/a 4n/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonist activity against Human Androgen receptor expressed in CV-1 cells


J Med Chem 42: 210-2 (1999)


Article DOI: 10.1021/jm9806648
BindingDB Entry DOI: 10.7270/Q2F76D8W
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063113
PNG
(1,6,8,8-Tetramethyl-4-trifluoromethyl-6,7,8,9-tetr...)
Show SMILES CC1CC(C)(C)Nc2cc3n(C)c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-9-8-16(2,3)21-13-7-14-11(5-10(9)13)12(17(18,19)20)6-15(23)22(14)4/h5-7,9,21H,8H2,1-4H3
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n/an/a 73n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063109
PNG
(6-Ethyl-8,8-dimethyl-4-trifluoromethyl-6,7,8,9-tet...)
Show SMILES CCC1CC(C)(C)Nc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-4-9-8-16(2,3)22-14-7-13-11(5-10(9)14)12(17(18,19)20)6-15(23)21-13/h5-7,9,22H,4,8H2,1-3H3,(H,21,23)
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n/an/a 27n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063118
PNG
(3a,10-Dimethyl-7-trifluoromethyl-1,2,3a,4,5,10-hex...)
Show SMILES Cn1c2cc3N4CCCC4(C)CCc3cc2c(cc1=O)C(F)(F)F
Show InChI InChI=1S/C18H19F3N2O/c1-17-5-3-7-23(17)14-10-15-12(8-11(14)4-6-17)13(18(19,20)21)9-16(24)22(15)2/h8-10H,3-7H2,1-2H3
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n/an/a 27n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063108
PNG
(6,8,8-Trimethyl-4-trifluoromethyl-6,7,8,9-tetrahyd...)
Show SMILES CC1CC(C)(C)Nc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-8-7-15(2,3)21-13-6-12-10(4-9(8)13)11(16(17,18)19)5-14(22)20-12/h4-6,8,21H,7H2,1-3H3,(H,20,22)
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n/an/a 26n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063116
PNG
(1,6,8,8,10-Pentamethyl-4-trifluoromethyl-6,7,8,9-t...)
Show SMILES CC1CC(C)(C)Nc2c(C)c3n(C)c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C18H21F3N2O/c1-9-8-17(3,4)22-15-10(2)16-12(6-11(9)15)13(18(19,20)21)7-14(24)23(16)5/h6-7,9,22H,8H2,1-5H3
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n/an/a 31n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50063111
PNG
(1,8,8-Trimethyl-4-trifluoromethyl-6,7,8,9-tetrahyd...)
Show SMILES Cn1c2cc3NC(C)(C)CCc3cc2c(cc1=O)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-15(2)5-4-9-6-10-11(16(17,18)19)7-14(22)21(3)13(10)8-12(9)20-15/h6-8,20H,4-5H2,1-3H3
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n/an/a 36n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077107
PNG
(6-Ethyl-9-methyl-4-trifluoromethyl-6,7,8,9-tetrahy...)
Show SMILES CCC1CCN(C)c2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C16H17F3N2O/c1-3-9-4-5-21(2)14-8-13-11(6-10(9)14)12(16(17,18)19)7-15(22)20-13/h6-9H,3-5H2,1-2H3,(H,20,22)
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n/an/an/an/a 158n/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Agonist activity to the human androgen receptor (hAR) in CV-1 cells


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Androgen Receptor


(Homo sapiens (Human))
BDBM50077100
PNG
(6-Isobutyl-4-trifluoromethyl-6,7,8,9-tetrahydro-1H...)
Show SMILES CC(C)CC1CCNc2cc3[nH]c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O/c1-9(2)5-10-3-4-21-14-8-15-12(6-11(10)14)13(17(18,19)20)7-16(23)22-15/h6-10,21H,3-5H2,1-2H3,(H,22,23)
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n/an/a>1.00E+4n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human androgen receptor (hAR) in CV-1 cells was determined as a function of maximal inhibition of dihydrotestosterone u...


Bioorg Med Chem Lett 9: 1335-40 (1999)


Article DOI: 10.1016/s0960-894x(99)00186-9
BindingDB Entry DOI: 10.7270/Q2JM2B4G
More data for this
Ligand-Target Pair
Progesterone receptor


(Homo sapiens (Human))
BDBM50063116
PNG
(1,6,8,8,10-Pentamethyl-4-trifluoromethyl-6,7,8,9-t...)
Show SMILES CC1CC(C)(C)Nc2c(C)c3n(C)c(=O)cc(c3cc12)C(F)(F)F
Show InChI InChI=1S/C18H21F3N2O/c1-9-8-17(3,4)22-15-10(2)16-12(6-11(9)15)13(18(19,20)21)7-14(24)23(16)5/h6-7,9,22H,8H2,1-5H3
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n/an/a 2.93E+3n/an/an/an/an/an/a



Ligand Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Antagonistic activity against human progesterone receptor B (hPR-B) in co-transfected CV-1 cells.


J Med Chem 41: 623-39 (1998)


Article DOI: 10.1021/jm970699s
BindingDB Entry DOI: 10.7270/Q2VM4CZ6
More data for this
Ligand-Target Pair