BindingDB logo
myBDB logout

PubMed code 21050768

Compile data set for download or QSAR
Found 20 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Androgen receptor


(Homo sapiens (Human))
BDBM50317662
PNG
(3-[3-(3-Chloro-4-cyanophenyl)-5,5-dimethyl-4-oxo-2...)
Show SMILES CC1(C)N(CCCS(N)(=O)=O)C(=S)N(C1=O)c1ccc(C#N)c(Cl)c1
Show InChI InChI=1S/C15H17ClN4O3S2/c1-15(2)13(21)20(11-5-4-10(9-17)12(16)8-11)14(24)19(15)6-3-7-25(18,22)23/h4-5,8H,3,6-7H2,1-2H3,(H2,18,22,23)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 10n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331872
PNG
(5-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethy...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1cncc(c1)S(N)(=O)=O
Show InChI InChI=1S/C18H14F3N5O3S2/c1-17(2)15(27)25(11-4-3-10(7-22)14(6-11)18(19,20)21)16(30)26(17)12-5-13(9-24-8-12)31(23,28)29/h3-6,8-9H,1-2H3,(H2,23,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 30n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331871
PNG
(5-[3-(3-Chloro-4-cyanophenyl)-5,5-dimethyl-4-oxo-2...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(Cl)c1)c1cncc(c1)S(N)(=O)=O
Show InChI InChI=1S/C17H14ClN5O3S2/c1-17(2)15(24)22(11-4-3-10(7-19)14(18)6-11)16(27)23(17)12-5-13(9-21-8-12)28(20,25)26/h3-6,8-9H,1-2H3,(H2,20,25,26)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 50n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331870
PNG
(4-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethy...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1ccnc(c1)S(N)(=O)=O
Show InChI InChI=1S/C18H14F3N5O3S2/c1-17(2)15(27)25(11-4-3-10(9-22)13(7-11)18(19,20)21)16(30)26(17)12-5-6-24-14(8-12)31(23,28)29/h3-8H,1-2H3,(H2,23,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 80n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331866
PNG
(3-[3-(3-Chloro-4-cyanophenyl)-5,5-dimethyl-4-oxo-2...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(Cl)c1)c1cccc(c1)S(N)(=O)=O
Show InChI InChI=1S/C18H15ClN4O3S2/c1-18(2)16(24)22(12-7-6-11(10-20)15(19)9-12)17(27)23(18)13-4-3-5-14(8-13)28(21,25)26/h3-9H,1-2H3,(H2,21,25,26)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 100n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331867
PNG
(3-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethy...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1cccc(c1)S(N)(=O)=O
Show InChI InChI=1S/C19H15F3N4O3S2/c1-18(2)16(27)25(12-7-6-11(10-23)15(9-12)19(20,21)22)17(30)26(18)13-4-3-5-14(8-13)31(24,28)29/h3-9H,1-2H3,(H2,24,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 100n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331868
PNG
(6-[3-(3-Chloro-4-cyanophenyl)-5,5-dimethyl-4-oxo-2...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(Cl)c1)c1cccc(n1)S(N)(=O)=O
Show InChI InChI=1S/C17H14ClN5O3S2/c1-17(2)15(24)22(11-7-6-10(9-19)12(18)8-11)16(27)23(17)13-4-3-5-14(21-13)28(20,25)26/h3-8H,1-2H3,(H2,20,25,26)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 100n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331869
PNG
(6-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethy...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1cccc(n1)S(N)(=O)=O
Show InChI InChI=1S/C18H14F3N5O3S2/c1-17(2)15(27)25(11-7-6-10(9-22)12(8-11)18(19,20)21)16(30)26(17)13-4-3-5-14(24-13)31(23,28)29/h3-8H,1-2H3,(H2,23,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 100n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331865
PNG
(4-(3-Phenyl-4,4-dimethyl-5-oxo-2-thioxoimidazolidi...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1ccccc1
Show InChI InChI=1S/C19H14F3N3OS/c1-18(2)16(26)24(17(27)25(18)13-6-4-3-5-7-13)14-9-8-12(11-23)15(10-14)19(20,21)22/h3-10H,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 100n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331865
PNG
(4-(3-Phenyl-4,4-dimethyl-5-oxo-2-thioxoimidazolidi...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1ccccc1
Show InChI InChI=1S/C19H14F3N3OS/c1-18(2)16(26)24(17(27)25(18)13-6-4-3-5-7-13)14-9-8-12(11-23)15(10-14)19(20,21)22/h3-10H,1-2H3
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 200n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM18525
PNG
(Bicalutamide | CHEMBL409 | N-[4-cyano-3-(trifluoro...)
Show SMILES CC(O)(CS(=O)(=O)c1ccc(F)cc1)C(=O)Nc1ccc(C#N)c(c1)C(F)(F)F
Show InChI InChI=1S/C18H14F4N2O4S/c1-17(26,10-29(27,28)14-6-3-12(19)4-7-14)16(25)24-13-5-2-11(9-23)15(8-13)18(20,21)22/h2-8,26H,10H2,1H3,(H,24,25)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
UniChem

Patents


Similars

DrugBank
PDB
Article
PubMed
n/an/a 200n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Androgen receptor


(Homo sapiens (Human))
BDBM50317662
PNG
(3-[3-(3-Chloro-4-cyanophenyl)-5,5-dimethyl-4-oxo-2...)
Show SMILES CC1(C)N(CCCS(N)(=O)=O)C(=S)N(C1=O)c1ccc(C#N)c(Cl)c1
Show InChI InChI=1S/C15H17ClN4O3S2/c1-15(2)13(21)20(11-5-4-10(9-17)12(16)8-11)14(24)19(15)6-3-7-25(18,22)23/h4-5,8H,3,6-7H2,1-2H3,(H2,18,22,23)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 200n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331867
PNG
(3-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethy...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1cccc(c1)S(N)(=O)=O
Show InChI InChI=1S/C19H15F3N4O3S2/c1-18(2)16(27)25(12-7-6-11(10-23)15(9-12)19(20,21)22)17(30)26(18)13-4-3-5-14(8-13)31(24,28)29/h3-9H,1-2H3,(H2,24,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 300n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331866
PNG
(3-[3-(3-Chloro-4-cyanophenyl)-5,5-dimethyl-4-oxo-2...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(Cl)c1)c1cccc(c1)S(N)(=O)=O
Show InChI InChI=1S/C18H15ClN4O3S2/c1-18(2)16(24)22(12-7-6-11(10-20)15(19)9-12)17(27)23(18)13-4-3-5-14(8-13)28(21,25)26/h3-9H,1-2H3,(H2,21,25,26)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 400n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331868
PNG
(6-[3-(3-Chloro-4-cyanophenyl)-5,5-dimethyl-4-oxo-2...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(Cl)c1)c1cccc(n1)S(N)(=O)=O
Show InChI InChI=1S/C17H14ClN5O3S2/c1-17(2)15(24)22(11-7-6-10(9-19)12(18)8-11)16(27)23(17)13-4-3-5-14(21-13)28(20,25)26/h3-8H,1-2H3,(H2,20,25,26)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 600n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM18525
PNG
(Bicalutamide | CHEMBL409 | N-[4-cyano-3-(trifluoro...)
Show SMILES CC(O)(CS(=O)(=O)c1ccc(F)cc1)C(=O)Nc1ccc(C#N)c(c1)C(F)(F)F
Show InChI InChI=1S/C18H14F4N2O4S/c1-17(26,10-29(27,28)14-6-3-12(19)4-7-14)16(25)24-13-5-2-11(9-23)15(8-13)18(20,21)22/h2-8,26H,10H2,1H3,(H,24,25)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
PC cid
PC sid
PDB
UniChem

Patents


Similars

DrugBank
PDB
Article
PubMed
n/an/a 600n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at AR in human bicalutamide-resistant LNCAP cells assessed as inhibition of cell proliferation after 6 days


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Androgen receptor


(Homo sapiens (Human))
BDBM50331869
PNG
(6-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethy...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1cccc(n1)S(N)(=O)=O
Show InChI InChI=1S/C18H14F3N5O3S2/c1-17(2)15(27)25(11-7-6-10(9-22)12(8-11)18(19,20)21)16(30)26(17)13-4-3-5-14(24-13)31(23,28)29/h3-8H,1-2H3,(H2,23,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 700n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331870
PNG
(4-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethy...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1ccnc(c1)S(N)(=O)=O
Show InChI InChI=1S/C18H14F3N5O3S2/c1-17(2)15(27)25(11-4-3-10(9-22)13(7-11)18(19,20)21)16(30)26(17)12-5-6-24-14(8-12)31(23,28)29/h3-8H,1-2H3,(H2,23,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.00E+3n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331872
PNG
(5-[3-(4-Cyano-3-trifluoromethylphenyl)-5,5-dimethy...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(c1)C(F)(F)F)c1cncc(c1)S(N)(=O)=O
Show InChI InChI=1S/C18H14F3N5O3S2/c1-17(2)15(27)25(11-4-3-10(7-22)14(6-11)18(19,20)21)16(30)26(17)12-5-13(9-24-8-12)31(23,28)29/h3-6,8-9H,1-2H3,(H2,23,28,29)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.00E+3n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50331871
PNG
(5-[3-(3-Chloro-4-cyanophenyl)-5,5-dimethyl-4-oxo-2...)
Show SMILES CC1(C)N(C(=S)N(C1=O)c1ccc(C#N)c(Cl)c1)c1cncc(c1)S(N)(=O)=O
Show InChI InChI=1S/C17H14ClN5O3S2/c1-17(2)15(24)22(11-4-3-10(7-19)14(18)6-11)16(27)23(17)12-5-13(9-21-8-12)28(20,25)26/h3-6,8-9H,1-2H3,(H2,20,25,26)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.00E+3n/an/an/an/an/an/a



Chugai Pharmaceutical Co., Ltd

Curated by ChEMBL


Assay Description
Antagonist activity at human AR expressed in human HeLa cells co-transfected with MMTV-Luc-Hyg after 48 hrs by transient-luciferase reporter gene ass...


Bioorg Med Chem 18: 8150-7 (2010)


Article DOI: 10.1016/j.bmc.2010.10.023
BindingDB Entry DOI: 10.7270/Q29S1S1P
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%