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Compile Data Set for Download or QSAR

Found 265 hits with Last Name = 'chiu' and Initial = 'fc'   
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
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM8610
PNG
(1-[4-(4-{[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1H-imi...)
Show SMILES [H][C@]1(COc2ccc(cc2)N2CCN(CC2)C(C)=O)CO[C@@](Cn2ccnc2)(O1)c1ccc(Cl)cc1Cl |r|
Show InChI InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m0/s1
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n/an/a 1n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 in human liver microsomes using testosterone as substrate after 5 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM8610
PNG
(1-[4-(4-{[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1H-imi...)
Show SMILES [H][C@]1(COc2ccc(cc2)N2CCN(CC2)C(C)=O)CO[C@@](Cn2ccnc2)(O1)c1ccc(Cl)cc1Cl |r|
Show InChI InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m0/s1
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n/an/a 4n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 in human liver microsomes using midazolam as substrate after 4 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM50121975
PNG
((6-Methoxy-quinolin-4-yl)-(5-vinyl-1-aza-bicyclo[2...)
Show SMILES COc1ccc2nccc([C@H](O)[C@H]3C[C@@H]4CCN3C[C@@H]4C=C)c2c1 |r,THB:20:19:12.13:16.15,10:12:18.19:16.15|
Show InChI InChI=1S/C20H24N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3/t13-,14-,19+,20-/m0/s1
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n/an/a 9n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2D6 in human liver microsomes using dextromethorphan as substrate after 10 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydroorotate dehydrogenase (quinone), mitochondrial


(Rattus norvegicus (rat))
BDBM50018011
PNG
(Aubagio | CHEBI:68540 | HMR-1726 | TERIFLUNOMIDE)
Show SMILES C\C(O)=C(/C#N)C(=O)Nc1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C12H9F3N2O2/c1-7(18)10(6-16)11(19)17-9-4-2-8(3-5-9)12(13,14)15/h2-5,18H,1H3,(H,17,19)/b10-7-
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n/an/a 17n/an/an/an/an/an/a



University of Washington

Curated by ChEMBL


Assay Description
Inhibition of C-terminal His6-tagged rat DHODH expressed in Escherichia coli BL21(DE3) cells using L-DHO as substrate by DCIP dye based assay


J Med Chem 63: 4929-4956 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00311
BindingDB Entry DOI: 10.7270/Q2M90D6Z
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50305505
PNG
(CHEMBL227855 | OZ-209 | dispiro[adamantane-2,2'-[1...)
Show SMILES NC[C@H]1CC[C@]2(CC1)OO[C@@]1(O2)C2CC3CC(C2)CC1C3 |r,wU:10.10,2.1,wD:5.12,TLB:20:19:15.14.13:17,11:10:16.17.18:14.13.20,9:10:15.14.13:17,THB:20:14:17:10.18.19,11:10:15.14.13:17,9:10:16.17.18:14.13.20,15:14:10:16.17.18,15:16:10:14.13.20,(42.83,-6.44,;42.06,-5.09,;40.52,-5.09,;39.74,-6.41,;38.21,-6.41,;37.44,-5.07,;38.21,-3.74,;39.75,-3.75,;36.96,-3.61,;35.42,-3.62,;34.95,-5.09,;36.2,-5.99,;33.79,-6.1,;32.6,-5.28,;32.09,-3.96,;30.33,-3.92,;31.64,-4.76,;32.15,-6.19,;32.83,-3.69,;34.45,-3.65,;33.19,-2.96,)|
Show InChI InChI=1S/C17H27NO3/c18-10-11-1-3-16(4-2-11)19-17(21-20-16)14-6-12-5-13(8-14)9-15(17)7-12/h11-15H,1-10,18H2/t11-,12?,13?,14?,15?,16+,17-
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n/an/a 110n/an/an/an/an/an/a



University of Nebraska Medical Center

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19


Bioorg Med Chem Lett 20: 563-6 (2010)


Article DOI: 10.1016/j.bmcl.2009.11.088
BindingDB Entry DOI: 10.7270/Q2RJ4JKQ
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase (quinone), mitochondrial


(Mus musculus)
BDBM50018011
PNG
(Aubagio | CHEBI:68540 | HMR-1726 | TERIFLUNOMIDE)
Show SMILES C\C(O)=C(/C#N)C(=O)Nc1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C12H9F3N2O2/c1-7(18)10(6-16)11(19)17-9-4-2-8(3-5-9)12(13,14)15/h2-5,18H,1H3,(H,17,19)/b10-7-
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n/an/a 110n/an/an/an/an/an/a



University of Washington

Curated by ChEMBL


Assay Description
Inhibition of C-terminal His6-tagged mouse DHODH expressed in Escherichia coli BL21(DE3) cells using L-DHO as substrate by DCIP dye based assay


J Med Chem 63: 4929-4956 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00311
BindingDB Entry DOI: 10.7270/Q2M90D6Z
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Androgen receptor


(Homo sapiens (Human))
BDBM50550378
PNG
(CHEMBL4799175)
Show SMILES CCN1C(=O)N(C(=O)C1(C)C)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 140n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550361
PNG
(CHEMBL4793070)
Show SMILES Fc1ccc(cc1C(F)(F)F)N1C(=O)CNC1=O
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n/an/a 260n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550377
PNG
(CHEMBL4758277)
Show SMILES CC1(C)N(CC#N)C(=O)N(C1=O)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 290n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase (quinone), mitochondrial


(Homo sapiens (Human))
BDBM50018011
PNG
(Aubagio | CHEBI:68540 | HMR-1726 | TERIFLUNOMIDE)
Show SMILES C\C(O)=C(/C#N)C(=O)Nc1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C12H9F3N2O2/c1-7(18)10(6-16)11(19)17-9-4-2-8(3-5-9)12(13,14)15/h2-5,18H,1H3,(H,17,19)/b10-7-
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n/an/a 300n/an/an/an/an/an/a



University of Washington

Curated by ChEMBL


Assay Description
Inhibition of C-terminal His6-tagged human DHODH expressed in Escherichia coli BL21(DE3) cells using L-DHO as substrate by DCIP dye based assay


J Med Chem 63: 4929-4956 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00311
BindingDB Entry DOI: 10.7270/Q2M90D6Z
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Androgen receptor


(Homo sapiens (Human))
BDBM50135912
PNG
(5,5-Dimethyl-3-(alpha,alpha,alpha-trifluoro-4-nitr...)
Show SMILES CC1(C)NC(=O)N(C1=O)c1ccc(c(c1)C(F)(F)F)[N+]([O-])=O
Show InChI InChI=1S/C12H10F3N3O4/c1-11(2)9(19)17(10(20)16-11)6-3-4-8(18(21)22)7(5-6)12(13,14)15/h3-5H,1-2H3,(H,16,20)
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n/an/a 600n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 2C9


(Homo sapiens (Human))
BDBM50090677
PNG
(4-Amino-N-(2-phenyl-2H-pyrazol-3-yl)-benzenesulfon...)
Show SMILES Nc1ccc(cc1)S(=O)(=O)Nc1ccnn1-c1ccccc1
Show InChI InChI=1S/C15H14N4O2S/c16-12-6-8-14(9-7-12)22(20,21)18-15-10-11-17-19(15)13-4-2-1-3-5-13/h1-11,18H,16H2
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n/an/a 740n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2C9 in human liver microsomes using tolbutamide as substrate after 20 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550354
PNG
(CHEMBL4787997)
Show SMILES CC1(C)CC(=O)N(C1=O)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 910n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550357
PNG
(CHEMBL4755665)
Show SMILES Fc1ccc(cc1C(F)(F)F)N1C(=O)NC2(CCCC2)C1=O
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n/an/a 990n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50180847
PNG
(CHEMBL3408523)
Show SMILES CC1=CSC(OCC(F)(F)F)(c2noc(=O)n12)c1ccc(Br)cc1 |t:1|
Show InChI InChI=1S/C14H10BrF3N2O3S/c1-8-6-24-14(22-7-13(16,17)18,9-2-4-10(15)5-3-9)11-19-23-12(21)20(8)11/h2-6H,7H2,1H3
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n/an/a 1.00E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 in human liver microsomes using (S)-mephenytoin as substrate after 40 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM85509
PNG
(CAS_55142-85-3 | NSC_5472 | Ticlopidine)
Show SMILES Clc1ccccc1CN1CCc2sccc2C1
Show InChI InChI=1S/C14H14ClNS/c15-13-4-2-1-3-11(13)9-16-7-5-14-12(10-16)6-8-17-14/h1-4,6,8H,5,7,9-10H2
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n/an/a 1.30E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 in human liver microsomes using (S)-mephenytoin as substrate after 40 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Cytochrome P450 1A2


(Homo sapiens (Human))
BDBM50236897
PNG
(3-(furan-2-ylmethyl)-1,8-dimethyl-1H-purine-2,6(3H...)
Show SMILES Cc1nc2n(Cc3ccco3)c(=O)n(C)c(=O)c2[nH]1
Show InChI InChI=1S/C12H12N4O3/c1-7-13-9-10(14-7)16(6-8-4-3-5-19-8)12(18)15(2)11(9)17/h3-5H,6H2,1-2H3,(H,13,14)
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n/an/a 1.30E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP1A2 in human liver microsomes using phenacetin as substrate after 30 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550379
PNG
(CHEMBL4778974)
Show SMILES CN1C(=O)N(C(=O)C1(C)C)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 1.30E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550372
PNG
(CHEMBL4750103)
Show SMILES CC1(C)NC(=O)N(C1=O)c1ccc(Cl)c(c1)C(F)(F)F
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n/an/a 1.30E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550366
PNG
(CHEMBL4778298)
Show SMILES CC1(C)NC(=O)N(C1=O)c1ccnc2ccccc12
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n/an/a 1.30E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50180846
PNG
(CHEMBL211204)
Show SMILES CCOC1(SC=C(C)n2c1noc2=O)c1ccc(Br)cc1 |t:5|
Show InChI InChI=1S/C14H13BrN2O3S/c1-3-19-14(10-4-6-11(15)7-5-10)12-16-20-13(18)17(12)9(2)8-21-14/h4-8H,3H2,1-2H3
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Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 in human liver microsomes using (S)-mephenytoin as substrate after 40 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50201426
PNG
(dispiro[adamantane-2,2'-[1,3,5]trioxolane-4',1''-c...)
Show SMILES NC[C@H]1CC[C@]2(CC1)OO[C@@]1(O2)C2CC3CC(C2)CC1C3 |w:14.15,16.18,12.14,19.21,wU:10.10,5.8,2.1,TLB:17:12:15.16.18:20,THB:11:10:15.16.18:20,9:10:15.16.18:20,10:12:15:18.19.20,10:19:15:13.17.12,TEB:17:16:20:13.12.10,18:19:13:15.16.17,(13.45,-13.89,;13.42,-12.35,;12.07,-11.6,;10.75,-12.4,;9.41,-11.66,;9.37,-10.12,;10.69,-9.32,;12.04,-10.06,;9.17,-8.58,;7.66,-8.3,;6.92,-9.66,;7.98,-10.78,;5.82,-10.73,;4.59,-9.98,;4.01,-8.7,;2.26,-8.74,;3.61,-9.51,;4.2,-10.91,;4.73,-8.39,;6.34,-8.26,;5.06,-7.64,)|
Show InChI InChI=1S/C17H27NO3/c18-10-11-1-3-16(4-2-11)19-17(21-20-16)14-6-12-5-13(8-14)9-15(17)7-12/h11-15H,1-10,18H2/t11-,12?,13?,14?,15?,16+,17-
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n/an/a 1.80E+3n/an/an/an/an/an/a



University of Nebraska Medical Center

Curated by ChEMBL


Assay Description
Inhibition of hERG by patch clamp assay


Bioorg Med Chem Lett 17: 1260-5 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.007
BindingDB Entry DOI: 10.7270/Q2N017B8
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550353
PNG
(CHEMBL4790269)
Show SMILES CC1(C)OC(=O)N(C1=O)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 2.10E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase (quinone), mitochondrial


(Mus musculus)
BDBM50365230
PNG
(CHEMBL1956285 | US9238653, Table 5, Compound 10)
Show SMILES Cc1cc(Nc2ccc(cc2)S(F)(F)(F)(F)F)n2nc(nc2n1)C(C)(F)F
Show InChI InChI=1S/C14H12F7N5S/c1-8-7-11(26-13(22-8)24-12(25-26)14(2,15)16)23-9-3-5-10(6-4-9)27(17,18,19,20)21/h3-7,23H,1-2H3
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n/an/a 2.10E+3n/an/an/an/an/an/a



University of Washington

Curated by ChEMBL


Assay Description
Inhibition of C-terminal His6-tagged mouse DHODH expressed in Escherichia coli BL21(DE3) cells using L-DHO as substrate by DCIP dye based assay


J Med Chem 63: 4929-4956 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00311
BindingDB Entry DOI: 10.7270/Q2M90D6Z
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550376
PNG
(CHEMBL4786505)
Show SMILES CC1(C)N(CCc2ccccc2)C(=O)N(C1=O)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 2.40E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50180841
PNG
(CHEMBL3819606)
Show SMILES CC1=CSC(OCC(F)(F)F)(c2noc(=O)n12)c1ccccc1 |t:1|
Show InChI InChI=1S/C14H11F3N2O3S/c1-9-7-23-14(21-8-13(15,16)17,10-5-3-2-4-6-10)11-18-22-12(20)19(9)11/h2-7H,8H2,1H3
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n/an/a 2.40E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 in human liver microsomes using (S)-mephenytoin as substrate after 40 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50180842
PNG
(CHEMBL3818643)
Show SMILES CCOC1(SC=C(C)n2c1noc2=O)c1ccc(OC)cc1 |t:5|
Show InChI InChI=1S/C15H16N2O4S/c1-4-20-15(11-5-7-12(19-3)8-6-11)13-16-21-14(18)17(13)10(2)9-22-15/h5-9H,4H2,1-3H3
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n/an/a 2.50E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 in human liver microsomes using (S)-mephenytoin as substrate after 40 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50201425
PNG
(2-({dispiro[adamantane-2,2'-[1,3,5]trioxolane-4',1...)
Show SMILES NC(=O)CNC[C@H]1CC[C@]2(CC1)OO[C@@]1(O2)C2CC3CC(C2)CC1C3 |w:18.19,20.22,16.18,23.25,wU:14.14,9.12,6.5,TLB:21:16:19.20.22:24,THB:15:14:19.20.22:24,13:14:19.20.22:24,14:16:19:22.23.24,14:23:19:17.21.16,TEB:21:20:24:17.16.14,22:23:17:19.20.21,(25.77,-11.15,;27.09,-10.36,;28.44,-11.11,;27.07,-8.82,;25.73,-8.06,;25.71,-6.52,;24.36,-5.77,;23.04,-6.56,;21.7,-5.81,;21.68,-4.27,;23,-3.47,;24.34,-4.23,;21.49,-2.73,;19.98,-2.44,;19.23,-3.79,;20.28,-4.92,;18.12,-4.85,;16.9,-4.09,;16.32,-2.81,;14.58,-2.84,;15.92,-3.62,;16.5,-5.02,;17.05,-2.51,;18.66,-2.39,;17.38,-1.76,)|
Show InChI InChI=1S/C19H30N2O4/c20-17(22)11-21-10-12-1-3-18(4-2-12)23-19(25-24-18)15-6-13-5-14(8-15)9-16(19)7-13/h12-16,21H,1-11H2,(H2,20,22)/t12-,13?,14?,15?,16?,18+,19-
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n/an/a 2.70E+3n/an/an/an/an/an/a



University of Nebraska Medical Center

Curated by ChEMBL


Assay Description
Inhibition of hERG by patch clamp assay


Bioorg Med Chem Lett 17: 1260-5 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.007
BindingDB Entry DOI: 10.7270/Q2N017B8
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550350
PNG
(CHEMBL4786811)
Show SMILES CC1(C)N(C(=O)NC1=O)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 2.80E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 1A2


(Homo sapiens (Human))
BDBM50180846
PNG
(CHEMBL211204)
Show SMILES CCOC1(SC=C(C)n2c1noc2=O)c1ccc(Br)cc1 |t:5|
Show InChI InChI=1S/C14H13BrN2O3S/c1-3-19-14(10-4-6-11(15)7-5-10)12-16-20-13(18)17(12)9(2)8-21-14/h4-8H,3H2,1-2H3
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n/an/a 2.90E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP1A2 in human liver microsomes using phenacetin as substrate after 30 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550347
PNG
(CHEMBL4572306)
Show SMILES CC(C)(NC(=O)Nc1ccc(F)c(c1)C(F)(F)F)C(O)=O
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n/an/a 3.10E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550355
PNG
(CHEMBL4778185)
Show SMILES Fc1ccc(cc1C(F)(F)F)N1C(=O)C2CCCN2C1=O
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n/an/a 3.50E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50180844
PNG
(CHEMBL3818560)
Show SMILES CCOC1(Sc2ccccc2-n2c1noc2=O)c1ccc(OC)cc1
Show InChI InChI=1S/C18H16N2O4S/c1-3-23-18(12-8-10-13(22-2)11-9-12)16-19-24-17(21)20(16)14-6-4-5-7-15(14)25-18/h4-11H,3H2,1-2H3
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n/an/a 3.60E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 in human liver microsomes using (S)-mephenytoin as substrate after 40 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550370
PNG
(CHEMBL4799429)
Show SMILES CC1(C)NC(=O)N(C1=O)c1ccc(F)c(c1)C#N
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n/an/a 3.70E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550368
PNG
(CHEMBL4782426)
Show SMILES CC1(C)NC(=O)N(C1=O)c1ccncc1
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n/an/a 3.80E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50495154
PNG
(CHEMBL3104490)
Show SMILES CS(=O)(=O)c1ccc(cc1)N1CCN(CC1)C(=O)C(c1ccc(Cl)cc1)c1cccnc1
Show InChI InChI=1S/C24H24ClN3O3S/c1-32(30,31)22-10-8-21(9-11-22)27-13-15-28(16-14-27)24(29)23(19-3-2-12-26-17-19)18-4-6-20(25)7-5-18/h2-12,17,23H,13-16H2,1H3
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n/an/a 4.00E+3n/an/an/an/an/an/a



Epichem Pty Ltd.

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 in human liver microsomes assessed as 6beta-hydroxylation of testosterone


J Med Chem 56: 10158-70 (2013)


Article DOI: 10.1021/jm401610c
BindingDB Entry DOI: 10.7270/Q2VH5RT9
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM50180846
PNG
(CHEMBL211204)
Show SMILES CCOC1(SC=C(C)n2c1noc2=O)c1ccc(Br)cc1 |t:5|
Show InChI InChI=1S/C14H13BrN2O3S/c1-3-19-14(10-4-6-11(15)7-5-10)12-16-20-13(18)17(12)9(2)8-21-14/h4-8H,3H2,1-2H3
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n/an/a 4.10E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2D6 in human liver microsomes using dextromethorphan as substrate after 10 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550356
PNG
(CHEMBL4747499)
Show SMILES Fc1ccc(cc1C(F)(F)F)N1C(=O)NC2(CCCCC2)C1=O
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n/an/a 4.20E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550362
PNG
(CHEMBL4743529)
Show SMILES CC1(C)NC(=O)N(Cc2ccc(F)c(c2)C(F)(F)F)C1=O
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n/an/a 4.20E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550374
PNG
(CHEMBL4748557)
Show SMILES CC1(C)N(C(=O)N(C1=O)c1ccc(F)c(c1)C(F)(F)F)S(=O)(=O)c1ccccc1
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n/an/a 4.30E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase (quinone), mitochondrial


(Rattus norvegicus (rat))
BDBM50365230
PNG
(CHEMBL1956285 | US9238653, Table 5, Compound 10)
Show SMILES Cc1cc(Nc2ccc(cc2)S(F)(F)(F)(F)F)n2nc(nc2n1)C(C)(F)F
Show InChI InChI=1S/C14H12F7N5S/c1-8-7-11(26-13(22-8)24-12(25-26)14(2,15)16)23-9-3-5-10(6-4-9)27(17,18,19,20)21/h3-7,23H,1-2H3
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n/an/a 4.40E+3n/an/an/an/an/an/a



University of Washington

Curated by ChEMBL


Assay Description
Inhibition of C-terminal His6-tagged rat DHODH expressed in Escherichia coli BL21(DE3) cells using L-DHO as substrate by DCIP dye based assay


J Med Chem 63: 4929-4956 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00311
BindingDB Entry DOI: 10.7270/Q2M90D6Z
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550380
PNG
(CHEMBL4465426)
Show SMILES CC1(C)NC(=O)N(C1=O)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 4.40E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550367
PNG
(CHEMBL4748422)
Show SMILES CC1(C)NC(=O)N(C1=O)c1ccnc(c1)C(F)(F)F
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n/an/a 4.50E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 2C19


(Homo sapiens (Human))
BDBM50180840
PNG
(CHEMBL3819185)
Show SMILES CCOC1(SC=C(C)n2c1noc2=O)c1ccccc1 |t:5|
Show InChI InChI=1S/C14H14N2O3S/c1-3-18-14(11-7-5-4-6-8-11)12-15-19-13(17)16(12)10(2)9-20-14/h4-9H,3H2,1-2H3
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n/an/a 4.80E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP2C19 in human liver microsomes using (S)-mephenytoin as substrate after 40 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550358
PNG
(CHEMBL4793158)
Show SMILES CC1(CO)NC(=O)N(C1=O)c1ccc(F)c(c1)C(F)(F)F
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n/an/a 4.80E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 1A2


(Homo sapiens (Human))
BDBM50180847
PNG
(CHEMBL3408523)
Show SMILES CC1=CSC(OCC(F)(F)F)(c2noc(=O)n12)c1ccc(Br)cc1 |t:1|
Show InChI InChI=1S/C14H10BrF3N2O3S/c1-8-6-24-14(22-7-13(16,17)18,9-2-4-10(15)5-3-9)11-19-23-12(21)20(8)11/h2-6H,7H2,1H3
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n/an/a 5.00E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP1A2 in human liver microsomes using phenacetin as substrate after 30 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50495150
PNG
(CHEMBL3104537)
Show SMILES FC(F)(F)c1ccc(cc1)N(C1CCN(CC1)c1ccccc1C#N)c1cccnc1
Show InChI InChI=1S/C24H21F3N4/c25-24(26,27)19-7-9-20(10-8-19)31(22-5-3-13-29-17-22)21-11-14-30(15-12-21)23-6-2-1-4-18(23)16-28/h1-10,13,17,21H,11-12,14-15H2
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n/an/a 5.20E+3n/an/an/an/an/an/a



Epichem Pty Ltd.

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4 in human liver microsomes assessed as 6beta-hydroxylation of testosterone


J Med Chem 56: 10158-70 (2013)


Article DOI: 10.1021/jm401610c
BindingDB Entry DOI: 10.7270/Q2VH5RT9
More data for this
Ligand-Target Pair
Cytochrome P450 1A2


(Homo sapiens (Human))
BDBM50180842
PNG
(CHEMBL3818643)
Show SMILES CCOC1(SC=C(C)n2c1noc2=O)c1ccc(OC)cc1 |t:5|
Show InChI InChI=1S/C15H16N2O4S/c1-4-20-15(11-5-7-12(19-3)8-6-11)13-16-21-14(18)17(13)10(2)9-22-15/h5-9H,4H2,1-3H3
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n/an/a 5.20E+3n/an/an/an/an/an/a



Universit£ di Perugia

Curated by ChEMBL


Assay Description
Inhibition of CYP1A2 in human liver microsomes using phenacetin as substrate after 30 mins by LC-MS analysis


J Med Chem 59: 3340-52 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00030
BindingDB Entry DOI: 10.7270/Q29K4D50
More data for this
Ligand-Target Pair
Androgen receptor


(Homo sapiens (Human))
BDBM50550359
PNG
(CHEMBL4763136)
Show SMILES FC(F)c1cc(ccc1F)N1C(=O)N[C@@H](C1=O)c1ccccc1 |r|
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n/an/a 5.30E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of wild-type androgen receptor in human LAPC4 cells assessed as inhibition of DHT-induced luciferase activity measured after 24 hrs by luc...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2M0492B
More data for this
Ligand-Target Pair
Cytochrome P450 3A4/3A5


(Homo sapiens (Human))
BDBM50538344
PNG
(CHEMBL4633246)
Show SMILES Cc1c(Cc2ccc(nc2)C(F)(F)F)c[nH]c1C(=O)NC1CC1
Show InChI InChI=1S/C16H16F3N3O/c1-9-11(8-21-14(9)15(23)22-12-3-4-12)6-10-2-5-13(20-7-10)16(17,18)19/h2,5,7-8,12,21H,3-4,6H2,1H3,(H,22,23)
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n/an/a 5.50E+3n/an/an/an/an/an/a



University of Washington

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4/5 in human liver microsomes using midazolam as substrate preincubated for 30 mins followed by substrate addition and measured af...


J Med Chem 63: 4929-4956 (2020)


Article DOI: 10.1021/acs.jmedchem.0c00311
BindingDB Entry DOI: 10.7270/Q2M90D6Z
More data for this
Ligand-Target Pair
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