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8 molecules are shown

Wt: 409.3
BDBM1542
Wt: 427.3
BDBM15343
Wt: 355.3
BDBM16111
Purchase
Wt: 355.3
BDBM50137290
Wt: 409.3
BDBM50137292
Wt: 387.3
BDBM50137303
Wt: 373.3
BDBM50173152
Wt: 371.3
BDBM50173153

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 16 hits for monomerid = 1542,15343,16111,50137290,50137292,50137303,50173152,50173153   
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
HIV-1 Reverse Transcriptase


(Human immunodeficiency virus type 1)
BDBM1542
PNG
(2-({2-fluoro-4-[3-(trifluoromethoxy)phenyl]phenyl}...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1ccc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H15F4NO4/c21-16-10-12(11-3-1-4-13(9-11)29-20(22,23)24)7-8-17(16)25-18(26)14-5-2-6-15(14)19(27)28/h1,3-4,7-10H,2,5-6H2,(H,25,26)(H,27,28)
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n/an/a 400n/an/an/an/an/an/a



Boehringer Ingelheim Pharmaceuticals Inc.



Assay Description
The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.


J Med Chem 38: 4830-8 (1995)


Article DOI: 10.1021/jm00024a010
BindingDB Entry DOI: 10.7270/Q23B5XBJ
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM15343
PNG
(2-({2,6-difluoro-4-[3-(trifluoromethoxy)phenyl]phe...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1c(F)cc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H14F5NO4/c21-15-8-11(10-3-1-4-12(7-10)30-20(23,24)25)9-16(22)17(15)26-18(27)13-5-2-6-14(13)19(28)29/h1,3-4,7-9H,2,5-6H2,(H,26,27)(H,28,29)
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n/an/a 33n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
Inhibition of N-terminally truncated recombinant human dihydroorotate dehydrogenase using in vitro enzyme assay


Bioorg Med Chem Lett 15: 4854-7 (2005)


Article DOI: 10.1016/j.bmcl.2005.07.053
BindingDB Entry DOI: 10.7270/Q2HX1C7N
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydroorotate Dehydrogenase (DHODH)


(Homo sapiens (human))
BDBM16111
PNG
(2-{[2-fluoro-4-(3-methoxyphenyl)phenyl]carbamoyl}c...)
Show SMILES COc1cccc(c1)-c1ccc(NC(=O)C2=C(CCC2)C(O)=O)c(F)c1
Show InChI InChI=1S/C20H18FNO4/c1-26-14-5-2-4-12(10-14)13-8-9-18(17(21)11-13)22-19(23)15-6-3-7-16(15)20(24)25/h2,4-5,8-11H,3,6-7H2,1H3,(H,22,23)(H,24,25)
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n/an/a 134n/an/an/an/a8.025



4SC AG



Assay Description
The assays were carried out by using a colorimetric DCIP method, which uses the colorimetric reagent 2, 6-dichlorophenolindophenol as the final elect...


Bioorg Med Chem Lett 16: 267-70 (2006)


Article DOI: 10.1016/j.bmcl.2005.10.011
BindingDB Entry DOI: 10.7270/Q2CJ8BQ4
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM1542
PNG
(2-({2-fluoro-4-[3-(trifluoromethoxy)phenyl]phenyl}...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1ccc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H15F4NO4/c21-16-10-12(11-3-1-4-13(9-11)29-20(22,23)24)7-8-17(16)25-18(26)14-5-2-6-15(14)19(27)28/h1,3-4,7-10H,2,5-6H2,(H,25,26)(H,27,28)
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n/an/a 280n/an/an/an/a8.030



4SC AG



Assay Description
The assays were carried out by using a colorimetric DCIP method, which uses the colorimetric reagent 2, 6-dichlorophenolindophenol as the final elect...


J Med Chem 49: 1239-47 (2006)


Article DOI: 10.1021/jm0506975
BindingDB Entry DOI: 10.7270/Q2571988
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM15343
PNG
(2-({2,6-difluoro-4-[3-(trifluoromethoxy)phenyl]phe...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1c(F)cc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H14F5NO4/c21-15-8-11(10-3-1-4-12(7-10)30-20(23,24)25)9-16(22)17(15)26-18(27)13-5-2-6-14(13)19(28)29/h1,3-4,7-9H,2,5-6H2,(H,26,27)(H,28,29)
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n/an/a 33n/an/an/an/a8.030



4SC AG



Assay Description
The assays were carried out by using a colorimetric DCIP method, which uses the colorimetric reagent 2, 6-dichlorophenolindophenol as the final elect...


J Med Chem 49: 1239-47 (2006)


Article DOI: 10.1021/jm0506975
BindingDB Entry DOI: 10.7270/Q2571988
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM1542
PNG
(2-({2-fluoro-4-[3-(trifluoromethoxy)phenyl]phenyl}...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1ccc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H15F4NO4/c21-16-10-12(11-3-1-4-13(9-11)29-20(22,23)24)7-8-17(16)25-18(26)14-5-2-6-15(14)19(27)28/h1,3-4,7-10H,2,5-6H2,(H,25,26)(H,27,28)
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n/an/a 280n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against human dihydroorotate dehydrogenase (DHODH)


Bioorg Med Chem Lett 14: 55-8 (2003)


Article DOI: 10.1016/j.bmcl.2003.10.021
BindingDB Entry DOI: 10.7270/Q2XS5TS2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM50137290
PNG
(2-(3-Fluoro-4'-methoxy-biphenyl-4-ylcarbamoyl)-cyc...)
Show SMILES COc1ccc(cc1)-c1ccc(NC(=O)C2=C(CCC2)C(O)=O)c(F)c1
Show InChI InChI=1S/C20H18FNO4/c1-26-14-8-5-12(6-9-14)13-7-10-18(17(21)11-13)22-19(23)15-3-2-4-16(15)20(24)25/h5-11H,2-4H2,1H3,(H,22,23)(H,24,25)
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n/an/a 1.70E+3n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against human dihydroorotate dehydrogenase (DHODH)


Bioorg Med Chem Lett 14: 55-8 (2003)


Article DOI: 10.1016/j.bmcl.2003.10.021
BindingDB Entry DOI: 10.7270/Q2XS5TS2
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM50137292
PNG
(2-(3-Fluoro-4'-trifluoromethoxy-biphenyl-4-ylcarba...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1ccc(cc1F)-c1ccc(OC(F)(F)F)cc1
Show InChI InChI=1S/C20H15F4NO4/c21-16-10-12(11-4-7-13(8-5-11)29-20(22,23)24)6-9-17(16)25-18(26)14-2-1-3-15(14)19(27)28/h4-10H,1-3H2,(H,25,26)(H,27,28)
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n/an/a 5.70E+3n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against human dihydroorotate dehydrogenase (DHODH)


Bioorg Med Chem Lett 14: 55-8 (2003)


Article DOI: 10.1016/j.bmcl.2003.10.021
BindingDB Entry DOI: 10.7270/Q2XS5TS2
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM50137303
PNG
(2-(3'-Ethoxy-3,5-difluoro-biphenyl-4-ylcarbamoyl)-...)
Show SMILES CCOc1cccc(c1)-c1cc(F)c(NC(=O)C2=C(CCC2)C(O)=O)c(F)c1
Show InChI InChI=1S/C21H19F2NO4/c1-2-28-14-6-3-5-12(9-14)13-10-17(22)19(18(23)11-13)24-20(25)15-7-4-8-16(15)21(26)27/h3,5-6,9-11H,2,4,7-8H2,1H3,(H,24,25)(H,26,27)
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n/an/a 17n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against human dihydroorotate dehydrogenase (DHODH)


Bioorg Med Chem Lett 14: 55-8 (2003)


Article DOI: 10.1016/j.bmcl.2003.10.021
BindingDB Entry DOI: 10.7270/Q2XS5TS2
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM15343
PNG
(2-({2,6-difluoro-4-[3-(trifluoromethoxy)phenyl]phe...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1c(F)cc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H14F5NO4/c21-15-8-11(10-3-1-4-12(7-10)30-20(23,24)25)9-16(22)17(15)26-18(27)13-5-2-6-14(13)19(28)29/h1,3-4,7-9H,2,5-6H2,(H,26,27)(H,28,29)
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n/an/a 33n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against human dihydroorotate dehydrogenase (DHODH)


Bioorg Med Chem Lett 14: 55-8 (2003)


Article DOI: 10.1016/j.bmcl.2003.10.021
BindingDB Entry DOI: 10.7270/Q2XS5TS2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydroorotate dehydrogenase


(Mus musculus)
BDBM15343
PNG
(2-({2,6-difluoro-4-[3-(trifluoromethoxy)phenyl]phe...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1c(F)cc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H14F5NO4/c21-15-8-11(10-3-1-4-12(7-10)30-20(23,24)25)9-16(22)17(15)26-18(27)13-5-2-6-14(13)19(28)29/h1,3-4,7-9H,2,5-6H2,(H,26,27)(H,28,29)
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n/an/a 2.00E+3n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
Inhibitory activity against mouse dihydroorotate dehydrogenase


Bioorg Med Chem Lett 15: 4854-7 (2005)


Article DOI: 10.1016/j.bmcl.2005.07.053
BindingDB Entry DOI: 10.7270/Q2HX1C7N
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM50173152
PNG
(2-(3,5-Difluoro-3'-methoxy-biphenyl-4-ylcarbamoyl)...)
Show SMILES COc1cccc(c1)-c1cc(F)c(NC(=O)C2=C(CCC2)C(O)=O)c(F)c1
Show InChI InChI=1S/C20H17F2NO4/c1-27-13-5-2-4-11(8-13)12-9-16(21)18(17(22)10-12)23-19(24)14-6-3-7-15(14)20(25)26/h2,4-5,8-10H,3,6-7H2,1H3,(H,23,24)(H,25,26)
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n/an/a 11n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
Inhibition of N-terminally truncated recombinant human dihydroorotate dehydrogenase using in vitro enzyme assay


Bioorg Med Chem Lett 15: 4854-7 (2005)


Article DOI: 10.1016/j.bmcl.2005.07.053
BindingDB Entry DOI: 10.7270/Q2HX1C7N
More data for this
Ligand-Target Pair
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM50173153
PNG
(2-(3-Fluoro-3'-methoxy-biphenyl-4-ylcarbamoyl)-5-h...)
Show SMILES COc1cccc(c1)-c1ccc(NC(=O)C2=C(C(O)CC2)C(O)=O)c(F)c1
Show InChI InChI=1S/C20H18FNO5/c1-27-13-4-2-3-11(9-13)12-5-7-16(15(21)10-12)22-19(24)14-6-8-17(23)18(14)20(25)26/h2-5,7,9-10,17,23H,6,8H2,1H3,(H,22,24)(H,25,26)
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n/an/a 680n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
Inhibition of N-terminally truncated recombinant human dihydroorotate dehydrogenase using in vitro enzyme assay


Bioorg Med Chem Lett 15: 4854-7 (2005)


Article DOI: 10.1016/j.bmcl.2005.07.053
BindingDB Entry DOI: 10.7270/Q2HX1C7N
More data for this
Ligand-Target Pair
Dihydroorotate Dehydrogenase (DHODH)


(Rattus norvegicus (rat))
BDBM15343
PNG
(2-({2,6-difluoro-4-[3-(trifluoromethoxy)phenyl]phe...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1c(F)cc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H14F5NO4/c21-15-8-11(10-3-1-4-12(7-10)30-20(23,24)25)9-16(22)17(15)26-18(27)13-5-2-6-14(13)19(28)29/h1,3-4,7-9H,2,5-6H2,(H,26,27)(H,28,29)
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n/an/a 504n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
Inhibitory activity against rat dihydroorotate dehydrogenase


Bioorg Med Chem Lett 15: 4854-7 (2005)


Article DOI: 10.1016/j.bmcl.2005.07.053
BindingDB Entry DOI: 10.7270/Q2HX1C7N
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Dihydroorotate dehydrogenase


(Homo sapiens (Human))
BDBM16111
PNG
(2-{[2-fluoro-4-(3-methoxyphenyl)phenyl]carbamoyl}c...)
Show SMILES COc1cccc(c1)-c1ccc(NC(=O)C2=C(CCC2)C(O)=O)c(F)c1
Show InChI InChI=1S/C20H18FNO4/c1-26-14-5-2-4-12(10-14)13-8-9-18(17(21)11-13)22-19(23)15-6-3-7-16(15)20(24)25/h2,4-5,8-11H,3,6-7H2,1H3,(H,22,23)(H,24,25)
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n/an/a 134n/an/an/an/an/an/a



4SC AG

Curated by ChEMBL


Assay Description
Inhibition of N-terminally truncated recombinant human dihydroorotate dehydrogenase using in vitro enzyme assay


Bioorg Med Chem Lett 15: 4854-7 (2005)


Article DOI: 10.1016/j.bmcl.2005.07.053
BindingDB Entry DOI: 10.7270/Q2HX1C7N
More data for this
Ligand-Target Pair
HIV-1 Reverse Transcriptase Mutant (Y181C)


(Human immunodeficiency virus type 1)
BDBM1542
PNG
(2-({2-fluoro-4-[3-(trifluoromethoxy)phenyl]phenyl}...)
Show SMILES OC(=O)C1=C(CCC1)C(=O)Nc1ccc(cc1F)-c1cccc(OC(F)(F)F)c1
Show InChI InChI=1S/C20H15F4NO4/c21-16-10-12(11-3-1-4-13(9-11)29-20(22,23)24)7-8-17(16)25-18(26)14-5-2-6-15(14)19(27)28/h1,3-4,7-10H,2,5-6H2,(H,25,26)(H,27,28)
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n/an/a>1.00E+3n/an/an/an/an/an/a



Boehringer Ingelheim Pharmaceuticals Inc.



Assay Description
The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro.


J Med Chem 38: 4830-8 (1995)


Article DOI: 10.1021/jm00024a010
BindingDB Entry DOI: 10.7270/Q23B5XBJ
More data for this
Ligand-Target Pair