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PubMed code 10762045

Compile data set for download or QSAR
Found 65 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
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087205
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-6,8-diiodo-2-[(E)-3...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C27H18Cl2F3I2NO4/c28-18-6-5-15(20(29)11-18)13-39-25-21(33)9-16-10-22(26(37)38)35(12-19(16)24(25)34)23(36)7-4-14-2-1-3-17(8-14)27(30,31)32/h1-9,11,22H,10,12-13H2,(H,37,38)/b7-4+/t22-/m0/s1
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n/an/a 1.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087187
PNG
((S)-2-[(E)-3-(2-Chloro-phenyl)-acryloyl]-7-(2,4-di...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1ccccc1Cl
Show InChI InChI=1S/C26H18Cl3I2NO4/c27-17-7-5-15(20(29)11-17)13-36-25-21(30)9-16-10-22(26(34)35)32(12-18(16)24(25)31)23(33)8-6-14-3-1-2-4-19(14)28/h1-9,11,22H,10,12-13H2,(H,34,35)/b8-6+/t22-/m0/s1
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n/an/a 1.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087179
PNG
((S)-2-[(E)-3-(3-Chloro-phenyl)-acryloyl]-7-(2,6-di...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3c(Cl)cccc3Cl)c(I)c2CN1C(=O)\C=C\c1cccc(Cl)c1
Show InChI InChI=1S/C26H18Cl3I2NO4/c27-16-4-1-3-14(9-16)7-8-23(33)32-12-17-15(11-22(32)26(34)35)10-21(30)25(24(17)31)36-13-18-19(28)5-2-6-20(18)29/h1-10,22H,11-13H2,(H,34,35)/b8-7+/t22-/m0/s1
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n/an/a 2.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087234
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-2-[(E)-3-(3,5-dichl...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1cc(Cl)cc(Cl)c1
Show InChI InChI=1S/C26H17Cl4I2NO4/c27-16-3-2-14(20(30)10-16)12-37-25-21(31)7-15-8-22(26(35)36)33(11-19(15)24(25)32)23(34)4-1-13-5-17(28)9-18(29)6-13/h1-7,9-10,22H,8,11-12H2,(H,35,36)/b4-1+/t22-/m0/s1
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n/an/a 2.30E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087231
PNG
((S)-2-[(E)-3-(4-Bromo-phenyl)-acryloyl]-7-(2,4-dic...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1ccc(Br)cc1
Show InChI InChI=1S/C26H18BrCl2I2NO4/c27-17-5-1-14(2-6-17)3-8-23(33)32-12-19-16(10-22(32)26(34)35)9-21(30)25(24(19)31)36-13-15-4-7-18(28)11-20(15)29/h1-9,11,22H,10,12-13H2,(H,34,35)/b8-3+/t22-/m0/s1
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n/an/a 2.30E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087191
PNG
((S)-2-[(E)-3-(2-Chloro-phenyl)-acryloyl]-7-(3-chlo...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCCCCl)c(I)c2CN1C(=O)\C=C\c1ccccc1Cl
Show InChI InChI=1S/C22H19Cl2I2NO4/c23-8-3-9-31-21-17(25)10-14-11-18(22(29)30)27(12-15(14)20(21)26)19(28)7-6-13-4-1-2-5-16(13)24/h1-2,4-7,10,18H,3,8-9,11-12H2,(H,29,30)/b7-6+/t18-/m0/s1
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n/an/a 2.70E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087225
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-6,8-diiodo-2-((E)-3...)
Show SMILES Cc1ccc(\C=C\C(=O)N2Cc3c(I)c(OCc4ccc(Cl)cc4Cl)c(I)cc3C[C@H]2C(O)=O)cc1
Show InChI InChI=1S/C27H21Cl2I2NO4/c1-15-2-4-16(5-3-15)6-9-24(33)32-13-20-18(11-23(32)27(34)35)10-22(30)26(25(20)31)36-14-17-7-8-19(28)12-21(17)29/h2-10,12,23H,11,13-14H2,1H3,(H,34,35)/b9-6+/t23-/m0/s1
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n/an/a 2.70E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087227
PNG
((S)-6,8-Diiodo-7-(4-trifluoromethyl-benzyloxy)-2-[...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(cc3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccccc1C(F)(F)F
Show InChI InChI=1S/C28H19F6I2NO4/c29-27(30,31)18-8-5-15(6-9-18)14-41-25-21(35)11-17-12-22(26(39)40)37(13-19(17)24(25)36)23(38)10-7-16-3-1-2-4-20(16)28(32,33)34/h1-11,22H,12-14H2,(H,39,40)/b10-7+/t22-/m0/s1
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n/an/a 2.70E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087189
PNG
((S)-7-Benzyloxycarbonylmethoxy-2-[(E)-3-(2,4-dichl...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCC(=O)OCc3ccccc3)c(I)c2CN1C(=O)\C=C\c1ccc(Cl)cc1Cl
Show InChI InChI=1S/C28H21Cl2I2NO6/c29-19-8-6-17(21(30)12-19)7-9-24(34)33-13-20-18(11-23(33)28(36)37)10-22(31)27(26(20)32)39-15-25(35)38-14-16-4-2-1-3-5-16/h1-10,12,23H,11,13-15H2,(H,36,37)/b9-7+/t23-/m0/s1
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n/an/a 2.80E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087199
PNG
((S)-2-[(E)-3-(3-Fluoro-phenyl)-acryloyl]-6,8-diiod...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(cc3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1cccc(F)c1
Show InChI InChI=1S/C27H19F4I2NO4/c28-19-3-1-2-15(10-19)6-9-23(35)34-13-20-17(12-22(34)26(36)37)11-21(32)25(24(20)33)38-14-16-4-7-18(8-5-16)27(29,30)31/h1-11,22H,12-14H2,(H,36,37)/b9-6+/t22-/m0/s1
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n/an/a 3.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087188
PNG
((S)-2-(2-Chloro-pyridine-3-carbonyl)-6,8-diiodo-7-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)c1cccnc1Cl
Show InChI InChI=1S/C24H16ClF3I2N2O4/c25-21-15(5-2-6-31-21)22(33)32-10-16-13(9-18(32)23(34)35)8-17(29)20(19(16)30)36-11-12-3-1-4-14(7-12)24(26,27)28/h1-8,18H,9-11H2,(H,34,35)/t18-/m0/s1
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n/an/a 3.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087173
PNG
((S)-6,8-Diiodo-2-((E)-3-p-tolyl-acryloyl)-7-(3-tri...)
Show SMILES Cc1ccc(\C=C\C(=O)N2Cc3c(I)c(OCc4cccc(c4)C(F)(F)F)c(I)cc3C[C@H]2C(O)=O)cc1
Show InChI InChI=1S/C28H22F3I2NO4/c1-16-5-7-17(8-6-16)9-10-24(35)34-14-21-19(13-23(34)27(36)37)12-22(32)26(25(21)33)38-15-18-3-2-4-20(11-18)28(29,30)31/h2-12,23H,13-15H2,1H3,(H,36,37)/b10-9+/t23-/m0/s1
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n/an/a 3.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087196
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-2-[(E)-3-(3,4-dichl...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C26H17Cl4I2NO4/c27-16-4-3-14(19(29)10-16)12-37-25-21(31)8-15-9-22(26(35)36)33(11-17(15)24(25)32)23(34)6-2-13-1-5-18(28)20(30)7-13/h1-8,10,22H,9,11-12H2,(H,35,36)/b6-2+/t22-/m0/s1
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n/an/a 3.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087213
PNG
((S)-2-[(E)-3-(4-Chloro-phenyl)-acryloyl]-6,8-diiod...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(cc3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccc(Cl)cc1
Show InChI InChI=1S/C27H19ClF3I2NO4/c28-19-8-3-15(4-9-19)5-10-23(35)34-13-20-17(12-22(34)26(36)37)11-21(32)25(24(20)33)38-14-16-1-6-18(7-2-16)27(29,30)31/h1-11,22H,12-14H2,(H,36,37)/b10-5+/t22-/m0/s1
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n/an/a 3.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087183
PNG
((S)-2-((E)-3-2,4-Dioxa-bicyclo[3.3.1]nona-1(8),5(9...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(cc3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccc2OCOc1c2
Show InChI InChI=1S/C28H20F3I2NO6/c29-28(30,31)18-5-1-15(2-6-18)13-38-26-21(32)9-17-10-22(27(36)37)34(12-20(17)25(26)33)24(35)8-4-16-3-7-19-11-23(16)40-14-39-19/h1-9,11,22H,10,12-14H2,(H,36,37)/b8-4+/t22-/m0/s1
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n/an/a 3.20E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087224
PNG
((S)-2-[(E)-3-(2-Bromo-phenyl)-acryloyl]-7-(3-chlor...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCCCCl)c(I)c2CN1C(=O)\C=C\c1ccccc1Br
Show InChI InChI=1S/C22H19BrClI2NO4/c23-16-5-2-1-4-13(16)6-7-19(28)27-12-15-14(11-18(27)22(29)30)10-17(25)21(20(15)26)31-9-3-8-24/h1-2,4-7,10,18H,3,8-9,11-12H2,(H,29,30)/b7-6+/t18-/m0/s1
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n/an/a 3.30E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087206
PNG
((S)-2-[(E)-3-(2-Bromo-phenyl)-acryloyl]-7-(2,4-dic...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1ccccc1Br
Show InChI InChI=1S/C26H18BrCl2I2NO4/c27-19-4-2-1-3-14(19)6-8-23(33)32-12-18-16(10-22(32)26(34)35)9-21(30)25(24(18)31)36-13-15-5-7-17(28)11-20(15)29/h1-9,11,22H,10,12-13H2,(H,34,35)/b8-6+/t22-/m0/s1
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n/an/a 3.30E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087204
PNG
((3S)-7-[(2,6-dichlorophenyl)methoxy]-6,8-diiodo-2-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3c(Cl)cccc3Cl)c(I)c2CN1C(=O)\C=C\c1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C27H18Cl2F3I2NO4/c28-19-5-2-6-20(29)18(19)13-39-25-21(33)10-15-11-22(26(37)38)35(12-17(15)24(25)34)23(36)8-7-14-3-1-4-16(9-14)27(30,31)32/h1-10,22H,11-13H2,(H,37,38)/b8-7+/t22-/m0/s1
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n/an/a 3.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087197
PNG
((S)-2-[(E)-3-(2-Fluoro-phenyl)-acryloyl]-6,8-diiod...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccccc1F
Show InChI InChI=1S/C27H19F4I2NO4/c28-20-7-2-1-5-16(20)8-9-23(35)34-13-19-17(12-22(34)26(36)37)11-21(32)25(24(19)33)38-14-15-4-3-6-18(10-15)27(29,30)31/h1-11,22H,12-14H2,(H,36,37)/b9-8+/t22-/m0/s1
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n/an/a 3.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087203
PNG
((S)-6,8-Diiodo-2-((E)-3-p-tolyl-acryloyl)-7-(4-tri...)
Show SMILES Cc1ccc(\C=C\C(=O)N2Cc3c(I)c(OCc4ccc(cc4)C(F)(F)F)c(I)cc3C[C@H]2C(O)=O)cc1
Show InChI InChI=1S/C28H22F3I2NO4/c1-16-2-4-17(5-3-16)8-11-24(35)34-14-21-19(13-23(34)27(36)37)12-22(32)26(25(21)33)38-15-18-6-9-20(10-7-18)28(29,30)31/h2-12,23H,13-15H2,1H3,(H,36,37)/b11-8+/t23-/m0/s1
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n/an/a 3.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087208
PNG
((S)-2-[(E)-3-(4-Chloro-phenyl)-acryloyl]-7-(2,4-di...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1ccc(Cl)cc1
Show InChI InChI=1S/C26H18Cl3I2NO4/c27-17-5-1-14(2-6-17)3-8-23(33)32-12-19-16(10-22(32)26(34)35)9-21(30)25(24(19)31)36-13-15-4-7-18(28)11-20(15)29/h1-9,11,22H,10,12-13H2,(H,34,35)/b8-3+/t22-/m0/s1
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n/an/a 3.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087223
PNG
((S)-2-[(E)-3-(3-Chloro-phenyl)-acryloyl]-7-(2,4-di...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1cccc(Cl)c1
Show InChI InChI=1S/C26H18Cl3I2NO4/c27-17-3-1-2-14(8-17)4-7-23(33)32-12-19-16(10-22(32)26(34)35)9-21(30)25(24(19)31)36-13-15-5-6-18(28)11-20(15)29/h1-9,11,22H,10,12-13H2,(H,34,35)/b7-4+/t22-/m0/s1
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n/an/a 3.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087235
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-2-((Z)-2-fluoro-3-p...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)C(\F)=C\c1ccccc1
Show InChI InChI=1S/C26H18Cl2FI2NO4/c27-17-7-6-15(19(28)11-17)13-36-24-21(30)9-16-10-22(26(34)35)32(12-18(16)23(24)31)25(33)20(29)8-14-4-2-1-3-5-14/h1-9,11,22H,10,12-13H2,(H,34,35)/b20-8-/t22-/m0/s1
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n/an/a 3.60E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087198
PNG
((S)-6,8-Diiodo-7-(3-trifluoromethyl-benzyloxy)-2-[...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccccc1C(F)(F)F
Show InChI InChI=1S/C28H19F6I2NO4/c29-27(30,31)18-6-3-4-15(10-18)14-41-25-21(35)11-17-12-22(26(39)40)37(13-19(17)24(25)36)23(38)9-8-16-5-1-2-7-20(16)28(32,33)34/h1-11,22H,12-14H2,(H,39,40)/b9-8+/t22-/m0/s1
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n/an/a 3.60E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087186
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-6,8-diiodo-2-((E)-2...)
Show SMILES C\C(=C/c1ccccc1)C(=O)N1Cc2c(I)c(OCc3ccc(Cl)cc3Cl)c(I)cc2C[C@H]1C(O)=O
Show InChI InChI=1S/C27H21Cl2I2NO4/c1-15(9-16-5-3-2-4-6-16)26(33)32-13-20-18(11-23(32)27(34)35)10-22(30)25(24(20)31)36-14-17-7-8-19(28)12-21(17)29/h2-10,12,23H,11,13-14H2,1H3,(H,34,35)/b15-9+/t23-/m0/s1
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n/an/a 4.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087181
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-2-[(E)-3-(3-fluoro-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1cccc(F)c1
Show InChI InChI=1S/C26H18Cl2FI2NO4/c27-17-6-5-15(20(28)11-17)13-36-25-21(30)9-16-10-22(26(34)35)32(12-19(16)24(25)31)23(33)7-4-14-2-1-3-18(29)8-14/h1-9,11,22H,10,12-13H2,(H,34,35)/b7-4+/t22-/m0/s1
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n/an/a 4.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087202
PNG
((S)-2-[(E)-3-(3-Chloro-phenyl)-acryloyl]-6,8-diiod...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1cccc(Cl)c1
Show InChI InChI=1S/C27H19ClF3I2NO4/c28-19-6-2-3-15(10-19)7-8-23(35)34-13-20-17(12-22(34)26(36)37)11-21(32)25(24(20)33)38-14-16-4-1-5-18(9-16)27(29,30)31/h1-11,22H,12-14H2,(H,36,37)/b8-7+/t22-/m0/s1
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n/an/a 4.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087200
PNG
((S)-2-[(E)-3-(3-Bromo-phenyl)-acryloyl]-7-(2,4-dic...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1cccc(Br)c1
Show InChI InChI=1S/C26H18BrCl2I2NO4/c27-17-3-1-2-14(8-17)4-7-23(33)32-12-19-16(10-22(32)26(34)35)9-21(30)25(24(19)31)36-13-15-5-6-18(28)11-20(15)29/h1-9,11,22H,10,12-13H2,(H,34,35)/b7-4+/t22-/m0/s1
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n/an/a 4.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087201
PNG
((S)-7-(2-Fluoro-benzyloxy)-6,8-diiodo-2-[(E)-3-(3-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccccc3F)c(I)c2CN1C(=O)\C=C\c1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C27H19F4I2NO4/c28-20-7-2-1-5-16(20)14-38-25-21(32)11-17-12-22(26(36)37)34(13-19(17)24(25)33)23(35)9-8-15-4-3-6-18(10-15)27(29,30)31/h1-11,22H,12-14H2,(H,36,37)/b9-8+/t22-/m0/s1
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n/an/a 4.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087190
PNG
((S)-2-[(E)-3-(3-Fluoro-phenyl)-acryloyl]-6,8-diiod...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1cccc(F)c1
Show InChI InChI=1S/C27H19F4I2NO4/c28-19-6-2-3-15(10-19)7-8-23(35)34-13-20-17(12-22(34)26(36)37)11-21(32)25(24(20)33)38-14-16-4-1-5-18(9-16)27(29,30)31/h1-11,22H,12-14H2,(H,36,37)/b8-7+/t22-/m0/s1
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n/an/a 4.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087195
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-6,8-diiodo-2-[(E)-3...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C26H18Cl2I2N2O6/c27-17-5-4-15(20(28)11-17)13-38-25-21(29)9-16-10-22(26(34)35)31(12-19(16)24(25)30)23(33)8-3-14-1-6-18(7-2-14)32(36)37/h1-9,11,22H,10,12-13H2,(H,34,35)/b8-3+/t22-/m0/s1
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n/an/a 4.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087228
PNG
((S)-2-(2-Chloro-pyridine-3-carbonyl)-7-(2,6-dichlo...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3c(Cl)cccc3Cl)c(I)c2CN1C(=O)c1cccnc1Cl
Show InChI InChI=1S/C23H15Cl3I2N2O4/c24-15-4-1-5-16(25)14(15)10-34-20-17(27)7-11-8-18(23(32)33)30(9-13(11)19(20)28)22(31)12-3-2-6-29-21(12)26/h1-7,18H,8-10H2,(H,32,33)/t18-/m0/s1
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n/an/a 4.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087232
PNG
((S)-7-(2,6-Dichloro-benzyloxy)-2-[(E)-3-(3-fluoro-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3c(Cl)cccc3Cl)c(I)c2CN1C(=O)\C=C\c1cccc(F)c1
Show InChI InChI=1S/C26H18Cl2FI2NO4/c27-19-5-2-6-20(28)18(19)13-36-25-21(30)10-15-11-22(26(34)35)32(12-17(15)24(25)31)23(33)8-7-14-3-1-4-16(29)9-14/h1-10,22H,11-13H2,(H,34,35)/b8-7+/t22-/m0/s1
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n/an/a 4.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087226
PNG
((S)-7-Benzyloxycarbonylmethoxy-2-[(E)-3-(2-bromo-p...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCC(=O)OCc3ccccc3)c(I)c2CN1C(=O)\C=C\c1ccccc1Br
Show InChI InChI=1S/C28H22BrI2NO6/c29-21-9-5-4-8-18(21)10-11-24(33)32-14-20-19(13-23(32)28(35)36)12-22(30)27(26(20)31)38-16-25(34)37-15-17-6-2-1-3-7-17/h1-12,23H,13-16H2,(H,35,36)/b11-10+/t23-/m0/s1
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n/an/a 4.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087193
PNG
((S)-6,8-Diiodo-2-(3-phenyl-propionyl)-7-(3-trifluo...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)CCc1ccccc1
Show InChI InChI=1S/C27H22F3I2NO4/c28-27(29,30)19-8-4-7-17(11-19)15-37-25-21(31)12-18-13-22(26(35)36)33(14-20(18)24(25)32)23(34)10-9-16-5-2-1-3-6-16/h1-8,11-12,22H,9-10,13-15H2,(H,35,36)/t22-/m0/s1
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n/an/a 5.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087230
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-6,8-diiodo-2-(3-phe...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)CCc1ccccc1
Show InChI InChI=1S/C26H21Cl2I2NO4/c27-18-8-7-16(20(28)12-18)14-35-25-21(29)10-17-11-22(26(33)34)31(13-19(17)24(25)30)23(32)9-6-15-4-2-1-3-5-15/h1-5,7-8,10,12,22H,6,9,11,13-14H2,(H,33,34)/t22-/m0/s1
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n/an/a 5.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087176
PNG
((S)-6,8-Diiodo-2-[(E)-3-(4-nitro-phenyl)-acryloyl]...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C27H19F3I2N2O6/c28-27(29,30)18-3-1-2-16(10-18)14-40-25-21(31)11-17-12-22(26(36)37)33(13-20(17)24(25)32)23(35)9-6-15-4-7-19(8-5-15)34(38)39/h1-11,22H,12-14H2,(H,36,37)/b9-6+/t22-/m0/s1
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n/an/a 5.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087209
PNG
((S)-6,8-Diiodo-7-(3-trifluoromethyl-benzyloxy)-2-[...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1cccc(c1)C(F)(F)F
Show InChI InChI=1S/C28H19F6I2NO4/c29-27(30,31)18-5-1-3-15(9-18)7-8-23(38)37-13-20-17(12-22(37)26(39)40)11-21(35)25(24(20)36)41-14-16-4-2-6-19(10-16)28(32,33)34/h1-11,22H,12-14H2,(H,39,40)/b8-7+/t22-/m0/s1
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n/an/a 5.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087233
PNG
((S)-7-(3-Chloro-propoxy)-2-[(E)-3-(2,4-dichloro-ph...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCCCCl)c(I)c2CN1C(=O)\C=C\c1ccc(Cl)cc1Cl
Show InChI InChI=1S/C22H18Cl3I2NO4/c23-6-1-7-32-21-17(26)8-13-9-18(22(30)31)28(11-15(13)20(21)27)19(29)5-3-12-2-4-14(24)10-16(12)25/h2-5,8,10,18H,1,6-7,9,11H2,(H,30,31)/b5-3+/t18-/m0/s1
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n/an/a 5.20E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087174
PNG
((S)-2-[(E)-3-(2-Fluoro-phenyl)-acryloyl]-6,8-diiod...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(cc3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccccc1F
Show InChI InChI=1S/C27H19F4I2NO4/c28-20-4-2-1-3-16(20)7-10-23(35)34-13-19-17(12-22(34)26(36)37)11-21(32)25(24(19)33)38-14-15-5-8-18(9-6-15)27(29,30)31/h1-11,22H,12-14H2,(H,36,37)/b10-7+/t22-/m0/s1
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n/an/a 5.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087222
PNG
((S)-7-(2,6-Dichloro-benzyloxy)-2-[(E)-3-(3,4-dichl...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3c(Cl)cccc3Cl)c(I)c2CN1C(=O)\C=C\c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C26H17Cl4I2NO4/c27-17-2-1-3-18(28)16(17)12-37-25-21(31)9-14-10-22(26(35)36)33(11-15(14)24(25)32)23(34)7-5-13-4-6-19(29)20(30)8-13/h1-9,22H,10-12H2,(H,35,36)/b7-5+/t22-/m0/s1
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n/an/a 5.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087215
PNG
((S)-6,8-Diiodo-2-[(E)-3-(4-nitro-phenyl)-acryloyl]...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(cc3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C27H19F3I2N2O6/c28-27(29,30)18-6-1-16(2-7-18)14-40-25-21(31)11-17-12-22(26(36)37)33(13-20(17)24(25)32)23(35)10-5-15-3-8-19(9-4-15)34(38)39/h1-11,22H,12-14H2,(H,36,37)/b10-5+/t22-/m0/s1
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n/an/a 5.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087184
PNG
((S)-6,8-Diiodo-7-(4-trifluoromethyl-benzyloxy)-2-[...)
Show SMILES COc1cc(\C=C\C(=O)N2Cc3c(I)c(OCc4ccc(cc4)C(F)(F)F)c(I)cc3C[C@H]2C(O)=O)cc(OC)c1OC
Show InChI InChI=1S/C30H26F3I2NO7/c1-40-23-10-17(11-24(41-2)28(23)42-3)6-9-25(37)36-14-20-18(13-22(36)29(38)39)12-21(34)27(26(20)35)43-15-16-4-7-19(8-5-16)30(31,32)33/h4-12,22H,13-15H2,1-3H3,(H,38,39)/b9-6+/t22-/m0/s1
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n/an/a 5.70E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087185
PNG
((S)-2-((E)-3-2,4-Dioxa-bicyclo[3.3.1]nona-1(8),5(9...)
Show SMILES COc1cccc(COc2c(I)cc3C[C@H](N(Cc3c2I)C(=O)\C=C\c2ccc3OCOc2c3)C(O)=O)c1
Show InChI InChI=1S/C28H23I2NO7/c1-35-19-4-2-3-16(9-19)14-36-27-22(29)10-18-11-23(28(33)34)31(13-21(18)26(27)30)25(32)8-6-17-5-7-20-12-24(17)38-15-37-20/h2-10,12,23H,11,13-15H2,1H3,(H,33,34)/b8-6+/t23-/m0/s1
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n/an/a 5.80E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087210
PNG
((S)-6,8-Diiodo-7-(3-methoxy-benzyloxy)-2-[(E)-3-(4...)
Show SMILES COc1cccc(COc2c(I)cc3C[C@H](N(Cc3c2I)C(=O)\C=C\c2ccc(cc2)[N+]([O-])=O)C(O)=O)c1
Show InChI InChI=1S/C27H22I2N2O7/c1-37-20-4-2-3-17(11-20)15-38-26-22(28)12-18-13-23(27(33)34)30(14-21(18)25(26)29)24(32)10-7-16-5-8-19(9-6-16)31(35)36/h2-12,23H,13-15H2,1H3,(H,33,34)/b10-7+/t23-/m0/s1
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n/an/a 5.90E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087211
PNG
((S)-2-[(E)-3-(3-Chloro-phenyl)-acryloyl]-7-(2-fluo...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccccc3F)c(I)c2CN1C(=O)\C=C\c1cccc(Cl)c1
Show InChI InChI=1S/C26H19ClFI2NO4/c27-18-6-3-4-15(10-18)8-9-23(32)31-13-19-17(12-22(31)26(33)34)11-21(29)25(24(19)30)35-14-16-5-1-2-7-20(16)28/h1-11,22H,12-14H2,(H,33,34)/b9-8+/t22-/m0/s1
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n/an/a 6.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087194
PNG
((S)-7-(2,4-Dichloro-benzyloxy)-2-((E)-3-2,4-dioxa-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)\C=C\c1ccc2OCOc1c2
Show InChI InChI=1S/C27H19Cl2I2NO6/c28-17-4-1-15(20(29)9-17)12-36-26-21(30)7-16-8-22(27(34)35)32(11-19(16)25(26)31)24(33)6-3-14-2-5-18-10-23(14)38-13-37-18/h1-7,9-10,22H,8,11-13H2,(H,34,35)/b6-3+/t22-/m0/s1
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n/an/a 6.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087216
PNG
((S)-6,8-Diiodo-7-(3-methoxy-benzyloxy)-2-((E)-3-p-...)
Show SMILES COc1cccc(COc2c(I)cc3C[C@H](N(Cc3c2I)C(=O)\C=C\c2ccc(C)cc2)C(O)=O)c1
Show InChI InChI=1S/C28H25I2NO5/c1-17-6-8-18(9-7-17)10-11-25(32)31-15-22-20(14-24(31)28(33)34)13-23(29)27(26(22)30)36-16-19-4-3-5-21(12-19)35-2/h3-13,24H,14-16H2,1-2H3,(H,33,34)/b11-10+/t24-/m0/s1
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n/an/a 6.20E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087221
PNG
((S)-2-((E)-3-2,4-Dioxa-bicyclo[3.3.1]nona-1(8),5(9...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccc2OCOc1c2
Show InChI InChI=1S/C28H20F3I2NO6/c29-28(30,31)18-3-1-2-15(8-18)13-38-26-21(32)9-17-10-22(27(36)37)34(12-20(17)25(26)33)24(35)7-5-16-4-6-19-11-23(16)40-14-39-19/h1-9,11,22H,10,12-14H2,(H,36,37)/b7-5+/t22-/m0/s1
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n/an/a 6.60E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087236
PNG
((S)-2-[(E)-3-(4-Bromo-phenyl)-acryloyl]-7-(3-chlor...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCCCCl)c(I)c2CN1C(=O)\C=C\c1ccc(Br)cc1
Show InChI InChI=1S/C22H19BrClI2NO4/c23-15-5-2-13(3-6-15)4-7-19(28)27-12-16-14(11-18(27)22(29)30)10-17(25)21(20(16)26)31-9-1-8-24/h2-7,10,18H,1,8-9,11-12H2,(H,29,30)/b7-4+/t18-/m0/s1
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n/an/a 7.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087214
PNG
((S)-7-Benzyloxycarbonylmethoxy-2-[(E)-3-(2-chloro-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCC(=O)OCc3ccccc3)c(I)c2CN1C(=O)\C=C\c1ccccc1Cl
Show InChI InChI=1S/C28H22ClI2NO6/c29-21-9-5-4-8-18(21)10-11-24(33)32-14-20-19(13-23(32)28(35)36)12-22(30)27(26(20)31)38-16-25(34)37-15-17-6-2-1-3-7-17/h1-12,23H,13-16H2,(H,35,36)/b11-10+/t23-/m0/s1
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n/an/a 7.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087178
PNG
((S)-2-[(E)-3-(3-Bromo-phenyl)-acryloyl]-7-(3-chlor...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCCCCl)c(I)c2CN1C(=O)\C=C\c1cccc(Br)c1
Show InChI InChI=1S/C22H19BrClI2NO4/c23-15-4-1-3-13(9-15)5-6-19(28)27-12-16-14(11-18(27)22(29)30)10-17(25)21(20(16)26)31-8-2-7-24/h1,3-6,9-10,18H,2,7-8,11-12H2,(H,29,30)/b6-5+/t18-/m0/s1
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n/an/a 7.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087175
PNG
((S)-2-[(E)-3-(4-Chloro-phenyl)-acryloyl]-6,8-diiod...)
Show SMILES COc1cccc(COc2c(I)cc3C[C@H](N(Cc3c2I)C(=O)\C=C\c2ccc(Cl)cc2)C(O)=O)c1
Show InChI InChI=1S/C27H22ClI2NO5/c1-35-20-4-2-3-17(11-20)15-36-26-22(29)12-18-13-23(27(33)34)31(14-21(18)25(26)30)24(32)10-7-16-5-8-19(28)9-6-16/h2-12,23H,13-15H2,1H3,(H,33,34)/b10-7+/t23-/m0/s1
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n/an/a 7.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087219
PNG
((S)-7-(2-Fluoro-benzyloxy)-2-[(E)-3-(3-fluoro-phen...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccccc3F)c(I)c2CN1C(=O)\C=C\c1cccc(F)c1
Show InChI InChI=1S/C26H19F2I2NO4/c27-18-6-3-4-15(10-18)8-9-23(32)31-13-19-17(12-22(31)26(33)34)11-21(29)25(24(19)30)35-14-16-5-1-2-7-20(16)28/h1-11,22H,12-14H2,(H,33,34)/b9-8+/t22-/m0/s1
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n/an/a 7.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087220
PNG
((S)-2-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-6,8-d...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3cccc(c3)C(F)(F)F)c(I)c2CN1C(=O)\C=C\c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C27H18Cl2F3I2NO4/c28-19-6-4-14(9-20(19)29)5-7-23(36)35-12-18-16(11-22(35)26(37)38)10-21(33)25(24(18)34)39-13-15-2-1-3-17(8-15)27(30,31)32/h1-10,22H,11-13H2,(H,37,38)/b7-5+/t22-/m0/s1
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n/an/a 7.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087180
PNG
((S)-2-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-7-(2-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccccc3F)c(I)c2CN1C(=O)\C=C\c1ccc(Cl)c(Cl)c1
Show InChI InChI=1S/C26H18Cl2FI2NO4/c27-18-7-5-14(9-19(18)28)6-8-23(33)32-12-17-16(11-22(32)26(34)35)10-21(30)25(24(17)31)36-13-15-3-1-2-4-20(15)29/h1-10,22H,11-13H2,(H,34,35)/b8-6+/t22-/m0/s1
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n/an/a 7.50E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087212
PNG
((S)-7-(2-Fluoro-benzyloxy)-6,8-diiodo-2-(3-phenyl-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccccc3F)c(I)c2CN1C(=O)CCc1ccccc1
Show InChI InChI=1S/C26H22FI2NO4/c27-20-9-5-4-8-17(20)15-34-25-21(28)12-18-13-22(26(32)33)30(14-19(18)24(25)29)23(31)11-10-16-6-2-1-3-7-16/h1-9,12,22H,10-11,13-15H2,(H,32,33)/t22-/m0/s1
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n/an/a 8.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087192
PNG
((S)-7-Benzyloxycarbonylmethoxy-2-[(E)-3-(3-bromo-p...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCC(=O)OCc3ccccc3)c(I)c2CN1C(=O)\C=C\c1cccc(Br)c1
Show InChI InChI=1S/C28H22BrI2NO6/c29-20-8-4-7-17(11-20)9-10-24(33)32-14-21-19(13-23(32)28(35)36)12-22(30)27(26(21)31)38-16-25(34)37-15-18-5-2-1-3-6-18/h1-12,23H,13-16H2,(H,35,36)/b10-9+/t23-/m0/s1
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n/an/a 9.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087207
PNG
((S)-7-Benzyloxycarbonylmethoxy-2-[(E)-3-(4-bromo-p...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCC(=O)OCc3ccccc3)c(I)c2CN1C(=O)\C=C\c1ccc(Br)cc1
Show InChI InChI=1S/C28H22BrI2NO6/c29-20-9-6-17(7-10-20)8-11-24(33)32-14-21-19(13-23(32)28(35)36)12-22(30)27(26(21)31)38-16-25(34)37-15-18-4-2-1-3-5-18/h1-12,23H,13-16H2,(H,35,36)/b11-8+/t23-/m0/s1
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n/an/a 9.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087229
PNG
((S)-7-Benzyloxycarbonylmethoxy-2-((Z)-2-fluoro-3-p...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCC(=O)OCc3ccccc3)c(I)c2CN1C(=O)C(\F)=C\c1ccccc1
Show InChI InChI=1S/C28H22FI2NO6/c29-21(11-17-7-3-1-4-8-17)27(34)32-14-20-19(13-23(32)28(35)36)12-22(30)26(25(20)31)38-16-24(33)37-15-18-9-5-2-6-10-18/h1-12,23H,13-16H2,(H,35,36)/b21-11-/t23-/m0/s1
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n/an/a 9.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087172
PNG
((S)-2-(2-Chloro-pyridine-3-carbonyl)-7-(2-fluoro-b...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccccc3F)c(I)c2CN1C(=O)c1cccnc1Cl
Show InChI InChI=1S/C23H16ClFI2N2O4/c24-21-14(5-3-7-28-21)22(30)29-10-15-13(9-18(29)23(31)32)8-17(26)20(19(15)27)33-11-12-4-1-2-6-16(12)25/h1-8,18H,9-11H2,(H,31,32)/t18-/m0/s1
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n/an/a 9.00E+4n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087218
PNG
((S)-2-(2-Chloro-pyridine-3-carbonyl)-7-(2,4-dichlo...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3ccc(Cl)cc3Cl)c(I)c2CN1C(=O)c1cccnc1Cl
Show InChI InChI=1S/C23H15Cl3I2N2O4/c24-13-4-3-11(16(25)8-13)10-34-20-17(27)6-12-7-18(23(32)33)30(9-15(12)19(20)28)22(31)14-2-1-5-29-21(14)26/h1-6,8,18H,7,9-10H2,(H,32,33)/t18-/m0/s1
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n/an/a>1.00E+5n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087217
PNG
((S)-7-(3-Chloro-propoxy)-2-((Z)-2-fluoro-3-phenyl-...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCCCCl)c(I)c2CN1C(=O)C(\F)=C\c1ccccc1
Show InChI InChI=1S/C22H19ClFI2NO4/c23-7-4-8-31-20-17(25)10-14-11-18(22(29)30)27(12-15(14)19(20)26)21(28)16(24)9-13-5-2-1-3-6-13/h1-3,5-6,9-10,18H,4,7-8,11-12H2,(H,29,30)/b16-9-/t18-/m0/s1
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n/an/a 1.00E+5n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087182
PNG
(2-Cyclopentanecarbonyl-7-(2,6-dichloro-benzyloxy)-...)
Show SMILES OC(=O)C1Cc2cc(I)c(OCc3c(Cl)cccc3Cl)c(I)c2CN1C(=O)C1CCCC1
Show InChI InChI=1S/C23H21Cl2I2NO4/c24-16-6-3-7-17(25)15(16)11-32-21-18(26)8-13-9-19(23(30)31)28(10-14(13)20(21)27)22(29)12-4-1-2-5-12/h3,6-8,12,19H,1-2,4-5,9-11H2,(H,30,31)
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n/an/a 1.00E+5n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50087177
PNG
((S)-7-(2,6-Dichloro-benzyloxy)-6,8-diiodo-2-(3-phe...)
Show SMILES OC(=O)[C@@H]1Cc2cc(I)c(OCc3c(Cl)cccc3Cl)c(I)c2CN1C(=O)CCc1ccccc1
Show InChI InChI=1S/C26H21Cl2I2NO4/c27-19-7-4-8-20(28)18(19)14-35-25-21(29)11-16-12-22(26(33)34)31(13-17(16)24(25)30)23(32)10-9-15-5-2-1-3-6-15/h1-8,11,22H,9-10,12-14H2,(H,33,34)/t22-/m0/s1
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n/an/a>1.00E+5n/an/an/an/an/an/a



Pharmacia & Upjohn Company

Curated by ChEMBL


Assay Description
Compound was measured for its inhibitory activity against Cell division cycle 25B


Bioorg Med Chem Lett 10: 649-52 (2000)


BindingDB Entry DOI: 10.7270/Q2KS6QRN
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%