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Compile Data Set for Download or QSAR

Found 957 hits of ic50 data for polymerid = 6311   
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))
BDBM50612011
PNG
(CHEMBL5288122)
PDB
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n/an/a 53n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50612010
PNG
(CHEMBL5271462)
PDB
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n/an/a 53n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50267086
PNG
(Adociaquinone B | CHEMBL476648)
Show SMILES C[C@@]12CCCc3coc(c13)C(=O)c1cc3C(=O)C4=NCCS(=O)(=O)C4C(=O)c3cc21 |r,t:19|
Show InChI InChI=1S/C22H17NO6S/c1-22-4-2-3-10-9-29-20(15(10)22)18(25)13-7-11-12(8-14(13)22)19(26)21-16(17(11)24)23-5-6-30(21,27)28/h7-9,21H,2-6H2,1H3/t21?,22-/m0/s1
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n/an/a 70n/an/an/an/an/an/a



Universit£ Paris Descartes

Curated by ChEMBL


Assay Description
Inhibition of human recombinant CDC25B


Bioorg Med Chem 16: 9040-9 (2008)


Article DOI: 10.1016/j.bmc.2008.08.009
BindingDB Entry DOI: 10.7270/Q2833SZB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50267086
PNG
(Adociaquinone B | CHEMBL476648)
Show SMILES C[C@@]12CCCc3coc(c13)C(=O)c1cc3C(=O)C4=NCCS(=O)(=O)C4C(=O)c3cc21 |r,t:19|
Show InChI InChI=1S/C22H17NO6S/c1-22-4-2-3-10-9-29-20(15(10)22)18(25)13-7-11-12(8-14(13)22)19(26)21-16(17(11)24)23-5-6-30(21,27)28/h7-9,21H,2-6H2,1H3/t21?,22-/m0/s1
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n/an/a 70n/an/an/an/an/an/a



Universit£ di Napoli Federico II

Curated by ChEMBL


Assay Description
Inhibition of Cdc25B


J Med Chem 55: 4142-58 (2012)


Article DOI: 10.1021/jm201624h
BindingDB Entry DOI: 10.7270/Q2X34ZJ9
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50267086
PNG
(Adociaquinone B | CHEMBL476648)
Show SMILES C[C@@]12CCCc3coc(c13)C(=O)c1cc3C(=O)C4=NCCS(=O)(=O)C4C(=O)c3cc21 |r,t:19|
Show InChI InChI=1S/C22H17NO6S/c1-22-4-2-3-10-9-29-20(15(10)22)18(25)13-7-11-12(8-14(13)22)19(26)21-16(17(11)24)23-5-6-30(21,27)28/h7-9,21H,2-6H2,1H3/t21?,22-/m0/s1
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n/an/a 80n/an/an/an/an/an/a



Virginia Polytechnic Institute and State University

Curated by ChEMBL


Assay Description
Inhibition of histidine-tagged full length human Cdc25B expressed in Escherichia coli


Bioorg Med Chem 17: 2276-81 (2009)


Article DOI: 10.1016/j.bmc.2008.10.090
BindingDB Entry DOI: 10.7270/Q21J99MN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM41999
PNG
(3-(3,4,5-trihydroxy-6-keto-xanthen-9-yl)propionic ...)
Show SMILES OC(=O)CCc1c2ccc(O)c(O)c2oc2c(O)c(=O)ccc12
Show InChI InChI=1S/C16H12O7/c17-10-4-1-8-7(3-6-12(19)20)9-2-5-11(18)14(22)16(9)23-15(8)13(10)21/h1-2,4-5,17,21-22H,3,6H2,(H,19,20)
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n/an/a 100n/an/an/an/an/an/a



Universit£ di Napoli Federico II

Curated by ChEMBL


Assay Description
Inhibition of recombinant phosphatase activity of Cdc25B catalytic domain expressed in Escherichia coli BL21(DE3) using OMFP as substrate by spectrof...


J Med Chem 55: 4142-58 (2012)


Article DOI: 10.1021/jm201624h
BindingDB Entry DOI: 10.7270/Q2X34ZJ9
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50208827
PNG
(2,3-bis(2-hydroxyethylthio)naphthalene-1,4-dione |...)
Show SMILES OCCSC1=C(SCCO)C(=O)c2ccccc2C1=O |c:4|
Show InChI InChI=1S/C14H14O4S2/c15-5-7-19-13-11(17)9-3-1-2-4-10(9)12(18)14(13)20-8-6-16/h1-4,15-16H,5-8H2
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n/an/a 100n/an/an/an/an/an/a



Sejong University

Curated by ChEMBL


Assay Description
Inhibition of GST tagged Cdc25B


Bioorg Med Chem Lett 17: 2351-4 (2007)


Article DOI: 10.1016/j.bmcl.2006.12.046
BindingDB Entry DOI: 10.7270/Q2DF6QWF
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50267086
PNG
(Adociaquinone B | CHEMBL476648)
Show SMILES C[C@@]12CCCc3coc(c13)C(=O)c1cc3C(=O)C4=NCCS(=O)(=O)C4C(=O)c3cc21 |r,t:19|
Show InChI InChI=1S/C22H17NO6S/c1-22-4-2-3-10-9-29-20(15(10)22)18(25)13-7-11-12(8-14(13)22)19(26)21-16(17(11)24)23-5-6-30(21,27)28/h7-9,21H,2-6H2,1H3/t21?,22-/m0/s1
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n/an/a 110n/an/an/an/an/an/a



Virginia Polytechnic Institute and State University

Curated by ChEMBL


Assay Description
Inhibition of histidine-tagged human recombinant Cdc25B catalytic domain expressed in Escherichia coli


Bioorg Med Chem 17: 2276-81 (2009)


Article DOI: 10.1016/j.bmc.2008.10.090
BindingDB Entry DOI: 10.7270/Q21J99MN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317356
PNG
(3-(3-stearoyl-1H-pyrazole-5-carboxamido)thiophene-...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1cc([nH]n1)C(=O)Nc1ccsc1C(O)=O
Show InChI InChI=1S/C27H41N3O4S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-24(31)22-20-23(30-29-22)26(32)28-21-18-19-35-25(21)27(33)34/h18-20H,2-17H2,1H3,(H,28,32)(H,29,30)(H,33,34)
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n/an/a 120n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50177318
PNG
(2-(4-(7-(4-tetradecylbenzoyl)cyclopenta[d][1,2]oxa...)
Show SMILES CCCCCCCCCCCCCCc1ccc(cc1)C(=O)c1ccc2c(nocc12)-c1ccc(OCC(O)=O)cc1
Show InChI InChI=1S/C36H43NO5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-27-15-17-29(18-16-27)36(40)32-24-23-31-33(32)25-42-37-35(31)28-19-21-30(22-20-28)41-26-34(38)39/h15-25H,2-14,26H2,1H3,(H,38,39)
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n/an/a 120n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
Inhibitory activity against cdc25B phosphatase


Bioorg Med Chem Lett 16: 499-502 (2005)


Article DOI: 10.1016/j.bmcl.2005.10.062
BindingDB Entry DOI: 10.7270/Q2319VFG
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50208827
PNG
(2,3-bis(2-hydroxyethylthio)naphthalene-1,4-dione |...)
Show SMILES OCCSC1=C(SCCO)C(=O)c2ccccc2C1=O |c:4|
Show InChI InChI=1S/C14H14O4S2/c15-5-7-19-13-11(17)9-3-1-2-4-10(9)12(18)14(13)20-8-6-16/h1-4,15-16H,5-8H2
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n/an/a 125n/an/an/an/an/an/a



Max-Planck-Institute of Molecular Physiology

Curated by ChEMBL


Assay Description
Inhibition of human Cdc25B


Bioorg Med Chem 19: 2145-55 (2011)


Article DOI: 10.1016/j.bmc.2011.02.047
BindingDB Entry DOI: 10.7270/Q2BR8SHK
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317355
PNG
(2-(3-stearoyl-1H-pyrazole-5-carboxamido)benzoic ac...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1cc([nH]n1)C(=O)Nc1ccccc1C(O)=O
Show InChI InChI=1S/C29H43N3O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-27(33)25-22-26(32-31-25)28(34)30-24-20-18-17-19-23(24)29(35)36/h17-20,22H,2-16,21H2,1H3,(H,30,34)(H,31,32)(H,35,36)
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n/an/a 160n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317365
PNG
(5-(4-chlorophenyl)-3-stearoylpyrrolo[3,4-c]pyrazol...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccc(Cl)cc1
Show InChI InChI=1S/C29H40ClN3O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-24(34)26-25-27(32-31-26)29(36)33(28(25)35)23-20-18-22(30)19-21-23/h18-21H,2-17H2,1H3,(H,31,32)
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n/an/a 170n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM124256
PNG
((3S,3aR,4S,7aS)-4-acetyl-7-dodecyl-3-methyl-1-oxo-...)
Show SMILES CCCCCCCCCCCCC\C=C\[C@]12[C@H]([C@H](C)OC1=O)[C@H](C(C)=O)C(=CC2CCCCCCCCCCCC)C(O)=O |r,c:27|
Show InChI InChI=1S/C39H66O5/c1-5-7-9-11-13-15-17-18-19-21-23-25-27-29-39-33(28-26-24-22-20-16-14-12-10-8-6-2)30-34(37(41)42)35(31(3)40)36(39)32(4)44-38(39)43/h27,29-30,32-33,35-36H,5-26,28H2,1-4H3,(H,41,42)/b29-27+/t32-,33?,35+,36+,39-/m0/s1
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n/an/a 200n/an/an/an/an/an/a



Lanzhou University





Org Biomol Chem 12: 3441-5 (2014)


Article DOI: 10.1039/c4ob00214h
BindingDB Entry DOI: 10.7270/Q2JQ0ZPC
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50297586
PNG
(CHEMBL557129 | N-(1-benzyl-3-cyano-1H-pyrrolo[3,2-...)
Show SMILES O=S(=O)(Nc1c(C#N)c2nc3ccccc3nc2n1Cc1ccccc1)c1ccccc1
Show InChI InChI=1S/C24H17N5O2S/c25-15-19-22-24(27-21-14-8-7-13-20(21)26-22)29(16-17-9-3-1-4-10-17)23(19)28-32(30,31)18-11-5-2-6-12-18/h1-14,28H,16H2
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n/an/a 200n/an/an/an/an/an/a



Sejong University

Curated by ChEMBL


Assay Description
Inhibition of GST-fused Cdc25B


Bioorg Med Chem Lett 19: 4372-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.05.078
BindingDB Entry DOI: 10.7270/Q2D79BGK
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50391109
PNG
(CHEMBL179166 | Sodium orthovanadate (SOV) | Vanada...)
Show SMILES [O-][V]([O-])([O-])=O
Show InChI InChI=1S/4O.V/q;3*-1;
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n/an/a 210n/an/an/an/an/an/a



Yanbian University College of Pharmacy

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GST-tagged CDC25B expressed in Escherichia coli BL21 (DE3) using pNPP as substrate measured for 2 mins by colorimetri...


Eur J Med Chem 172: 163-173 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.059
BindingDB Entry DOI: 10.7270/Q2028VWB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50106497
PNG
(6-Chloro-7-(2-morpholin-4-yl-ethylamino)-quinoline...)
Show SMILES Oc1c(Cl)c(N=CCN2CCOCC2)c(O)c2ncccc12 |w:6.6|
Show InChI InChI=1S/C15H16ClN3O3/c16-11-13(18-4-5-19-6-8-22-9-7-19)15(21)12-10(14(11)20)2-1-3-17-12/h1-4,20-21H,5-9H2
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n/an/a 210n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibitory activity against recombinant human cell division cycle 25B


J Med Chem 44: 4042-9 (2001)


BindingDB Entry DOI: 10.7270/Q2X34WR5
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50297585
PNG
(CHEMBL557673 | N-(1-benzyl-1H-pyrrolo[3,2-b]quinox...)
Show SMILES O=S(=O)(Nc1cc2nc3ccccc3nc2n1Cc1ccccc1)c1ccccc1
Show InChI InChI=1S/C23H18N4O2S/c28-30(29,18-11-5-2-6-12-18)26-22-15-21-23(25-20-14-8-7-13-19(20)24-21)27(22)16-17-9-3-1-4-10-17/h1-15,26H,16H2
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n/an/a 210n/an/an/an/an/an/a



Sejong University

Curated by ChEMBL


Assay Description
Inhibition of GST-fused Cdc25B


Bioorg Med Chem Lett 19: 4372-5 (2009)


Article DOI: 10.1016/j.bmcl.2009.05.078
BindingDB Entry DOI: 10.7270/Q2D79BGK
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM124255
PNG
((3S,3aR,4S,7R,7aS)-4-acetyl-7-dodecyl-3-methyl-1-o...)
Show SMILES CCCCCCCCCCCCC\C=C\[C@]12[C@H]([C@H](C)OC1=O)[C@H](C(C)=O)C(=C[C@H]2CCCCCCCCCCCC)C(O)=O |r,c:27|
Show InChI InChI=1S/C39H66O5/c1-5-7-9-11-13-15-17-18-19-21-23-25-27-29-39-33(28-26-24-22-20-16-14-12-10-8-6-2)30-34(37(41)42)35(31(3)40)36(39)32(4)44-38(39)43/h27,29-30,32-33,35-36H,5-26,28H2,1-4H3,(H,41,42)/b29-27+/t32-,33+,35+,36+,39-/m0/s1
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n/an/a 220n/an/an/an/an/an/a



Lanzhou University





Org Biomol Chem 12: 3441-5 (2014)


Article DOI: 10.1039/c4ob00214h
BindingDB Entry DOI: 10.7270/Q2JQ0ZPC
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM31040
PNG
(1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4...)
Show SMILES CCn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccccc1
Show InChI InChI=1S/C14H13N5O2/c1-3-19-12-10(13(20)18(2)14(21)16-12)15-11(17-19)9-7-5-4-6-8-9/h4-8H,3H2,1-2H3
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n/an/a 223n/an/an/an/an/an/a



University of Pittsburgh Molecular Library Screening Center

Curated by PubChem BioAssay


Assay Description
The Cdc25B Phosphatase Secondary Selectivity Assay has been developed and run at the University of Pittsburgh Molecular Screening Center (PMLSC) part...


PubChem Bioassay (2006)


BindingDB Entry DOI: 10.7270/Q2FF3QRT
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317352
PNG
(5-phenyl-3-stearoylpyrrolo[3,4-c]pyrazole-4,6(1H,5...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccccc1
Show InChI InChI=1S/C29H41N3O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-24(33)26-25-27(31-30-26)29(35)32(28(25)34)23-20-17-16-18-21-23/h16-18,20-21H,2-15,19,22H2,1H3,(H,30,31)
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n/an/a 230n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317364
PNG
(5-(3-chlorophenyl)-3-stearoylpyrrolo[3,4-c]pyrazol...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1cccc(Cl)c1
Show InChI InChI=1S/C29H40ClN3O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-20-24(34)26-25-27(32-31-26)29(36)33(28(25)35)23-19-17-18-22(30)21-23/h17-19,21H,2-16,20H2,1H3,(H,31,32)
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n/an/a 240n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317366
PNG
(5-(2-bromophenyl)-3-stearoylpyrrolo[3,4-c]pyrazole...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccccc1Br
Show InChI InChI=1S/C29H40BrN3O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-24(34)26-25-27(32-31-26)29(36)33(28(25)35)23-20-18-17-19-22(23)30/h17-20H,2-16,21H2,1H3,(H,31,32)
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n/an/a 250n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50504361
PNG
(CHEMBL4452484)
Show SMILES CSC1=C(SC)C(=O)c2ccccc2C1=O |c:2|
Show InChI InChI=1S/C12H10O2S2/c1-15-11-9(13)7-5-3-4-6-8(7)10(14)12(11)16-2/h3-6H,1-2H3
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n/an/a 250n/an/an/an/an/an/a



Montana State University

Curated by ChEMBL


Assay Description
Inhibition of recombinant Cdc25B (unknown origin) using OMFP as substrate measured every 30 sec for 10 mins by fluorometric assay


Eur J Med Chem 183: (2019)


Article DOI: 10.1016/j.ejmech.2019.111719
BindingDB Entry DOI: 10.7270/Q2D221X9
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50504361
PNG
(CHEMBL4452484)
Show SMILES CSC1=C(SC)C(=O)c2ccccc2C1=O |c:2|
Show InChI InChI=1S/C12H10O2S2/c1-15-11-9(13)7-5-3-4-6-8(7)10(14)12(11)16-2/h3-6H,1-2H3
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n/an/a 250n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50341995
PNG
(5-(2-(dimethylamino)ethylamino)-2,6-dimethylbenzo[...)
Show SMILES CN(C)CC=Nc1c(C)c(O)c2sc(C)nc2c1O |w:5.5|
Show InChI InChI=1S/C13H17N3O2S/c1-7-9(14-5-6-16(3)4)12(18)10-13(11(7)17)19-8(2)15-10/h5,17-18H,6H2,1-4H3
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n/an/a 250n/an/an/an/an/an/a



Max-Planck-Institute of Molecular Physiology

Curated by ChEMBL


Assay Description
Inhibition of human Cdc25B


Bioorg Med Chem 19: 2145-55 (2011)


Article DOI: 10.1016/j.bmc.2011.02.047
BindingDB Entry DOI: 10.7270/Q2BR8SHK
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50099736
PNG
(4-Ethoxy-[1,2]naphthoquinone | 4-ethoxynaphthalene...)
Show SMILES CCOC1=CC(=O)C(=O)c2ccccc12 |t:3|
Show InChI InChI=1S/C12H10O3/c1-2-15-11-7-10(13)12(14)9-6-4-3-5-8(9)11/h3-7H,2H2,1H3
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n/an/a 270n/an/an/an/an/an/a



Virginia Polytechnic Institute and State University

Curated by ChEMBL


Assay Description
Inhibition of histidine-tagged human recombinant Cdc25B catalytic domain expressed in Escherichia coli


Bioorg Med Chem 17: 2276-81 (2009)


Article DOI: 10.1016/j.bmc.2008.10.090
BindingDB Entry DOI: 10.7270/Q21J99MN
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50106505
PNG
(6-Chloro-7-(indan-1-ylamino)-quinoline-5,8-dione |...)
Show SMILES ClC1=C(NC2CCc3ccccc23)C(=O)c2ncccc2C1=O |c:1|
Show InChI InChI=1S/C18H13ClN2O2/c19-14-16(18(23)15-12(17(14)22)6-3-9-20-15)21-13-8-7-10-4-1-2-5-11(10)13/h1-6,9,13,21H,7-8H2
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n/an/a 300n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibitory activity against recombinant human cell division cycle 25B


J Med Chem 44: 4042-9 (2001)


BindingDB Entry DOI: 10.7270/Q2X34WR5
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317382
PNG
(5-(naphthalen-1-yl)-3-stearoylpyrrolo[3,4-c]pyrazo...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1cccc2ccccc12
Show InChI InChI=1S/C33H43N3O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-24-28(37)30-29-31(35-34-30)33(39)36(32(29)38)27-23-19-21-25-20-17-18-22-26(25)27/h17-23H,2-16,24H2,1H3,(H,34,35)
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n/an/a 310n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317376
PNG
(3-stearoyl-5-(2-(trifluoromethyl)phenyl)pyrrolo[3,...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccccc1C(F)(F)F
Show InChI InChI=1S/C30H40F3N3O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-24(37)26-25-27(35-34-26)29(39)36(28(25)38)23-20-18-17-19-22(23)30(31,32)33/h17-20H,2-16,21H2,1H3,(H,34,35)
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n/an/a 320n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50512278
PNG
(CHEMBL4475724)
Show SMILES OC(=O)C(Cc1c[nH]c2ccccc12)N1C(=S)S\C(=C/c2ccc3cc(OCc4ccc(Br)cc4)ccc3c2)C1=O
Show InChI InChI=1S/C32H23BrN2O4S2/c33-24-10-6-19(7-11-24)18-39-25-12-9-21-13-20(5-8-22(21)15-25)14-29-30(36)35(32(40)41-29)28(31(37)38)16-23-17-34-27-4-2-1-3-26(23)27/h1-15,17,28,34H,16,18H2,(H,37,38)/b29-14-
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n/an/a 320n/an/an/an/an/an/a



Yanbian University College of Pharmacy

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GST-tagged CDC25B expressed in Escherichia coli BL21 (DE3) using pNPP as substrate measured for 2 mins by colorimetri...


Eur J Med Chem 172: 163-173 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.059
BindingDB Entry DOI: 10.7270/Q2028VWB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317380
PNG
(CHEMBL1098821 | methyl 3-(4,6-dioxo-3-stearoylpyrr...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccsc1C(=O)OC
Show InChI InChI=1S/C29H41N3O5S/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-22(33)24-23-25(31-30-24)28(35)32(27(23)34)21-19-20-38-26(21)29(36)37-2/h19-20H,3-18H2,1-2H3,(H,30,31)
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n/an/a 340n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM32102
PNG
(1,6-dimethylpyrimido[5,4-e][1,2,4]triazine-5,7(1H,...)
Show SMILES Cn1ncnc2c1nc(=O)n(C)c2=O
Show InChI InChI=1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3
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n/an/a 349n/an/an/an/an/an/a



University of Pittsburgh Molecular Library Screening Center

Curated by PubChem BioAssay


Assay Description
The Cdc25B Phosphatase HTS dose response confirmation has been developed to confirm actives identified in the Cdc25B HTS AID 368, screened at the Uni...


PubChem Bioassay (2006)


BindingDB Entry DOI: 10.7270/Q2BG2MCP
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50106491
PNG
(5-Amino-6-(7-amino-6-methoxy-5,8-dioxo-5,8-dihydro...)
Show SMILES COC1C(=N)C(=O)c2nc(ccc2C1=O)-c1nc(C(=O)OC)c(C)c(c1N)-c1ccc(OC)c(OC)c1O |(10.32,-.31,;10.33,-1.86,;11.68,-2.63,;11.68,-4.17,;10.33,-4.94,;13,-4.93,;13.01,-6.48,;14.33,-4.16,;15.67,-4.93,;17,-4.16,;16.98,-2.62,;15.65,-1.86,;14.33,-2.63,;13,-1.85,;13,-.29,;18.33,-4.93,;19.66,-4.15,;21,-4.92,;22.33,-4.15,;22.31,-2.6,;23.67,-4.91,;25,-4.12,;21,-6.46,;22.34,-7.23,;19.66,-7.25,;18.33,-6.48,;17,-7.25,;19.67,-8.79,;18.33,-9.55,;18.33,-11.09,;19.66,-11.86,;19.67,-13.41,;18.33,-14.18,;21,-11.09,;22.34,-11.85,;22.35,-13.4,;21,-9.55,;22.33,-8.78,)|
Show InChI InChI=1S/C26H24N4O8/c1-10-15(11-7-9-14(35-2)24(36-3)21(11)31)16(27)20(30-18(10)26(34)38-5)13-8-6-12-19(29-13)23(33)17(28)25(37-4)22(12)32/h6-9,25,28,31H,27H2,1-5H3
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University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibitory activity against recombinant human cell division cycle 25B


J Med Chem 44: 4042-9 (2001)


BindingDB Entry DOI: 10.7270/Q2X34WR5
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50512277
PNG
(CHEMBL4445615)
Show SMILES OC(=O)C(Cc1c[nH]c2ccccc12)N1C(=S)S\C(=C/c2ccc3cc(OCc4ccc(F)cc4)ccc3c2)C1=O
Show InChI InChI=1S/C32H23FN2O4S2/c33-24-10-6-19(7-11-24)18-39-25-12-9-21-13-20(5-8-22(21)15-25)14-29-30(36)35(32(40)41-29)28(31(37)38)16-23-17-34-27-4-2-1-3-26(23)27/h1-15,17,28,34H,16,18H2,(H,37,38)/b29-14-
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n/an/a 380n/an/an/an/an/an/a



Yanbian University College of Pharmacy

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GST-tagged CDC25B expressed in Escherichia coli BL21 (DE3) using pNPP as substrate measured for 2 mins by colorimetri...


Eur J Med Chem 172: 163-173 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.059
BindingDB Entry DOI: 10.7270/Q2028VWB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM32102
PNG
(1,6-dimethylpyrimido[5,4-e][1,2,4]triazine-5,7(1H,...)
Show SMILES Cn1ncnc2c1nc(=O)n(C)c2=O
Show InChI InChI=1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3
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n/an/a 396n/an/an/an/an/an/a



University of Pittsburgh Molecular Library Screening Center

Curated by PubChem BioAssay


Assay Description
The MKP-1 Dual Specificity Protein Tyrosine Phosphatase Probe Assessment Cdc25B Dose Response Selectivity Assay has been developed to evaluate the PT...


PubChem Bioassay (2007)


BindingDB Entry DOI: 10.7270/Q2125R2H
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50033731
PNG
((R)-5,8-dihydroxy-2-(1-hydroxy-4-methylpent-3-enyl...)
Show SMILES CC(C)C=CC(=O)c1cc(O)c2c(O)ccc(O)c2c1O |w:4.4|
Show InChI InChI=1S/C16H16O5/c1-8(2)3-4-10(17)9-7-13(20)14-11(18)5-6-12(19)15(14)16(9)21/h3-8,18-21H,1-2H3
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n/an/a 400n/an/an/an/an/an/a



Montana State University

Curated by ChEMBL


Assay Description
Inhibition of recombinant Cdc25B (unknown origin) using OMFP as substrate measured every 30 sec for 10 mins by fluorometric assay


Eur J Med Chem 183: (2019)


Article DOI: 10.1016/j.ejmech.2019.111719
BindingDB Entry DOI: 10.7270/Q2D221X9
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50261252
PNG
(CHEMBL511236 | [((R)-4-Hexadecanoyl-3-hydroxy-5-ox...)
Show SMILES CCCCCCCCCCCCCCCC(=O)C1C(=O)O[C@H](COC(=O)N=C=NC(=O)OCC)C1=O |r|
Show InChI InChI=1S/C26H40N2O8/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-20(29)22-23(30)21(36-24(22)31)18-35-26(33)28-19-27-25(32)34-4-2/h21-22H,3-18H2,1-2H3/t21-,22?/m1/s1
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University of Bayreuth

Curated by ChEMBL


Assay Description
Inhibition of cdc25B


Bioorg Med Chem 16: 4203-21 (2008)


Article DOI: 10.1016/j.bmc.2008.02.069
BindingDB Entry DOI: 10.7270/Q2C24W6P
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM31040
PNG
(1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4...)
Show SMILES CCn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccccc1
Show InChI InChI=1S/C14H13N5O2/c1-3-19-12-10(13(20)18(2)14(21)16-12)15-11(17-19)9-7-5-4-6-8-9/h4-8H,3H2,1-2H3
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n/an/a 400n/an/an/an/an/an/a



University of Pittsburgh Molecular Library Screening Center

Curated by PubChem BioAssay


Assay Description
The Cdc25B Phosphatase HTS dose response confirmation has been developed to confirm actives identified in the Cdc25B HTS AID 368, screened at the Uni...


PubChem Bioassay (2006)


BindingDB Entry DOI: 10.7270/Q2BG2MCP
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317359
PNG
(5-(4-nitrophenyl)-3-stearoylpyrrolo[3,4-c]pyrazole...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C29H40N4O5/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-24(34)26-25-27(31-30-26)29(36)32(28(25)35)22-18-20-23(21-19-22)33(37)38/h18-21H,2-17H2,1H3,(H,30,31)
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n/an/a 400n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317374
PNG
(CHEMBL1098791 | methyl 2-(4,6-dioxo-3-stearoylpyrr...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccccc1C(=O)OC
Show InChI InChI=1S/C31H43N3O5/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-22-25(35)27-26-28(33-32-27)30(37)34(29(26)36)24-21-19-18-20-23(24)31(38)39-2/h18-21H,3-17,22H2,1-2H3,(H,32,33)
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n/an/a 410n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM31044
PNG
(1-Ethyl-6-methyl-3-thiophen-2-yl-1H-pyrimido[5,4-e...)
Show SMILES CCn1nc(nc2c1nc(=O)n(C)c2=O)-c1cccs1
Show InChI InChI=1S/C12H11N5O2S/c1-3-17-10-8(11(18)16(2)12(19)14-10)13-9(15-17)7-5-4-6-20-7/h4-6H,3H2,1-2H3
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n/an/a 421n/an/an/an/an/an/a



University of Pittsburgh Molecular Library Screening Center

Curated by PubChem BioAssay


Assay Description
The Cdc25B Phosphatase probe assessment dose response reproducibility assay has been developed to re-confirm actives that were identified in the Cdc2...


PubChem Bioassay (2007)


BindingDB Entry DOI: 10.7270/Q25T3HWF
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50106503
PNG
(6-Chloro-7-(2-morpholin-4-yl-ethylamino)-phthalazi...)
Show SMILES Oc1c(Cl)c(N=CCN2CCOCC2)c(O)c2cnncc12 |w:6.6|
Show InChI InChI=1S/C14H15ClN4O3/c15-11-12(16-1-2-19-3-5-22-6-4-19)14(21)10-8-18-17-7-9(10)13(11)20/h1,7-8,20-21H,2-6H2
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n/an/a 430n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibitory activity against recombinant human cell division cycle 25B


J Med Chem 44: 4042-9 (2001)


BindingDB Entry DOI: 10.7270/Q2X34WR5
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM31040
PNG
(1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4...)
Show SMILES CCn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccccc1
Show InChI InChI=1S/C14H13N5O2/c1-3-19-12-10(13(20)18(2)14(21)16-12)15-11(17-19)9-7-5-4-6-8-9/h4-8H,3H2,1-2H3
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n/an/a 447n/an/an/an/an/an/a



University of Pittsburgh Molecular Library Screening Center

Curated by PubChem BioAssay


Assay Description
The MKP-1 Dual Specificity Protein Tyrosine Phosphatase Probe Assessment Cdc25B Dose Response Selectivity Assay has been developed to evaluate the PT...


PubChem Bioassay (2007)


BindingDB Entry DOI: 10.7270/Q2125R2H
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50106493
PNG
(7-[2-(4-Hydroxy-3-methoxy-phenyl)-ethylamino]-quin...)
Show SMILES COc1cc(CC=Nc2cc(O)c3cccnc3c2O)ccc1O |w:6.5|
Show InChI InChI=1S/C18H16N2O4/c1-24-16-9-11(4-5-14(16)21)6-8-19-13-10-15(22)12-3-2-7-20-17(12)18(13)23/h2-5,7-10,21-23H,6H2,1H3
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n/an/a 450n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibitory activity against recombinant human cell division cycle 25B


J Med Chem 44: 4042-9 (2001)


BindingDB Entry DOI: 10.7270/Q2X34WR5
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317361
PNG
(5-(2-fluorophenyl)-3-stearoylpyrrolo[3,4-c]pyrazol...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccccc1F
Show InChI InChI=1S/C29H40FN3O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-24(34)26-25-27(32-31-26)29(36)33(28(25)35)23-20-18-17-19-22(23)30/h17-20H,2-16,21H2,1H3,(H,31,32)
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n/an/a 450n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50512272
PNG
(CHEMBL4450252)
Show SMILES OC(=O)C(Cc1c[nH]c2ccccc12)N1C(=S)S\C(=C/c2ccc3cc(OCc4ccc(Cl)cc4Cl)ccc3c2)C1=O
Show InChI InChI=1S/C32H22Cl2N2O4S2/c33-23-9-7-21(26(34)15-23)17-40-24-10-8-19-11-18(5-6-20(19)13-24)12-29-30(37)36(32(41)42-29)28(31(38)39)14-22-16-35-27-4-2-1-3-25(22)27/h1-13,15-16,28,35H,14,17H2,(H,38,39)/b29-12-
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n/an/a 490n/an/an/an/an/an/a



Yanbian University College of Pharmacy

Curated by ChEMBL


Assay Description
Inhibition of human recombinant GST-tagged CDC25B expressed in Escherichia coli BL21 (DE3) using pNPP as substrate measured for 2 mins by colorimetri...


Eur J Med Chem 172: 163-173 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.059
BindingDB Entry DOI: 10.7270/Q2028VWB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317375
PNG
(CHEMBL1098792 | methyl 4-(4,6-dioxo-3-stearoylpyrr...)
Show SMILES CCCCCCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccc(cc1)C(=O)OC
Show InChI InChI=1S/C31H43N3O5/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-25(35)27-26-28(33-32-27)30(37)34(29(26)36)24-21-19-23(20-22-24)31(38)39-2/h19-22H,3-18H2,1-2H3,(H,32,33)
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n/an/a 490n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM31040
PNG
(1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4...)
Show SMILES CCn1nc(nc2c1nc(=O)n(C)c2=O)-c1ccccc1
Show InChI InChI=1S/C14H13N5O2/c1-3-19-12-10(13(20)18(2)14(21)16-12)15-11(17-19)9-7-5-4-6-8-9/h4-8H,3H2,1-2H3
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n/an/a 493n/an/an/an/an/an/a



University of Pittsburgh Molecular Library Screening Center

Curated by PubChem BioAssay


Assay Description
The Cdc25B Phosphatase probe assessment dose response reproducibility assay has been developed to re-confirm actives that were identified in the Cdc2...


PubChem Bioassay (2007)


BindingDB Entry DOI: 10.7270/Q25T3HWF
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50317358
PNG
(5-(4-nitrophenyl)-3-tetradecanoylpyrrolo[3,4-c]pyr...)
Show SMILES CCCCCCCCCCCCCC(=O)c1n[nH]c2C(=O)N(C(=O)c12)c1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C25H32N4O5/c1-2-3-4-5-6-7-8-9-10-11-12-13-20(30)22-21-23(27-26-22)25(32)28(24(21)31)18-14-16-19(17-15-18)29(33)34/h14-17H,2-13H2,1H3,(H,26,27)
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n/an/a 500n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of CDC25B


Bioorg Med Chem Lett 20: 2876-9 (2010)


Article DOI: 10.1016/j.bmcl.2010.03.040
BindingDB Entry DOI: 10.7270/Q2W959CB
More data for this
Ligand-Target Pair
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