Found 957 hits of ic50 data for polymerid = 6311 Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
M-phase inducer phosphatase 2
(Homo sapiens (Human)) | BDBM50612011
(CHEMBL5288122) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| UniChem
| | n/a | n/a | 53 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
|
More data for this Ligand-Target Pair | |
M-phase inducer phosphatase 2
(Homo sapiens (Human)) | BDBM50612010
(CHEMBL5271462) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| UniChem
| | n/a | n/a | 53 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
|
More data for this Ligand-Target Pair | |
M-phase inducer phosphatase 2
(Homo sapiens (Human)) | BDBM50267086
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 80 | n/a | n/a | n/a | n/a | n/a | n/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
(3-(3,4,5-trihydroxy-6-keto-xanthen-9-yl)propionic ...)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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/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
(2,3-bis(2-hydroxyethylthio)naphthalene-1,4-dione |...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/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
(2,3-bis(2-hydroxyethylthio)naphthalene-1,4-dione |...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 125 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 160 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/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
((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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/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
(CHEMBL179166 | Sodium orthovanadate (SOV) | Vanada...) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid PDB UniChem
Similars
| Article PubMed
| n/a | n/a | 210 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 210 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 210 | n/a | n/a | n/a | n/a | n/a | n/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
((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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 220 | n/a | n/a | n/a | n/a | n/a | n/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
(1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
Patents
Similars
| PCBioAssay
| n/a | n/a | 223 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 240 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/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
(CHEMBL4452484)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/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
(CHEMBL4452484)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
| | n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
|
More data for this Ligand-Target Pair | |
M-phase inducer phosphatase 2
(Homo sapiens (Human)) | BDBM50341995
(5-(2-(dimethylamino)ethylamino)-2,6-dimethylbenzo[...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 250 | n/a | n/a | n/a | n/a | n/a | n/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
(4-Ethoxy-[1,2]naphthoquinone | 4-ethoxynaphthalene...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 310 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 320 | n/a | n/a | n/a | n/a | n/a | n/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
(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- | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 320 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 340 | n/a | n/a | n/a | n/a | n/a | n/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
(1,6-dimethylpyrimido[5,4-e][1,2,4]triazine-5,7(1H,...)Show InChI InChI=1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
MCE KEGG PC cid PC sid PDB UniChem
Patents
Similars
| PCBioAssay
| n/a | n/a | 349 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 370 | n/a | n/a | n/a | n/a | n/a | n/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)) | BDBM50512277
(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- | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 380 | n/a | n/a | n/a | n/a | n/a | n/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
(1,6-dimethylpyrimido[5,4-e][1,2,4]triazine-5,7(1H,...)Show InChI InChI=1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
MCE KEGG PC cid PC sid PDB UniChem
Patents
Similars
| PCBioAssay
| n/a | n/a | 396 | n/a | n/a | n/a | n/a | n/a | n/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
((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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/a |
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
(1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
Patents
Similars
| PCBioAssay
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 410 | n/a | n/a | n/a | n/a | n/a | n/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
(1-Ethyl-6-methyl-3-thiophen-2-yl-1H-pyrimido[5,4-e...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
Similars
| PCBioAssay
| n/a | n/a | 421 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 430 | n/a | n/a | n/a | n/a | n/a | n/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
(1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
Patents
Similars
| PCBioAssay
| n/a | n/a | 447 | n/a | n/a | n/a | n/a | n/a | n/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
(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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | 450 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 450 | n/a | n/a | n/a | n/a | n/a | n/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
(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- | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 490 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 490 | n/a | n/a | n/a | n/a | n/a | n/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
(1-Ethyl-6-methyl-3-phenyl-1H-pyrimido[5,4-e][1,2,4...)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 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
Patents
Similars
| PCBioAssay
| n/a | n/a | 493 | n/a | n/a | n/a | n/a | n/a | n/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
(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) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 500 | n/a | n/a | n/a | n/a | n/a | n/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 | |