Found 97 hits Enz. Inhib. hit(s) with Target = 'Dual specificity protein phosphatase 2' AND taxid = 9606 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 |
|---|
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM199180
(US9217012, 10)Show SMILES CCc1ccc(cc1)C(=O)NCCCCC(NC(=O)C(Cc1ccc(cc1)C(F)(F)P(O)(O)=O)NC(=O)C(Cc1ccccc1)NC(=O)COC1CC(C)CCC1C(C)C)C(N)=O Show InChI InChI=1S/C46H62F2N5O9P/c1-5-31-15-19-34(20-16-31)43(56)50-24-10-9-13-37(42(49)55)52-45(58)39(27-33-17-21-35(22-18-33)46(47,48)63(59,60)61)53-44(57)38(26-32-11-7-6-8-12-32)51-41(54)28-62-40-25-30(4)14-23-36(40)29(2)3/h6-8,11-12,15-22,29-30,36-40H,5,9-10,13-14,23-28H2,1-4H3,(H2,49,55)(H,50,56)(H,51,54)(H,52,58)(H,53,57)(H2,59,60,61) | PDB
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| PC cid
PC sid
UniChem
| US Patent
| >1.00E+3 | >-34.2 | n/a | n/a | n/a | n/a | n/a | 7.0 | 25 |
Indiana University Research and Technology Corporation
US Patent
| Assay Description
PTP activity was assayed using p-nitrophenyl phosphate (pNPP) as a substrate in DMG buffer (50 mM DMG, pH 7.0, 1 mM EDTA, 150 mM NaCl, 2 mM DTT, 0.1 ... |
US Patent US9217012 (2015)
BindingDB Entry DOI: 10.7270/Q2FX788H |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168874
(3-{5-[1-(4-Fluoro-phenyl)-meth-(Z)-ylidene]-4-oxo-...)Show SMILES OC(=O)c1cccc(c1)N1C(=S)S\C(=C/c2ccc(F)cc2)C1=O Show InChI InChI=1S/C17H10FNO3S2/c18-12-6-4-10(5-7-12)8-14-15(20)19(17(23)24-14)13-3-1-2-11(9-13)16(21)22/h1-9H,(H,21,22)/b14-8- | PDB
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| Article
PubMed
| n/a | n/a | 1.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50425807
(CHEMBL2316902)Show SMILES OC(=O)c1cc2c(C#Cc3cccc(c3)C(F)(F)F)c(oc2cc1O)-c1ccccc1 Show InChI InChI=1S/C24H13F3O4/c25-24(26,27)16-8-4-5-14(11-16)9-10-17-18-12-19(23(29)30)20(28)13-21(18)31-22(17)15-6-2-1-3-7-15/h1-8,11-13,28H,(H,29,30) | PDB
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| Article
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| n/a | n/a | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Indiana University School of Medicine
Curated by ChEMBL
| Assay Description
Inhibition of VHX (unknown origin) expressed in Escherichia coli using pNPP substrate after 5 mins by spectrophotometric analysis |
J Med Chem 56: 832-42 (2013)
Article DOI: 10.1021/jm301781p
BindingDB Entry DOI: 10.7270/Q2KK9D4X |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50425806
(CHEMBL2316907)Show SMILES OC(=O)c1cc2c(C#Cc3ccc(OC(F)(F)F)cc3)c(oc2cc1O)-c1ccccc1 Show InChI InChI=1S/C24H13F3O5/c25-24(26,27)32-16-9-6-14(7-10-16)8-11-17-18-12-19(23(29)30)20(28)13-21(18)31-22(17)15-4-2-1-3-5-15/h1-7,9-10,12-13,28H,(H,29,30) | PDB
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| n/a | n/a | 1.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Indiana University School of Medicine
Curated by ChEMBL
| Assay Description
Inhibition of VHX (unknown origin) expressed in Escherichia coli using pNPP substrate after 5 mins by spectrophotometric analysis |
J Med Chem 56: 832-42 (2013)
Article DOI: 10.1021/jm301781p
BindingDB Entry DOI: 10.7270/Q2KK9D4X |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50556732
(CHEMBL4750435)Show SMILES COc1ccc(cc1)-n1cc(-c2ccc3ccc(=O)oc3c2)c2cc(cnc12)-c1ccc(cc1)C(O)=O | PDB
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| Article
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| n/a | n/a | 2.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of DUSP22 (unknown origin) pre-incubated for 20 mins followed by fluorescence substrate addition and measured after 120 mins by DiFMUP ass... |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.0c01265
BindingDB Entry DOI: 10.7270/Q24171QP |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205422
(CHEMBL230941 | N3-cyclohexyl-N1-(2,3-di(furan-2-yl...)Show SMILES O=C(NC1CCCCC1)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:9.9| Show InChI InChI=1S/C29H31N5O4/c35-28(30-20-8-2-1-3-9-20)19-7-4-14-34(18-19)29(36)31-21-12-13-22-23(17-21)33-27(25-11-6-16-38-25)26(32-22)24-10-5-15-37-24/h5-6,10-13,15-17,19-20H,1-4,7-9,14,18H2,(H,30,35)(H,31,36) | PDB
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| n/a | n/a | 2.25E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 23
(Homo sapiens (Human)) | BDBM50054344
(CHEMBL3319356 | US9522881, 11a-1 L97M74 | US984453...)Show SMILES Cn1c(c(I)c2cc(C(O)=O)c(O)cc12)-c1cccc(NC(=O)C(=O)Nc2ccc(cc2)-c2ccsc2)c1 Show InChI InChI=1S/C28H20IN3O5S/c1-32-22-13-23(33)21(28(36)37)12-20(22)24(29)25(32)16-3-2-4-19(11-16)31-27(35)26(34)30-18-7-5-15(6-8-18)17-9-10-38-14-17/h2-14,33H,1H3,(H,30,34)(H,31,35)(H,36,37) | PDB
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| US Patent
| n/a | n/a | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Indiana University Research and Technology Corporation
US Patent
| Assay Description
For selectivity studies, the PTPs, including LYP, mPTPA, SHP1-D1C, PTP1B, LMPTP, VHR, Laforin and PTPα-D1D2 were expressed and purified from E. ... |
US Patent US9522881 (2016)
BindingDB Entry DOI: 10.7270/Q2DN4402 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 23
(Homo sapiens (Human)) | BDBM50054344
(CHEMBL3319356 | US9522881, 11a-1 L97M74 | US984453...)Show SMILES Cn1c(c(I)c2cc(C(O)=O)c(O)cc12)-c1cccc(NC(=O)C(=O)Nc2ccc(cc2)-c2ccsc2)c1 Show InChI InChI=1S/C28H20IN3O5S/c1-32-22-13-23(33)21(28(36)37)12-20(22)24(29)25(32)16-3-2-4-19(11-16)31-27(35)26(34)30-18-7-5-15(6-8-18)17-9-10-38-14-17/h2-14,33H,1H3,(H,30,34)(H,31,35)(H,36,37) | PDB
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| n/a | n/a | 2.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Indiana University School of Medicine
Curated by ChEMBL
| Assay Description
Inhibition of VHZ (unknown origin) |
J Med Chem 57: 6594-609 (2014)
Article DOI: 10.1021/jm5006176
BindingDB Entry DOI: 10.7270/Q24X59FM |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205419
(CHEMBL230472 | N3-butyl-N1-(2,3-di(furan-2-yl)quin...)Show SMILES CCCCN(CC)C(=O)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:9.8| Show InChI InChI=1S/C29H33N5O4/c1-3-5-14-33(4-2)28(35)20-9-6-15-34(19-20)29(36)30-21-12-13-22-23(18-21)32-27(25-11-8-17-38-25)26(31-22)24-10-7-16-37-24/h7-8,10-13,16-18,20H,3-6,9,14-15,19H2,1-2H3,(H,30,36) | PDB
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| n/a | n/a | 2.35E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205439
(CHEMBL230576 | N1-(2,3-di(furan-2-yl)quinoxalin-6-...)Show SMILES CCCN(CCC)C(=O)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:9.8| Show InChI InChI=1S/C29H33N5O4/c1-3-13-33(14-4-2)28(35)20-8-5-15-34(19-20)29(36)30-21-11-12-22-23(18-21)32-27(25-10-7-17-38-25)26(31-22)24-9-6-16-37-24/h6-7,9-12,16-18,20H,3-5,8,13-15,19H2,1-2H3,(H,30,36) | PDB
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| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168885
(3-{5-[1-(4-Nitro-phenyl)-meth-(Z)-ylidene]-4-oxo-2...)Show SMILES OC(=O)c1cccc(c1)-n1c([O-])c([CH+]c2ccc(cc2)[N+]([O-])=O)sc1=S Show InChI InChI=1S/C17H10N2O5S2/c20-15-14(8-10-4-6-12(7-5-10)19(23)24)26-17(25)18(15)13-3-1-2-11(9-13)16(21)22/h1-9H,(H-,20,21,22) | PDB
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| n/a | n/a | 2.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205438
(CHEMBL396800 | N3-butyl-N1-(2,3-di(furan-2-yl)quin...)Show SMILES CCCCNC(=O)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:7.6| Show InChI InChI=1S/C27H29N5O4/c1-2-3-12-28-26(33)18-7-4-13-32(17-18)27(34)29-19-10-11-20-21(16-19)31-25(23-9-6-15-36-23)24(30-20)22-8-5-14-35-22/h5-6,8-11,14-16,18H,2-4,7,12-13,17H2,1H3,(H,28,33)(H,29,34) | PDB
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| n/a | n/a | 2.79E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50425808
(CHEMBL2316906)Show SMILES OC(=O)c1cc2c(C#Cc3cc(F)cc(F)c3)c(oc2cc1O)-c1ccccc1 Show InChI InChI=1S/C23H12F2O4/c24-15-8-13(9-16(25)10-15)6-7-17-18-11-19(23(27)28)20(26)12-21(18)29-22(17)14-4-2-1-3-5-14/h1-5,8-12,26H,(H,27,28) | PDB
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| n/a | n/a | 2.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Indiana University School of Medicine
Curated by ChEMBL
| Assay Description
Inhibition of VHX (unknown origin) expressed in Escherichia coli using pNPP substrate after 5 mins by spectrophotometric analysis |
J Med Chem 56: 832-42 (2013)
Article DOI: 10.1021/jm301781p
BindingDB Entry DOI: 10.7270/Q2KK9D4X |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205426
(CHEMBL230843 | N3-cyclopentyl-N1-(2,3-di(furan-2-y...)Show SMILES O=C(NC1CCCC1)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:8.8| Show InChI InChI=1S/C28H29N5O4/c34-27(29-19-7-1-2-8-19)18-6-3-13-33(17-18)28(35)30-20-11-12-21-22(16-20)32-26(24-10-5-15-37-24)25(31-21)23-9-4-14-36-23/h4-5,9-12,14-16,18-19H,1-3,6-8,13,17H2,(H,29,34)(H,30,35) | PDB
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| n/a | n/a | 3.02E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 23
(Homo sapiens (Human)) | BDBM50436358
(CHEMBL2396718)Show SMILES CCCNC(=O)COc1ccc(cc1)-c1oc2cc(O)c(cc2c1C#Cc1cccc(Cl)c1)C(O)=O Show InChI InChI=1S/C28H22ClNO6/c1-2-12-30-26(32)16-35-20-9-7-18(8-10-20)27-21(11-6-17-4-3-5-19(29)13-17)22-14-23(28(33)34)24(31)15-25(22)36-27/h3-5,7-10,13-15,31H,2,12,16H2,1H3,(H,30,32)(H,33,34) | PDB
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| n/a | n/a | 3.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Indiana University School of Medicine
Curated by ChEMBL
| Assay Description
Inhibition of recombinant VHZ (unknown origin) using pNPP as substrate by spectrophotometric analysis |
J Med Chem 56: 4990-5008 (2013)
Article DOI: 10.1021/jm400248c
BindingDB Entry DOI: 10.7270/Q2N017XW |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168896
(4-{5-[1-(4-Fluoro-phenyl)-meth-(Z)-ylidene]-4-oxo-...)Show SMILES OC(=O)c1ccc(cc1)N1C(=S)S\C(=C/c2ccc(F)cc2)C1=O Show InChI InChI=1S/C17H10FNO3S2/c18-12-5-1-10(2-6-12)9-14-15(20)19(17(23)24-14)13-7-3-11(4-8-13)16(21)22/h1-9H,(H,21,22)/b14-9- | PDB
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| n/a | n/a | 4.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205428
(CHEMBL230471 | N3-butyl-N1-(2,3-di(furan-2-yl)quin...)Show SMILES CCCCN(C)C(=O)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:8.7| Show InChI InChI=1S/C28H31N5O4/c1-3-4-13-32(2)27(34)19-8-5-14-33(18-19)28(35)29-20-11-12-21-22(17-20)31-26(24-10-7-16-37-24)25(30-21)23-9-6-15-36-23/h6-7,9-12,15-17,19H,3-5,8,13-14,18H2,1-2H3,(H,29,35) | PDB
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| n/a | n/a | 5.55E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 23
(Homo sapiens (Human)) | BDBM50436357
(CHEMBL2396719)Show SMILES OC(=O)c1cc2c(C#Cc3cccc(Cl)c3)c(oc2cc1O)-c1ccc(OCC(=O)NC2CC2)cc1 Show InChI InChI=1S/C28H20ClNO6/c29-18-3-1-2-16(12-18)4-11-21-22-13-23(28(33)34)24(31)14-25(22)36-27(21)17-5-9-20(10-6-17)35-15-26(32)30-19-7-8-19/h1-3,5-6,9-10,12-14,19,31H,7-8,15H2,(H,30,32)(H,33,34) | PDB
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| n/a | n/a | 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Indiana University School of Medicine
Curated by ChEMBL
| Assay Description
Inhibition of recombinant VHZ (unknown origin) using pNPP as substrate by spectrophotometric analysis |
J Med Chem 56: 4990-5008 (2013)
Article DOI: 10.1021/jm400248c
BindingDB Entry DOI: 10.7270/Q2N017XW |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168876
(3-{4-Oxo-5-[1-phenyl-meth-(Z)-ylidene]-2-thioxo-th...)Show SMILES OC(=O)c1cccc(c1)N1C(=S)S\C(=C/c2ccccc2)C1=O Show InChI InChI=1S/C17H11NO3S2/c19-15-14(9-11-5-2-1-3-6-11)23-17(22)18(15)13-8-4-7-12(10-13)16(20)21/h1-10H,(H,20,21)/b14-9- | PDB
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| n/a | n/a | 7.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168876
(3-{4-Oxo-5-[1-phenyl-meth-(Z)-ylidene]-2-thioxo-th...)Show SMILES OC(=O)c1cccc(c1)N1C(=S)S\C(=C/c2ccccc2)C1=O Show InChI InChI=1S/C17H11NO3S2/c19-15-14(9-11-5-2-1-3-6-11)23-17(22)18(15)13-8-4-7-12(10-13)16(20)21/h1-10H,(H,20,21)/b14-9- | PDB
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| n/a | n/a | 7.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168893
(3-{5-[1-Cyclohexyl-meth-(Z)-ylidene]-4-oxo-2-thiox...)Show SMILES OC(=O)c1cccc(c1)N1C(=S)S\C(=C/C2CCCCC2)C1=O Show InChI InChI=1S/C17H17NO3S2/c19-15-14(9-11-5-2-1-3-6-11)23-17(22)18(15)13-8-4-7-12(10-13)16(20)21/h4,7-11H,1-3,5-6H2,(H,20,21)/b14-9- | PDB
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| n/a | n/a | 7.30E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205429
(CHEMBL425838 | N3-tert-butyl-N1-(2,3-di(furan-2-yl...)Show SMILES CC(C)(C)NC(=O)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:7.6| Show InChI InChI=1S/C27H29N5O4/c1-27(2,3)31-25(33)17-7-4-12-32(16-17)26(34)28-18-10-11-19-20(15-18)30-24(22-9-6-14-36-22)23(29-19)21-8-5-13-35-21/h5-6,8-11,13-15,17H,4,7,12,16H2,1-3H3,(H,28,34)(H,31,33) | PDB
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| n/a | n/a | 8.05E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205427
(CHEMBL230681 | N1-(2,3-di(furan-2-yl)quinoxalin-6-...)Show SMILES CC(C)CNC(=O)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:7.6| Show InChI InChI=1S/C27H29N5O4/c1-17(2)15-28-26(33)18-6-3-11-32(16-18)27(34)29-19-9-10-20-21(14-19)31-25(23-8-5-13-36-23)24(30-20)22-7-4-12-35-22/h4-5,7-10,12-14,17-18H,3,6,11,15-16H2,1-2H3,(H,28,33)(H,29,34) | PDB
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| n/a | n/a | 8.36E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205432
(CHEMBL446453 | N-(2,3-di(furan-2-yl)quinoxalin-6-y...)Show SMILES O=C(Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1)N1CCCC(C1)C(=O)N1CCCCC1 |w:27.33| Show InChI InChI=1S/C28H29N5O4/c34-27(32-12-2-1-3-13-32)19-7-4-14-33(18-19)28(35)29-20-10-11-21-22(17-20)31-26(24-9-6-16-37-24)25(30-21)23-8-5-15-36-23/h5-6,8-11,15-17,19H,1-4,7,12-14,18H2,(H,29,35) | PDB
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| n/a | n/a | 8.39E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488935
(CHEMBL2299386)Show SMILES OC(=O)c1cc(ccc1Cl)-c1ccc(\C=C2/C=C(OC2=O)c2ccc(Cl)cc2)o1 |c:17| Show InChI InChI=1S/C22H12Cl2O5/c23-15-4-1-12(2-5-15)20-11-14(22(27)29-20)9-16-6-8-19(28-16)13-3-7-18(24)17(10-13)21(25)26/h1-11H,(H,25,26)/b14-9+ | PDB
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| n/a | n/a | 8.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 2
(Homo sapiens (Human)) | BDBM50360601
(CHEMBL1933349 | MK-0893)Show SMILES COc1ccc2cc(ccc2c1)-c1cc(nn1[C@@H](C)c1ccc(cc1)C(=O)NCCC(O)=O)-c1cc(Cl)cc(Cl)c1 |r| Show InChI InChI=1S/C32H27Cl2N3O4/c1-19(20-3-5-21(6-4-20)32(40)35-12-11-31(38)39)37-30(18-29(36-37)25-14-26(33)17-27(34)15-25)24-8-7-23-16-28(41-2)10-9-22(23)13-24/h3-10,13-19H,11-12H2,1-2H3,(H,35,40)(H,38,39)/t19-/m0/s1 | PDB
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| n/a | n/a | 9.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories
Curated by ChEMBL
| Assay Description
Antagonist activity at human PAC1 expressed in mouse HIN 3T3 cells assessed as inhibition of glucagon-induced cAMP accumulation preincubated for 30 m... |
J Med Chem 55: 6137-48 (2012)
Article DOI: 10.1021/jm300579z
BindingDB Entry DOI: 10.7270/Q2X63P2C |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168894
((4-{4-Oxo-5-[1-phenyl-meth-(Z)-ylidene]-2-thioxo-t...)Show SMILES OP(O)(=O)Cc1ccc(cc1)N1C(=S)SC(=Cc2ccccc2)C1=O |w:16.17| Show InChI InChI=1S/C17H14NO4PS2/c19-16-15(10-12-4-2-1-3-5-12)25-17(24)18(16)14-8-6-13(7-9-14)11-23(20,21)22/h1-10H,11H2,(H2,20,21,22) | PDB
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| n/a | n/a | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 23
(Homo sapiens (Human)) | BDBM50607111
(CHEMBL5218807) | PDB
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| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| |
Citation and Details
Article DOI: 10.1021/acs.jmedchem.2c01143
BindingDB Entry DOI: 10.7270/Q2BK1HGF |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM231167
(US9340574, 7)Show SMILES COc1cc(CC(=O)NCC(NC(=O)C(CCCNC(=O)c2cccc(I)c2)NC(=O)C(Cc2ccc(cc2)C(F)(F)P(O)(O)=O)NC(=O)c2ccc(C)c(Br)c2)C(N)=O)ccc1O Show InChI InChI=1S/C42H45BrF2IN6O11P/c1-23-8-12-27(21-30(23)43)39(57)51-32(17-24-9-13-28(14-10-24)42(44,45)64(60,61)62)41(59)50-31(7-4-16-48-38(56)26-5-3-6-29(46)20-26)40(58)52-33(37(47)55)22-49-36(54)19-25-11-15-34(53)35(18-25)63-2/h3,5-6,8-15,18,20-21,31-33,53H,4,7,16-17,19,22H2,1-2H3,(H2,47,55)(H,48,56)(H,49,54)(H,50,59)(H,51,57)(H,52,58)(H2,60,61,62) | PDB
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| US Patent
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | 7.0 | n/a |
Indiana University Research and Technology Corporation
US Patent
| Assay Description
PTP activity was assayed using p-nitrophenyl phosphate (pNPP) as a substrate in 3,3-dimethylglutarate buffer (50 mM 3,3-dimethylglutarate, pH 7.0, 1 ... |
US Patent US9340574 (2016)
BindingDB Entry DOI: 10.7270/Q2NV9H4J |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168886
(4-{4-Oxo-5-[1-phenyl-meth-(Z)-ylidene]-2-thioxo-th...)Show SMILES OS(=O)(=O)c1ccc(cc1)N1C(=S)S\C(=C/c2ccccc2)C1=O Show InChI InChI=1S/C16H11NO4S3/c18-15-14(10-11-4-2-1-3-5-11)23-16(22)17(15)12-6-8-13(9-7-12)24(19,20)21/h1-10H,(H,19,20,21)/b14-10- | PDB
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| n/a | n/a | 1.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 23
(Homo sapiens (Human)) | BDBM50087856
(CHEMBL3426913)Show SMILES CCCCC(Oc1cc(O)c(cc1C#Cc1ccccc1OC(F)(F)F)C(O)=O)C(=O)NC1CCCCC1 Show InChI InChI=1S/C28H30F3NO6/c1-2-3-12-24(26(34)32-20-10-5-4-6-11-20)37-25-17-22(33)21(27(35)36)16-19(25)15-14-18-9-7-8-13-23(18)38-28(29,30)31/h7-9,13,16-17,20,24,33H,2-6,10-12H2,1H3,(H,32,34)(H,35,36) | PDB
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| n/a | n/a | 1.14E+4 | n/a | n/a | n/a | n/a | 7.0 | n/a |
Indiana University
Curated by ChEMBL
| Assay Description
Inhibition of VHZ (unknown origin) using pNPP as substrate at pH 7 at 25 degC by spectrophotometric analysis |
Bioorg Med Chem 23: 2798-809 (2015)
Article DOI: 10.1016/j.bmc.2015.03.066
BindingDB Entry DOI: 10.7270/Q2VD7168 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50205425
(CHEMBL230842 | N1-(2,3-di(furan-2-yl)quinoxalin-6-...)Show SMILES CCN(CC)C(=O)C1CCCN(C1)C(=O)Nc1ccc2nc(-c3ccco3)c(nc2c1)-c1ccco1 |w:7.6| Show InChI InChI=1S/C27H29N5O4/c1-3-31(4-2)26(33)18-8-5-13-32(17-18)27(34)28-19-11-12-20-21(16-19)30-25(23-10-7-15-36-23)24(29-20)22-9-6-14-35-22/h6-7,9-12,14-16,18H,3-5,8,13,17H2,1-2H3,(H,28,34) | PDB
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| n/a | n/a | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description
Inhibition of GST-tagged human recombinant JSP1 |
Bioorg Med Chem Lett 17: 2118-22 (2007)
Article DOI: 10.1016/j.bmcl.2007.01.094
BindingDB Entry DOI: 10.7270/Q2R49QFR |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488945
(CHEMBL2299387)Show SMILES CN1C(=O)\C(S\C1=N\c1cccc(c1)C(O)=O)=C\c1ccc(OCc2cccc(F)c2)cc1 Show InChI InChI=1S/C25H19FN2O4S/c1-28-23(29)22(33-25(28)27-20-7-3-5-18(14-20)24(30)31)13-16-8-10-21(11-9-16)32-15-17-4-2-6-19(26)12-17/h2-14H,15H2,1H3,(H,30,31)/b22-13-,27-25+ | PDB
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| n/a | n/a | 1.25E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168877
(2-Hydroxy-5-{4-oxo-5-[1-phenyl-meth-(Z)-ylidene]-2...)Show SMILES OC(=O)c1cc(ccc1O)N1C(=S)S\C(=C/c2ccccc2)C1=O Show InChI InChI=1S/C17H11NO4S2/c19-13-7-6-11(9-12(13)16(21)22)18-15(20)14(24-17(18)23)8-10-4-2-1-3-5-10/h1-9,19H,(H,21,22)/b14-8- | PDB
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| n/a | n/a | 1.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168882
(2-Hydroxy-4-{4-oxo-5-[1-phenyl-meth-(Z)-ylidene]-2...)Show SMILES OC(=O)c1ccc(cc1O)N1C(=S)S\C(=C/c2ccccc2)C1=O Show InChI InChI=1S/C17H11NO4S2/c19-13-9-11(6-7-12(13)16(21)22)18-15(20)14(24-17(18)23)8-10-4-2-1-3-5-10/h1-9,19H,(H,21,22)/b14-8- | PDB
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| n/a | n/a | 1.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168875
(3-{4-Oxo-2-thioxo-5-[1-p-tolyl-meth-(Z)-ylidene]-t...)Show SMILES Cc1ccc(\C=C2/SC(=S)N(C2=O)c2cccc(c2)C(O)=O)cc1 Show InChI InChI=1S/C18H13NO3S2/c1-11-5-7-12(8-6-11)9-15-16(20)19(18(23)24-15)14-4-2-3-13(10-14)17(21)22/h2-10H,1H3,(H,21,22)/b15-9- | PDB
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| n/a | n/a | 1.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50087879
(CHEMBL472004 | NSC-87877)Show SMILES Oc1c(cc(c2cccnc12)S(O)(=O)=O)\N=N\c1ccc2cc(ccc2c1)S(O)(=O)=O Show InChI InChI=1S/C19H13N3O7S2/c23-19-16(10-17(31(27,28)29)15-2-1-7-20-18(15)19)22-21-13-5-3-12-9-14(30(24,25)26)6-4-11(12)8-13/h1-10,23H,(H,24,25,26)(H,27,28,29)/b22-21+ | PDB
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| n/a | n/a | 1.67E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of DUSP26 (unknown origin)-mediated p38 dephosphorylation |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488942
(CHEMBL2299388)Show SMILES OC(=O)c1ccc(Cl)cc1Nc1nc2ccccc2nc1NS(=O)(=O)c1ccc(Cl)cc1 Show InChI InChI=1S/C21H14Cl2N4O4S/c22-12-5-8-14(9-6-12)32(30,31)27-20-19(24-16-3-1-2-4-17(16)25-20)26-18-11-13(23)7-10-15(18)21(28)29/h1-11H,(H,24,26)(H,25,27)(H,28,29) | PDB
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| n/a | n/a | 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168881
(4-{4-Oxo-5-[1-phenyl-meth-(Z)-ylidene]-2-thioxo-th...)Show SMILES OC(=O)c1ccc(cc1)N1C(=S)S\C(=C/c2ccccc2)C1=O Show InChI InChI=1S/C17H11NO3S2/c19-15-14(10-11-4-2-1-3-5-11)23-17(22)18(15)13-8-6-12(7-9-13)16(20)21/h1-10H,(H,20,21)/b14-10- | PDB
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| n/a | n/a | 1.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488938
(CHEMBL2296000)Show SMILES CN1C(=O)\C(S\C1=N\c1cccc(c1)C(O)=O)=C\c1ccc(OCc2cccc(c2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C25H19N3O6S/c1-27-23(29)22(35-25(27)26-19-6-3-5-18(14-19)24(30)31)13-16-8-10-21(11-9-16)34-15-17-4-2-7-20(12-17)28(32)33/h2-14H,15H2,1H3,(H,30,31)/b22-13-,26-25+ | PDB
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| n/a | n/a | 1.98E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168883
((4-{4-Oxo-5-[1-phenyl-meth-(Z)-ylidene]-2-thioxo-t...)Show SMILES OC(=O)Cc1ccc(cc1)N1C(=S)S\C(=C/c2ccccc2)C1=O Show InChI InChI=1S/C18H13NO3S2/c20-16(21)11-13-6-8-14(9-7-13)19-17(22)15(24-18(19)23)10-12-4-2-1-3-5-12/h1-10H,11H2,(H,20,21)/b15-10- | PDB
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| n/a | n/a | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168878
((3-{4-Oxo-5-[1-phenyl-meth-(Z)-ylidene]-2-thioxo-t...)Show SMILES OC(=O)Cc1cccc(c1)N1C(=S)S\C(=C/c2ccccc2)C1=O Show InChI InChI=1S/C18H13NO3S2/c20-16(21)11-13-7-4-8-14(9-13)19-17(22)15(24-18(19)23)10-12-5-2-1-3-6-12/h1-10H,11H2,(H,20,21)/b15-10- | PDB
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| n/a | n/a | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488946
(CHEMBL2295992)Show SMILES OC(=O)CCN1C(=S)S\C(=C/c2cn(nc2-c2cccc(c2)[N+]([O-])=O)-c2ccccc2)C1=O Show InChI InChI=1S/C22H16N4O5S2/c27-19(28)9-10-24-21(29)18(33-22(24)32)12-15-13-25(16-6-2-1-3-7-16)23-20(15)14-5-4-8-17(11-14)26(30)31/h1-8,11-13H,9-10H2,(H,27,28)/b18-12- | PDB
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| n/a | n/a | 2.23E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488947
(CHEMBL2295993)Show SMILES OC(=O)c1cccc(c1)N1C(=S)S\C(=C\c2ccc(O)c(O)c2)C1=O Show InChI InChI=1S/C17H11NO5S2/c19-12-5-4-9(6-13(12)20)7-14-15(21)18(17(24)25-14)11-3-1-2-10(8-11)16(22)23/h1-8,19-20H,(H,22,23)/b14-7+ | PDB
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| n/a | n/a | 2.51E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM50168897
(3-{5-[1-(4-Methoxy-phenyl)-meth-(Z)-ylidene]-4-oxo...)Show SMILES COc1ccc(\C=C2/SC(=S)N(C2=O)c2cccc(c2)C(O)=O)cc1 Show InChI InChI=1S/C18H13NO4S2/c1-23-14-7-5-11(6-8-14)9-15-16(20)19(18(24)25-15)13-4-2-3-12(10-13)17(21)22/h2-10H,1H3,(H,21,22)/b15-9- | PDB
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| n/a | n/a | 2.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Ceptyr Inc.
Curated by ChEMBL
| Assay Description
Inhibition of JNK-stimulating phosphatase-1 (JSP-1) |
Bioorg Med Chem Lett 15: 3374-9 (2005)
Article DOI: 10.1016/j.bmcl.2005.05.034
BindingDB Entry DOI: 10.7270/Q2NG4Q4B |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 22
(Homo sapiens (Human)) | BDBM82577
((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)Show InChI InChI=1S/C16H11FN4O2S/c1-22-10-7-5-9(6-8-10)14-20-21-15(23-14)19-16-18-13-11(17)3-2-4-12(13)24-16/h2-8H,1H3,(H,18,19,21) | PDB
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| n/a | n/a | 2.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanford-Burnham Medical Research Institute
Curated by ChEMBL
| Assay Description
Inhibition of recombinant VHX (unknown origin) using OMFP as substrate after 1 hr by fluorescence assay |
Bioorg Med Chem 23: 2786-97 (2015)
Article DOI: 10.1016/j.bmc.2015.03.075
BindingDB Entry DOI: 10.7270/Q2BG2QQD |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488941
(CHEMBL2295994)Show SMILES OC(=O)c1cc(O)ccc1NC(=O)CN1C(=S)S\C(=C\C=C\c2ccccc2)C1=O Show InChI InChI=1S/C21H16N2O5S2/c24-14-9-10-16(15(11-14)20(27)28)22-18(25)12-23-19(26)17(30-21(23)29)8-4-7-13-5-2-1-3-6-13/h1-11,24H,12H2,(H,22,25)(H,27,28)/b7-4+,17-8+ | PDB
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| n/a | n/a | 2.63E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488937
(CHEMBL2296001)Show SMILES CN1C(=O)\C(S\C1=N\c1cccc(c1)C(O)=O)=C\c1ccc(OCc2ccc(F)cc2)cc1 Show InChI InChI=1S/C25H19FN2O4S/c1-28-23(29)22(33-25(28)27-20-4-2-3-18(14-20)24(30)31)13-16-7-11-21(12-8-16)32-15-17-5-9-19(26)10-6-17/h2-14H,15H2,1H3,(H,30,31)/b22-13-,27-25+ | PDB
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| n/a | n/a | 2.69E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488940
(CHEMBL2295995)Show SMILES OC(=O)c1cccc(c1)N1C(=S)S\C(=C/c2ccc(OCC=C)cc2)C1=O Show InChI InChI=1S/C20H15NO4S2/c1-2-10-25-16-8-6-13(7-9-16)11-17-18(22)21(20(26)27-17)15-5-3-4-14(12-15)19(23)24/h2-9,11-12H,1,10H2,(H,23,24)/b17-11- | PDB
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| n/a | n/a | 3.02E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
Dual specificity protein phosphatase 26
(Homo sapiens) | BDBM50488939
(CHEMBL2295996)Show SMILES CCc1cc(CC)cc(OCCOc2ccccc2\C=C2\C(=O)NN(C2=O)c2ccccc2)c1 Show InChI InChI=1S/C28H28N2O4/c1-3-20-16-21(4-2)18-24(17-20)33-14-15-34-26-13-9-8-10-22(26)19-25-27(31)29-30(28(25)32)23-11-6-5-7-12-23/h5-13,16-19H,3-4,14-15H2,1-2H3,(H,29,31)/b25-19- | PDB
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| n/a | n/a | 3.66E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
inhibition of Homo sapiens (human) recombinant DUSP26 catalytic domain (61 to 211 amino acid residues) overexpressed in Escherichia coli BL21 (DE3) a... |
Citation and Details
Article DOI: 10.1007/s00044-012-0405-3
BindingDB Entry DOI: 10.7270/Q2571FW0 |
More data for this
Ligand-Target Pair | |
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