Found 28 hits with Last Name = 'prévost' and Initial = 'g' 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 3
(Homo sapiens (Human)) | BDBM50175215
(6-(2-(dimethylamino)ethylamino)-2-ethylbenzo[d]oxa...)Show InChI InChI=1S/C13H17N3O3/c1-4-10-15-11-9(17)7-8(12(18)13(11)19-10)14-5-6-16(2)3/h5,7,17-18H,4,6H2,1-3H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175216
(5-(2-(dimethylamino)ethylamino)-2-ethylbenzo[d]oxa...)Show InChI InChI=1S/C13H17N3O3/c1-4-10-15-11-12(18)8(14-5-6-16(2)3)7-9(17)13(11)19-10/h5,7,17-18H,4,6H2,1-3H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175218
(5-(2-(dimethylamino)ethylamino)-2-methylbenzo[d]th...)Show InChI InChI=1S/C12H15N3O2S/c1-7-14-10-11(17)8(13-4-5-15(2)3)6-9(16)12(10)18-7/h4,6,16-17H,5H2,1-3H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175219
(6-(2-(dimethylamino)ethylamino)-2-phenylbenzo[d]ox...)Show SMILES CN(C)CC=Nc1cc(O)c2nc(oc2c1O)-c1ccccc1 |w:5.5| Show InChI InChI=1S/C17H17N3O3/c1-20(2)9-8-18-12-10-13(21)14-16(15(12)22)23-17(19-14)11-6-4-3-5-7-11/h3-8,10,21-22H,9H2,1-2H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
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 |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175217
(5-(2-(dimethylamino)ethylamino)-2-phenylbenzo[d]ox...)Show SMILES CN(C)CC=Nc1cc(O)c2oc(nc2c1O)-c1ccccc1 |w:5.5| Show InChI InChI=1S/C17H17N3O3/c1-20(2)9-8-18-12-10-13(21)16-14(15(12)22)19-17(23-16)11-6-4-3-5-7-11/h3-8,10,21-22H,9H2,1-2H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
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 |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(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
KEGG
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| 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 |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155597
(4-Dimethylamino-2-{[2-(4-nitro-phenyl)-ethylamino]...)Show SMILES CN(C)c1ccc(O)c(CNCCc2ccc(cc2)[N+]([O-])=O)c1 Show InChI InChI=1S/C17H21N3O3/c1-19(2)16-7-8-17(21)14(11-16)12-18-10-9-13-3-5-15(6-4-13)20(22)23/h3-8,11,18,21H,9-10,12H2,1-2H3 | PDB
MMDB
KEGG
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AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 3.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155595
(4-Dimethylamino-2-methoxy-6-{[2-(4-nitro-phenyl)-e...)Show SMILES COc1cc(cc(CNCCc2ccc(cc2)[N+]([O-])=O)c1O)N(C)C Show InChI InChI=1S/C18H23N3O4/c1-20(2)16-10-14(18(22)17(11-16)25-3)12-19-9-8-13-4-6-15(7-5-13)21(23)24/h4-7,10-11,19,22H,8-9,12H2,1-3H3 | PDB
MMDB
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AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50370437
(BN-82002 | CHEMBL1258871)Show SMILES COc1cc(cc(CN(C)CCc2ccc(cc2)[N+]([O-])=O)c1C)N(C)C Show InChI InChI=1S/C20H27N3O3/c1-15-17(12-19(21(2)3)13-20(15)26-5)14-22(4)11-10-16-6-8-18(9-7-16)23(24)25/h6-9,12-13H,10-11,14H2,1-5H3 | PDB
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B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155599
(4-Dimethylamino-2-({methyl-[2-(4-nitro-phenyl)-eth...)Show SMILES CN(C)c1ccc(O)c(CN(C)CCc2ccc(cc2)[N+]([O-])=O)c1 Show InChI InChI=1S/C18H23N3O3/c1-19(2)17-8-9-18(22)15(12-17)13-20(3)11-10-14-4-6-16(7-5-14)21(23)24/h4-9,12,22H,10-11,13H2,1-3H3 | PDB
MMDB
KEGG
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B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 5.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175220
(5-(2-(dimethylamino)ethylamino)-2-ethyl-1H-benzo[d...)Show SMILES CCc1nc2c(O)cc(N=CCN(C)C)c(O)c2[nH]1 |w:9.8| Show InChI InChI=1S/C13H18N4O2/c1-4-10-15-11-9(18)7-8(13(19)12(11)16-10)14-5-6-17(2)3/h5,7,18-19H,4,6H2,1-3H3,(H,15,16) | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175222
(6-(2-(dimethylamino)ethylamino)-2-phenyl-2H-indazo...)Show SMILES CN(C)CC=Nc1cc(O)c2cn(nc2c1O)-c1ccccc1 |w:5.5| Show InChI InChI=1S/C17H18N4O2/c1-20(2)9-8-18-14-10-15(22)13-11-21(19-16(13)17(14)23)12-6-4-3-5-7-12/h3-8,10-11,22-23H,9H2,1-2H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175223
(5-(2-(dimethylamino)ethylamino)-2-phenyl-2H-indazo...)Show SMILES CN(C)CC=Nc1cc(O)c2nn(cc2c1O)-c1ccccc1 |w:5.5| Show InChI InChI=1S/C17H18N4O2/c1-20(2)9-8-18-14-10-15(22)16-13(17(14)23)11-21(19-16)12-6-4-3-5-7-12/h3-8,10-11,22-23H,9H2,1-2H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175221
(5-(2-(dimethylamino)ethylamino)-2-phenyl-1H-benzo[...)Show SMILES CN(C)CC=Nc1cc(O)c2nc([nH]c2c1O)-c1ccccc1 |w:5.5| Show InChI InChI=1S/C17H18N4O2/c1-21(2)9-8-18-12-10-13(22)14-15(16(12)23)20-17(19-14)11-6-4-3-5-7-11/h3-8,10,22-23H,9H2,1-2H3,(H,19,20) | PDB
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PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM24778
(2-methyl-1,4-dihydronaphthalene-1,4-dione | 2-meth...)Show InChI InChI=1S/C11H8O2/c1-7-6-10(12)8-4-2-3-5-9(8)11(7)13/h2-6H,1H3 | PDB
MMDB
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MCE
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PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.88E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM24778
(2-methyl-1,4-dihydronaphthalene-1,4-dione | 2-meth...)Show InChI InChI=1S/C11H8O2/c1-7-6-10(12)8-4-2-3-5-9(8)11(7)13/h2-6H,1H3 | PDB
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PC cid
PC sid
PDB
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Patents
Similars
| Article
PubMed
| n/a | n/a | 1.90E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155594
(2-Dimethylamino-6-methoxy-4-({methyl-[2-(4-nitro-p...)Show SMILES COc1cc(CN(C)CCc2ccc(cc2)[N+]([O-])=O)cc(N(C)C)c1O Show InChI InChI=1S/C19H25N3O4/c1-20(2)17-11-15(12-18(26-4)19(17)23)13-21(3)10-9-14-5-7-16(8-6-14)22(24)25/h5-8,11-12,23H,9-10,13H2,1-4H3 | PDB
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PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.07E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155596
(CHEMBL187753 | Dimethyl-[3-({methyl-[2-(4-nitro-ph...)Show SMILES CN(C)c1cccc(CN(C)CCc2ccc(cc2)[N+]([O-])=O)c1 Show InChI InChI=1S/C18H23N3O2/c1-19(2)18-6-4-5-16(13-18)14-20(3)12-11-15-7-9-17(10-8-15)21(22)23/h4-10,13H,11-12,14H2,1-3H3 | PDB
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PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155598
((3-Methoxy-benzyl)-methyl-[2-(4-nitro-phenyl)-ethy...)Show InChI InChI=1S/C17H20N2O3/c1-18(13-15-4-3-5-17(12-15)22-2)11-10-14-6-8-16(9-7-14)19(20)21/h3-9,12H,10-11,13H2,1-2H3 | PDB
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KEGG
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155593
(2-Methoxy-6-({methyl-[2-(4-nitro-phenyl)-ethyl]-am...)Show InChI InChI=1S/C17H20N2O4/c1-18(12-14-4-3-5-16(23-2)17(14)20)11-10-13-6-8-15(9-7-13)19(21)22/h3-9,20H,10-12H2,1-2H3 | PDB
MMDB
KEGG
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B.MOAD
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155592
(2-({Methyl-[2-(4-nitro-phenyl)-ethyl]-amino}-methy...)Show SMILES CN(CCc1ccc(cc1)[N+]([O-])=O)Cc1cc(ccc1O)[N+]([O-])=O Show InChI InChI=1S/C16H17N3O5/c1-17(9-8-12-2-4-14(5-3-12)18(21)22)11-13-10-15(19(23)24)6-7-16(13)20/h2-7,10,20H,8-9,11H2,1H3 | PDB
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| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155590
((2,3-Dimethoxy-benzyl)-methyl-[2-(4-nitro-phenyl)-...)Show SMILES COc1cccc(CN(C)CCc2ccc(cc2)[N+]([O-])=O)c1OC Show InChI InChI=1S/C18H22N2O4/c1-19(12-11-14-7-9-16(10-8-14)20(21)22)13-15-5-4-6-17(23-2)18(15)24-3/h4-10H,11-13H2,1-3H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155602
(CHEMBL359780 | [3-Methoxy-4-({methyl-[2-(4-nitro-p...)Show SMILES COc1cc(ccc1CN(C)CCc1ccc(cc1)[N+]([O-])=O)N(C)C Show InChI InChI=1S/C19H25N3O3/c1-20(2)18-10-7-16(19(13-18)25-4)14-21(3)12-11-15-5-8-17(9-6-15)22(23)24/h5-10,13H,11-12,14H2,1-4H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155588
(Benzyl-methyl-[2-(4-nitro-phenyl)-ethyl]-amine | C...)Show InChI InChI=1S/C16H18N2O2/c1-17(13-15-5-3-2-4-6-15)12-11-14-7-9-16(10-8-14)18(19)20/h2-10H,11-13H2,1H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155589
(CHEMBL185815 | Dimethyl-[4-({methyl-[2-(4-nitro-ph...)Show SMILES CN(C)c1ccc(CN(C)CCc2ccc(cc2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C18H23N3O2/c1-19(2)17-8-6-16(7-9-17)14-20(3)13-12-15-4-10-18(11-5-15)21(22)23/h4-11H,12-14H2,1-3H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155600
(2-({Methyl-[2-(4-nitro-phenyl)-ethyl]-amino}-methy...)Show InChI InChI=1S/C16H18N2O3/c1-17(12-14-4-2-3-5-16(14)19)11-10-13-6-8-15(9-7-13)18(20)21/h2-9,19H,10-12H2,1H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50155601
((2,5-Dimethoxy-benzyl)-methyl-[2-(4-nitro-phenyl)-...)Show SMILES COc1ccc(OC)c(CN(C)CCc2ccc(cc2)[N+]([O-])=O)c1 Show InChI InChI=1S/C18H22N2O4/c1-19(11-10-14-4-6-16(7-5-14)20(21)22)13-15-12-17(23-2)8-9-18(15)24-3/h4-9,12H,10-11,13H2,1-3H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >8.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory concentration for human cell division cycle 25 degree C phosphatase; not active |
Bioorg Med Chem Lett 14: 5809-12 (2004)
Article DOI: 10.1016/j.bmcl.2004.09.041
BindingDB Entry DOI: 10.7270/Q2H41S67 |
More data for this
Ligand-Target Pair | |
M-phase inducer phosphatase 3
(Homo sapiens (Human)) | BDBM50175224
(5-(2-(dimethylamino)ethylamino)-2-methyl-2H-isoind...)Show InChI InChI=1S/C13H17N3O2/c1-15(2)5-4-14-11-6-12(17)9-7-16(3)8-10(9)13(11)18/h4,6-8,17-18H,5H2,1-3H3 | PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 8.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description
Inhibitory activity against recombinant CDC25C |
Bioorg Med Chem Lett 16: 171-5 (2005)
Article DOI: 10.1016/j.bmcl.2005.09.030
BindingDB Entry DOI: 10.7270/Q2T1535S |
More data for this
Ligand-Target Pair | |
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