Compile Data Set for Download or QSAR
Report error Found 46 Enz. Inhib. hit(s) with all data for entry = 50040946
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402647BDBM50402647(CHEMBL2206732)
Affinity DataIC50: 1.38E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 24778BDBM24778(Vitamin K3 | cid_4055 | 2-methyl-1,4-dihydronaphth...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402654BDBM50402654(CHEMBL2207337)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402665BDBM50402665(CHEMBL2206740)
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402650BDBM50402650(CHEMBL2206756)
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402653BDBM50402653(CHEMBL2206734)
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402664BDBM50402664(CHEMBL2206741)
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402660BDBM50402660(CHEMBL2206745)
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402647BDBM50402647(CHEMBL2206732)
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 10 mM dithio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402647BDBM50402647(CHEMBL2206732)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 20 mM dithio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402648BDBM50402648(CHEMBL2206754)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402658BDBM50402658(CHEMBL2206753)
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402657BDBM50402657(CHEMBL2206755)
Affinity DataIC50: 3.90E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402663BDBM50402663(CHEMBL2206742)
Affinity DataIC50: 4.40E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402650BDBM50402650(CHEMBL2206756)
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402656BDBM50402656(CHEMBL2207335)
Affinity DataIC50: 6.60E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402655BDBM50402655(CHEMBL2207336)
Affinity DataIC50: 7.50E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402666BDBM50402666(CHEMBL2206739)
Affinity DataIC50: 7.70E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402659BDBM50402659(CHEMBL2206751)
Affinity DataIC50: 8.40E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402661BDBM50402661(CHEMBL2206744)
Affinity DataIC50: 8.50E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402656BDBM50402656(CHEMBL2207335)
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402655BDBM50402655(CHEMBL2207336)
Affinity DataIC50: 9.10E+3nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402668BDBM50402668(CHEMBL2206731)
Affinity DataIC50: 1.12E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402657BDBM50402657(CHEMBL2206755)
Affinity DataIC50: 1.16E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402649BDBM50402649(CHEMBL2206736)
Affinity DataIC50: 1.19E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetDual specificity protein phosphatase 3(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402649BDBM50402649(CHEMBL2206736)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of VHR using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402658BDBM50402658(CHEMBL2206753)
Affinity DataIC50: 1.24E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402667BDBM50402667(CHEMBL2206737)
Affinity DataIC50: 1.38E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402651BDBM50402651(CHEMBL2206752)
Affinity DataIC50: 1.39E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402648BDBM50402648(CHEMBL2206754)
Affinity DataIC50: 1.65E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 10 mM dithio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402648BDBM50402648(CHEMBL2206754)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 20 mM dithio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402651BDBM50402651(CHEMBL2206752)
Affinity DataIC50: 2.06E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402669BDBM50402669(CHEMBL2206730)
Affinity DataIC50: 2.06E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402652BDBM50402652(CHEMBL2206735)
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402653BDBM50402653(CHEMBL2206734)
Affinity DataIC50: 2.34E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402647BDBM50402647(CHEMBL2206732)
Affinity DataIC50: 2.42E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402649BDBM50402649(CHEMBL2206736)
Affinity DataIC50: 2.69E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402659BDBM50402659(CHEMBL2206751)
Affinity DataIC50: 2.84E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402648BDBM50402648(CHEMBL2206754)
Affinity DataIC50: 3.06E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetDual specificity protein phosphatase 3(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402650BDBM50402650(CHEMBL2206756)
Affinity DataIC50: 3.31E+4nMAssay Description:Inhibition of VHR using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402670BDBM50402670(CHEMBL2206729)
Affinity DataIC50: 4.01E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402652BDBM50402652(CHEMBL2206735)
Affinity DataIC50: 4.13E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402654BDBM50402654(CHEMBL2207337)
Affinity DataIC50: 4.60E+4nMAssay Description:Inhibition of PTP1B using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402671BDBM50402671(CHEMBL2206728)
Affinity DataIC50: 4.84E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402662BDBM50402662(CHEMBL2206743)
Affinity DataIC50: 5.73E+4nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetDual specificity protein phosphatase 3(Human)
University of Paris

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50402651BDBM50402651(CHEMBL2206752)
Affinity DataIC50: 7.58E+4nMAssay Description:Inhibition of VHR using fluorescein 3,6 diphosphate as substrate measured for 1 hr in presence of 1 mM dithiothreitolMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed