Compile Data Set for Download or QSAR
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Found 12 of ic50 for monomerid = 82577
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50:  3.70E+3nMAssay Description:Inhibition of recombinant VHR (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50:  3.71E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetReceptor-type tyrosine-protein phosphatase R(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of recombinant PTP-SL (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 22(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50:  2.60E+4nMAssay Description:Inhibition of recombinant VHX (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 7(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50:  3.80E+4nMAssay Description:Inhibition of recombinant HePTP (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 22(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50:  4.90E+4nMAssay Description:Inhibition of recombinant LYP (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50:  5.50E+4nMAssay Description:Inhibition of recombinant TCPTP (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase F(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant LAR (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 5(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant STEP (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant PTP1B (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 6(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant MKP3 (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein phosphatase C(Homo sapiens (Human))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM82577((4-fluoro-1,3-benzothiazol-2-yl)-[5-(4-methoxyphen...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant CD45 (unknown origin) using OMFP as substrate after 1 hr by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed