Compile Data Set for Download or QSAR
Found 61 Enz. Inhib. hit(s) with Target = 'Receptor-type tyrosine-protein phosphatase epsilon'
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118744(2-(Oxalyl-amino)-4,7-dihydro-5H-thieno[2,3-c]pyran...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118751(6-(Oxalyl-amino)-1H-indole-7-carboxylic acid | 6-(...)copy SMILEScopy InChI
Affinity DataKi:  3.30E+4nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118778(5-iodo-2-(oxaloamino)benzoic acid | CHEMBL336908)copy SMILEScopy InChI
Affinity DataKi:  3.30E+4nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50299462(2-(3-(dihydroxymethyl)naphthalen-2-ylamino)-2-oxoa...)copy SMILEScopy InChI
Affinity DataKi:  4.50E+4nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118762(2-(Oxalyl-amino)-4,5,6,7-tetrahydro-benzo[b]thioph...)copy SMILEScopy InChI
Affinity DataKi:  4.50E+4nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118796(6-(OXALYL-AMINO)-1H-INDOLE-5-CARBOXYLIC ACID | 6-(...)copy SMILEScopy InChI
Affinity DataKi:  6.60E+4nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118789(2-(oxaloamino)benzoic acid | CHEMBL139050)copy SMILEScopy InChI
Affinity DataKi:  1.30E+5nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118779(3-(Oxalyl-amino)-thiophene-2-carboxylic acid | 3-(...)copy SMILEScopy InChI
Affinity DataKi:  3.60E+5nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50299461((S)-7-(1,1-Dioxo-1H-1lambda*6*-benzo[d]isothiazol-...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+5nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118749(2-(Oxalyl-amino)-thiophene-3-carboxylic acid | 2-(...)copy SMILEScopy InChI
Affinity DataKi:  7.40E+5nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50118792(2-(OXALYL-AMINO)-4,5,6,7-TETRAHYDRO-THIENO[2,3-C]P...)copy SMILEScopy InChI
Affinity DataKi:  1.10E+6nMAssay Description:Inhibition of PTPREMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29023T5PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50450426(CHEMBL4174865)copy SMILEScopy InChI
Affinity DataIC50: 1.86E+3nMAssay Description:Inhibition of recombinant human cytosolic PTPepsilon expressed in Escherichia coli BL21 (DE3) using E527-P-Q-pY530-Q-P-G-E-N-L536 as substrate after ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C20F9PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50450424(CHEMBL4160163)copy SMILEScopy InChI
Affinity DataIC50: 2.01E+3nMAssay Description:Inhibition of recombinant human cytosolic PTPepsilon expressed in Escherichia coli BL21 (DE3) using E527-P-Q-pY530-Q-P-G-E-N-L536 as substrate after ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C20F9PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50450422(CHEMBL4170383)copy SMILEScopy InChI
Affinity DataIC50: 2.47E+3nMAssay Description:Inhibition of recombinant human cytosolic PTPepsilon expressed in Escherichia coli BL21 (DE3) using E527-P-Q-pY530-Q-P-G-E-N-L536 as substrate after ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C20F9PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50450423(CHEMBL4168082)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibition of recombinant human cytosolic PTPepsilon expressed in Escherichia coli BL21 (DE3) using E527-P-Q-pY530-Q-P-G-E-N-L536 as substrate after ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C20F9PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50450425(CHEMBL4159748)copy SMILEScopy InChI
Affinity DataIC50: 4.17E+3nMAssay Description:Inhibition of recombinant human cytosolic PTPepsilon expressed in Escherichia coli BL21 (DE3) using E527-P-Q-pY530-Q-P-G-E-N-L536 as substrate after ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C20F9PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM231167(US9340574, 7)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMpH: 7.0Assay 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 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NV9H4JUS Patent
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50607111(CHEMBL5218807)copy SMILES
Affinity DataIC50: 1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1HGFPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50054344(CHEMBL3319356 | US9522881, 11a-1 L97M74 | US984453...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of PTPepsilon (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24X59FMPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50054344(CHEMBL3319356 | US9522881, 11a-1 L97M74 | US984453...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:For selectivity studies, the PTPs, including LYP, mPTPA, SHP1-D1C, PTP1B, LMPTP, VHR, Laforin and PTPα-D1D2 were expressed and purified from E. ...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DN4402US Patent
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50436357(CHEMBL2396719)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of recombinant PTPepsilon (unknown origin) using pNPP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N017XWPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50436358(CHEMBL2396718)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of recombinant PTPepsilon (unknown origin) using pNPP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N017XWPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50544431(CHEMBL4637459 | US11192850, Entry 4k)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of PTPE (unknown origin) expressed in Escherichia coli BL21 using p-nitrophenyl phosphate as substrate measured after 30 mins by UV-vis sp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3R3BPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50544440(CHEMBL4647367 | US11192850, Entry 4t)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of PTPE (unknown origin) expressed in Escherichia coli BL21 using p-nitrophenyl phosphate as substrate measured after 30 mins by UV-vis sp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3R3BPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50246580((S)-2-((4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50222205((1S,2R,4aS,6aS,6bR,8aR,10R,11R,12aR,12bR,14bS)-10,...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50148911((3beta)-3-hydroxyurs-12-en-28-oic acid | 3beta-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50079577((4aS,6aS,6bR,10S,12aR,14bS)-10-Hydroxy-2,2,6a,6b,9...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50246620(3-((4aR,6aS,6bR,8aR,10S,12aR,12bR,14bR)-10-hydroxy...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50246621(5-((4aR,6aS,6bR,8aR,10S,12aR,12bR,14bR)-10-hydroxy...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50246745(3-(4-Carboxy-benzyloxy)-28-[4-butyric ((S)-1-carbo...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50246744((4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-(4-carboxy...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50246653((S)-2-(5-((4aR,6aS,6bR,8aR,10S,12aR,12bR,14bR)-10-...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50246668(3-(benzo[d][1,3]dioxol-5-yl)-2-(5-((4aR,6aS,6bR,8a...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50194130((4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-(3-carboxy...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human recombinant PTPepsilonMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HX1CH7PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50544427(CHEMBL4632818 | US11192850, Entry 4g)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of PTPE (unknown origin) expressed in Escherichia coli BL21 using p-nitrophenyl phosphate as substrate measured after 30 mins by UV-vis sp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QV3R3BPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50112358(CHEMBL3609374)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of phosphatase activity of human PTPepsilon using pNPP as a substrate after 10 mins by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251M0SPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50112357(CHEMBL3609375)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of phosphatase activity of human PTPepsilon using pNPP as a substrate after 10 mins by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251M0SPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50087856(CHEMBL3426913)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMpH: 7.0Assay Description:Inhibition of PTPepsilon (unknown origin) using pNPP as substrate at pH 7 at 25 degC by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VD7168PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50112356(CHEMBL3609373)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of phosphatase activity of human PTPepsilon using pNPP as a substrate after 10 mins by spectrophotometer analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2251M0SPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50263036(3-Hydroxy-6-methoxy-8,8-dimethyl-1-oxo-1,3,4,7,8,9...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PTPep (unknown origin) using DiFMUP as substrate incubated for 30 mins followed by substrate addition at pH 6.5 by standard phosphatase...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7KRWPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50262987(CHEMBL506661 | Illudalic acid)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PTPep (unknown origin) using DiFMUP as substrate incubated for 30 mins followed by substrate addition at pH 6.5 by standard phosphatase...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7KRWPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50262987(CHEMBL506661 | Illudalic acid)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PTPep (unknown origin) using DiFMUP as substrate incubated for 30 mins followed by substrate addition at pH 6.5 by standard phosphatase...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7KRWPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50263036(3-Hydroxy-6-methoxy-8,8-dimethyl-1-oxo-1,3,4,7,8,9...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of PTPep (unknown origin) using DiFMUP as substrate incubated for 30 mins followed by substrate addition at pH 6.5 by standard phosphatase...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7KRWPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50558485(CHEMBL4800195)copy SMILES
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of His-tagged PTPepsilon (unknown origin) expressed in Escherichia coli BL21 cells using para-nitrophenyl phosphate as substrate incubated...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DN48Q4PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50607110(CHEMBL5219519)copy SMILES
Affinity DataIC50: 1.00E+5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1HGFPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50558461(CHEMBL4760367)copy SMILES
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of His-tagged PTPepsilon (unknown origin) expressed in Escherichia coli BL21 cells using para-nitrophenyl phosphate as substrate incubated...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DN48Q4PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50558488(CHEMBL4794972)copy SMILES
Affinity DataIC50: 2.00E+5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1HGFPubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50558488(CHEMBL4794972)copy SMILES
Affinity DataIC50: 2.00E+5nMAssay Description:Inhibition of His-tagged PTPepsilon (unknown origin) expressed in Escherichia coli BL21 cells using para-nitrophenyl phosphate as substrate incubated...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DN48Q4PubMed
TargetReceptor-type tyrosine-protein phosphatase epsilon(Homo sapiens (Human))
University of Miami

Curated by ChEMBL
LigandPNGBDBM50558487(CHEMBL4786243)copy SMILES
Affinity DataIC50: 2.00E+5nMAssay Description:Inhibition of His-tagged PTPepsilon (unknown origin) expressed in Escherichia coli BL21 cells using para-nitrophenyl phosphate as substrate incubated...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DN48Q4PubMed
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