I-C11 [Ligand Id: 10374] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL260920
  • protein tyrosine phosphatase non-receptor type 22/Hematopoietic cell protein-tyrosine phosphatase 70Z-PEP in Human [ChEMBL: CHEMBL2889] [GtoPdb: 3084] [UniProtKB: Q9Y2R2]
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  • protein tyrosine phosphatase non-receptor type 1/Protein-tyrosine phosphatase 1B in Human [ChEMBL: CHEMBL335] [GtoPdb: 2976] [UniProtKB: P18031]
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  • Protein-tyrosine phosphatase 1E in Human [ChEMBL: CHEMBL2976] [UniProtKB: Q12923]
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  • protein tyrosine phosphatase non-receptor type 11/Protein-tyrosine phosphatase 2C in Human [ChEMBL: CHEMBL3864] [GtoPdb: 3203] [UniProtKB: Q06124]
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  • Protein-tyrosine phosphatase LC-PTP in Human [ChEMBL: CHEMBL2219] [UniProtKB: P35236]
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  • Tyrosine-protein phosphatase non-receptor type 9 in Human [ChEMBL: CHEMBL6117] [UniProtKB: P43378]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
protein tyrosine phosphatase non-receptor type 22/Hematopoietic cell protein-tyrosine phosphatase 70Z-PEP in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2889] [GtoPdb: 3084] [UniProtKB: Q9Y2R2]
ChEMBL Inhibition of LYP expressed in Escherichia coli BL21 using increasing levels of ARLIED-NEpYTAREG substrate B 4.47 pKi 33870 nM Ki J Med Chem (2011) 54: 1640-1654 [PMID:21341673]
ChEMBL Competitive inhibition of N-terminal 6xHis-tagged LYP catalytic domain (1 to 303) (unknown origin) expressed in Escherichia coli BL21(DE3) using pNPP as substrate by Dixon plot analysis B 5.54 pKi 2900 nM Ki J Med Chem (2013) 56: 4990-5008 [PMID:23713581]
GtoPdb - - 5.54 pKi 2900 nM Ki Proc Natl Acad Sci USA (2007) 104: 19767-72 [PMID:18056643]
ChEMBL Inhibition of lymphoid-specific tyrosine phosphatase F28A mutant B 4.46 pIC50 35000 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
ChEMBL Inhibition of lymphoid-specific tyrosine phosphatase S35E mutant B 4.68 pIC50 21000 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
ChEMBL Inhibition of lymphoid-specific tyrosine phosphatase K138A mutant B 4.72 pIC50 19000 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
ChEMBL Inhibition of lymphoid-specific tyrosine phosphatase R33A mutant B 4.9 pIC50 12500 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
ChEMBL Inhibition of lymphoid-specific tyrosine phosphatase L29A mutant B 4.93 pIC50 11800 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
ChEMBL Inhibition of lymphoid-specific tyrosine phosphatase C129S mutant B 5.09 pIC50 8100 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
ChEMBL Inhibition of lymphoid-specific tyrosine phosphatase B 5.34 pIC50 4600 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
ChEMBL Inhibition of Lyp-mediated pNPP hydrolysis B 5.34 pIC50 4600 nM IC50 Bioorg Med Chem (2012) 20: 1940-1946 [PMID:22133902]
ChEMBL Inhibition of N-terminal 6xHis-tagged LYP catalytic domain (1 to 294) (unknown origin) expressed in Escherichia coli BL21(DE3) using pNPP as substrate by spectrometric analysis B 5.34 pIC50 4600 nM IC50 J Med Chem (2013) 56: 4990-5008 [PMID:23713581]
GtoPdb In vitro measurement of PTPN22-catalysed substrate dephosphorylation, using pNPP as a substrate at pH 7.0, 25°C, and ionic strength of 0.15 M. - 5.34 pIC50 4600 nM IC50 Proc Natl Acad Sci USA (2007) 104: 19767-72 [PMID:18056643]
ChEMBL Inhibition of recombinant LyP assessed as hydrolysis of DiFMUP B 5.35 pIC50 4500 nM IC50 J Med Chem (2011) 54: 562-571 [PMID:21190368]
ChEMBL Inhibition of lymphoid-specific tyrosine phosphatase T36E mutant B 5.55 pIC50 2800 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
protein tyrosine phosphatase non-receptor type 1/Protein-tyrosine phosphatase 1B in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL335] [GtoPdb: 2976] [UniProtKB: P18031]
ChEMBL Inhibition of PTP1B B 4.93 pIC50 11800 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
GtoPdb - - 4.93 pIC50 11800 nM IC50 Proc Natl Acad Sci USA (2007) 104: 19767-72 [PMID:18056643]
Protein-tyrosine phosphatase 1E in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2976] [UniProtKB: Q12923]
ChEMBL Inhibition of FAP1 B 4.43 pIC50 36800 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
protein tyrosine phosphatase non-receptor type 11/Protein-tyrosine phosphatase 2C in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3864] [GtoPdb: 3203] [UniProtKB: Q06124]
ChEMBL Inhibition of SHP2 B 4.44 pIC50 36000 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
Protein-tyrosine phosphatase LC-PTP in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2219] [UniProtKB: P35236]
ChEMBL Inhibition of HePTP B 4.49 pIC50 32100 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]
Tyrosine-protein phosphatase non-receptor type 9 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL6117] [UniProtKB: P43378]
ChEMBL Inhibition of PTP-Meg2 B 4.5 pIC50 31800 nM IC50 Proc Natl Acad Sci U S A (2007) 104: 19767-19772 [PMID:18056643]

ChEMBL data shown on this page come from version 33:

Mendez D, Gaulton A, Bento AP, Chambers J, De Veij M, Félix E, Magariños MP, Mosquera JF, Mutowo P, Nowotka M, Gordillo-Marañón M, Hunter F, Junco L, Mugumbate G, Rodriguez-Lopez M, Atkinson F, Bosc N, Radoux CJ, Segura-Cabrera A, Hersey A, Leach AR. (2019) 'ChEMBL: towards direct deposition of bioassay data' Nucleic Acids Res., 47(D1). DOI: 10.1093/nar/gky1075. [EPMCID:30398643]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]