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Assay Detail

CHEMBL871238

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Binding
Inhibition of human recombinant PRL-3
15
Total Activities
15
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Expert

Target

Protein tyrosine phosphatase type IVA 3 (CHEMBL4162)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and biological evaluation of rhodanine derivatives as PRL-3 inhibitors.
Ahn JH, Kim SJ, Park WS, Cho SY, Ha JD, Kim SS, Kang SK, Jeong DG, Jung SK, Lee SH, Kim HM, Park SK, Lee KH, Lee CW, Ryu SE, Choi JK.
Bioorg Med Chem Lett (2006) 16 : 2996 -2999
PubMed 16530413 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 15 5.57 6.05

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL207428 1 6.05
CHEMBL207958 1 6.05
CHEMBL379654 1 5.92
CHEMBL209088 1 5.80
CHEMBL206365 1 5.77
CHEMBL183838 1 5.77
CHEMBL378022 1 5.72
CHEMBL206973 1 5.70
CHEMBL379422 1 5.62
CHEMBL186892 1 5.52
CHEMBL210772 1 5.51
CHEMBL207365 1 5.43
CHEMBL206414 1 5.40
CHEMBL210039 1 5.02
CHEMBL55 PENTAMIDINE 4.0 1 4.27

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL207428 IC50 = 900.0 nM 6.05
CHEMBL207958 IC50 = 900.0 nM 6.05
CHEMBL379654 IC50 = 1200.0 nM 5.92
CHEMBL209088 IC50 = 1600.0 nM 5.80
CHEMBL206365 IC50 = 1700.0 nM 5.77
CHEMBL183838 IC50 = 1700.0 nM 5.77
CHEMBL378022 IC50 = 1900.0 nM 5.72
CHEMBL206973 IC50 = 2000.0 nM 5.70
CHEMBL379422 IC50 = 2400.0 nM 5.62
CHEMBL186892 IC50 = 3000.0 nM 5.52
CHEMBL210772 IC50 = 3100.0 nM 5.51
CHEMBL207365 IC50 = 3700.0 nM 5.43
CHEMBL206414 IC50 = 4000.0 nM 5.40
CHEMBL210039 IC50 = 9500.0 nM 5.02
CHEMBL55 PENTAMIDINE IC50 = 53600.0 nM 4.27