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Assay Detail

CHEMBL770122

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of human Protein-tyrosine phosphatase 1B (PTP1B) using fluorescein diphosphate (FDP)
13
Total Activities
13
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

Tyrosine-protein phosphatase non-receptor type 1 (CHEMBL335)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and PTP1B inhibition of 1,2-naphthoquinone derivatives as potent anti-diabetic agents.
Ahn JH, Cho SY, Ha JD, Chu SY, Jung SH, Jung YS, Baek JY, Choi IK, Shin EY, Kang SK, Kim SS, Cheon HG, Yang SD, Choi JK.
Bioorg Med Chem Lett (2002) 12 : 1941 -1946
PubMed 12113814 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 6.11 6.57

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL61186 1 6.57
CHEMBL58848 1 6.48
CHEMBL301909 1 6.37
CHEMBL57157 1 6.21
CHEMBL56948 1 6.19
CHEMBL60918 1 6.17
CHEMBL60763 1 6.04
CHEMBL58032 1 6.03
CHEMBL292444 1 6.00
CHEMBL57841 1 6.00
CHEMBL58354 1 5.83
CHEMBL301436 1 5.81
CHEMBL52347 1,2-NAPHTHOQUINONE 1 5.79

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL61186 IC50 = 270.0 nM 6.57
CHEMBL58848 IC50 = 330.0 nM 6.48
CHEMBL301909 IC50 = 430.0 nM 6.37
CHEMBL57157 IC50 = 610.0 nM 6.21
CHEMBL56948 IC50 = 650.0 nM 6.19
CHEMBL60918 IC50 = 680.0 nM 6.17
CHEMBL60763 IC50 = 920.0 nM 6.04
CHEMBL58032 IC50 = 940.0 nM 6.03
CHEMBL292444 IC50 = 1010.0 nM 6.00
CHEMBL57841 IC50 = 1010.0 nM 6.00
CHEMBL58354 IC50 = 1480.0 nM 5.83
CHEMBL301436 IC50 = 1540.0 nM 5.81
CHEMBL52347 1,2-NAPHTHOQUINONE IC50 = 1640.0 nM 5.79