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Assay Detail

CHEMBL3384852

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

Binding
Inhibition of human NPP1 using p-Nph-5'-TMP as substrate
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Publication

Imidazopyridine- and purine-thioacetamide derivatives: potent inhibitors of nucleotide pyrophosphatase/phosphodiesterase 1 (NPP1).
Chang L, Lee SY, Leonczak P, Rozenski J, De Jonghe S, Hanck T, Müller CE, Herdewijn P.
J Med Chem (2014) 57 : 10080 -10100
PubMed 25372276 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 17 6.63 8.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3360892 1 8.30
CHEMBL3360893 1 7.70
CHEMBL3360884 1 7.53
CHEMBL3360901 1 7.45
CHEMBL3360878 1 7.36
CHEMBL3360885 1 6.90
CHEMBL3360880 1 6.88
CHEMBL3360882 1 6.86
CHEMBL3360899 1 6.82
CHEMBL3360883 1 6.72
CHEMBL1433061 1 6.66
CHEMBL3360879 1 6.55
CHEMBL3360895 1 6.00
CHEMBL3360897 1 5.46
CHEMBL3360898 1 5.44
CHEMBL3360894 1 5.09
CHEMBL3360896 1 4.96

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3360892 Ki = 5.0 nM 8.30
CHEMBL3360893 Ki = 20.0 nM 7.70
CHEMBL3360884 Ki = 29.6 nM 7.53
CHEMBL3360901 Ki = 35.8 nM 7.45
CHEMBL3360878 Ki = 44.2 nM 7.36
CHEMBL3360885 Ki = 127.0 nM 6.90
CHEMBL3360880 Ki = 131.0 nM 6.88
CHEMBL3360882 Ki = 137.0 nM 6.86
CHEMBL3360899 Ki = 152.0 nM 6.82
CHEMBL3360883 Ki = 192.0 nM 6.72
CHEMBL1433061 Ki = 217.0 nM 6.66
CHEMBL3360879 Ki = 281.0 nM 6.55
CHEMBL3360895 Ki = 1010.0 nM 6.00
CHEMBL3360897 Ki = 3480.0 nM 5.46
CHEMBL3360898 Ki = 3650.0 nM 5.44
CHEMBL3360894 Ki = 8040.0 nM 5.09
CHEMBL3360896 Ki = 11000.0 nM 4.96