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Assay Detail

CHEMBL4688203

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

Binding
Inhibition of human recombinant Pin1 using Suc-AEPF-NH-Np as substrate by alpha-chymotrypsin based assay
1
Total Activities
1
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

Target

Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (CHEMBL2288)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis and biological evaluation of novel thiazole-based derivatives as human Pin1 inhibitors.
Du L,Wang X,Cui G,Xu B
Bioorg Med Chem (2021) 29 : 115878 -115878
PubMed 33246256 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 5.30 5.30

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL55934 NAPHTHOQUINONE 1 5.30

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL55934 NAPHTHOQUINONE IC50 = 5000.0 nM 5.30