14 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Optimization of furin inhibitors to protect against the activation of influenza hemagglutinin H5 and Shiga toxin.
Universit£
Design, synthesis, and structure-activity relationship studies of a potent PACE4 inhibitor.
Universit£
The Multi-Leu peptide inhibitor discriminates between PACE4 and furin and exhibits antiproliferative effects on prostate cancer cells.
Universit£
Furin inhibitors: importance of the positive formal charge and beyond.
Torrey Pines Institute For Molecular Studies
New substrate analogue furin inhibitors derived from 4-amidinobenzylamide.
Philipps University Marburg
New furin inhibitors based on weakly basic amidinohydrazones.
Philipps University Marburg
Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitors.
Institute For Medical Research
Potent inhibitors of furin and furin-like proprotein convertases containing decarboxylated P1 arginine mimetics.
Philipps University Marburg
Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitors.
Institute For Medical Research
Modeling the activity of furin inhibitors using artificial neural network.
Mahidol University
Targeting host cell furin proprotein convertases as a therapeutic strategy against bacterial toxins and viral pathogens.
Institute For Medical Research
Synthesis of tight binding inhibitors and their action on the proprotein-processing enzyme furin.
Friedrich Miescher-Institut