25 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
24359257	10	Optimization of furin inhibitors to protect against the activation of influenza hemagglutinin H5 and Shiga toxin.	Universit£
24350995	46	Design, synthesis, and structure-activity relationship studies of a potent PACE4 inhibitor.	Universit£
23126600	34	The Multi-Leu peptide inhibitor discriminates between PACE4 and furin and exhibits antiproliferative effects on prostate cancer cells.	Universit£
22682919	26	Furin inhibitors: importance of the positive formal charge and beyond.	Torrey Pines Institute For Molecular Studies
21757345	34	New substrate analogue furin inhibitors derived from 4-amidinobenzylamide.	Philipps University Marburg
21168329	47	New furin inhibitors based on weakly basic amidinohydrazones.	Philipps University Marburg
20045647	35	Synthesis and optimization of thiadiazole derivatives as a novel class of substrate competitive c-Jun N-terminal kinase inhibitors.	Institute For Medical Research
20038105	50	Potent inhibitors of furin and furin-like proprotein convertases containing decarboxylated P1 arginine mimetics.	Philipps University Marburg
19282190	4	Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitors.	Institute For Medical Research
18977558	18	Modeling the activity of furin inhibitors using artificial neural network.	Mahidol University
17537721	289	Targeting host cell furin proprotein convertases as a therapeutic strategy against bacterial toxins and viral pathogens.	Institute For Medical Research
27045975	34	Notch Antagonists: Potential Modulators of Cancer and Inflammatory Diseases.	Centre Hospitalier Universitaire Vaudois (Chuv)
7562936	10	Synthesis of tight binding inhibitors and their action on the proprotein-processing enzyme furin.	Friedrich Miescher-Institut
30501188	24	Improving the Selectivity of PACE4 Inhibitors through Modifications of the P1 Residue.	TBA
30180568	54	Increasing C-Terminal Hydrophobicity Improves the Cell Permeability and Antiproliferative Activity of PACE4 Inhibitors against Prostate Cancer Cell Lines.	Universit£
28287731	150	Positional Scanning Identifies the Molecular Determinants of a High Affinity Multi-Leucine Inhibitor for Furin and PACE4.	University of Gdansk