30 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
Identification of novel class of falcipain-2 inhibitors as potential antimalarial agents.
University of Toronto
Synthesis of gallinamide A analogues as potent falcipain inhibitors and antimalarials.
The University of Sydney
Constrained peptidomimetics as antiplasmodial falcipain-2 inhibitors.
University of Messina
Development of peptidomimetics with a vinyl sulfone warhead as irreversible falcipain-2 inhibitors.
University of Messina
Identification of novel parasitic cysteine protease inhibitors using virtual screening. 1. The ChemBridge database.
University of Mississippi
Novel peptidomimetic cysteine protease inhibitors as potential antimalarial agents.
University of Messina
Identification of novel parasitic cysteine protease inhibitors by use of virtual screening. 2. The available chemical directory.
University of Mississippi
Synthesis of novel peptidomimetics as inhibitors of protozoan cysteine proteases falcipain-2 and rhodesain.
University of Messina
Design and synthesis of novel 2-pyridone peptidomimetic falcipain 2/3 inhibitors.
University of Algarve
A prodomain peptide of Plasmodium falciparum cysteine protease (falcipain-2) inhibits malaria parasite development.
International Center For Genetic Engineering and Biotechnology
Design, synthesis, and antimalarial activity of structural chimeras of thiosemicarbazone and ferroquine analogues.
Université
New structural classes of antimalarials.
National Institute of Pharmaceutical Education and Research (NIPER)
Reinvestigation of diphenylmethylpiperazine analogues of pyrazine as new class of
Jamia Millia Islamia (A Central University)
Is structural hybridization invoking new dimensions for antimalarial drug discovery research?
University of Delhi
Falcipains: Biochemistry, target validation and structure-activity relationship studies of inhibitors as antimalarials.
University of Petroleum and Energy Studies
Dipeptide vinyl sultams: synthesis via the Wittig-Horner reaction and activity against papain, falcipain-2 and Plasmodium falciparum.
University of Lisbon
Discovery of potent thiosemicarbazone inhibitors of rhodesain and cruzain.
University of California San Francisco
Synthesis and structure-activity relationships of parasiticidal thiosemicarbazone cysteine protease inhibitors against Plasmodium falciparum, Trypanosoma brucei, and Trypanosoma cruzi.
University of California San Francisco
Synthesis and evaluation of isatins and thiosemicarbazone derivatives against cruzain, falcipain-2 and rhodesain.
University of Cape Town
Identification of antimalarial leads with dual falcipain-2 and falcipain-3 inhibitory activity.
Shoolini University of Biotechnology and Management Sciences
Recent advances of tetrazole derivatives as potential anti-tubercular and anti-malarial agents.
Wuxi Apptec
Falcipain Inhibitors Based on the Natural Product Gallinamide A Are Potent in Vitro and in Vivo Antimalarials.
The University of Sydney
Synthesis and antimalarial effects of phenothiazine inhibitors of a Plasmodium falciparum cysteine protease.
Universidad Central De Venezuela
New aziridine-based inhibitors of cathepsin L-like cysteine proteases with selectivity for the Leishmania cysteine protease LmCPB2.8.
Johannes Gutenberg-Universit£T Mainz
Peptidomimetic nitrile inhibitors of malarial protease falcipain-2 with high selectivity against human cathepsins.
Irbm Science Park
Designing novel inhibitors against falcipain-2 of Plasmodium falciparum.
Delhi Institute of Pharmaceutical Sciences and Research
Quinoline hybrids and their antiplasmodial and antimalarial activities.
Hubei Engineering University
Development of Novel Peptide-Based Michael Acceptors Targeting Rhodesain and Falcipain-2 for the Treatment of Neglected Tropical Diseases (NTDs).
University of Messina
