Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond
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Open Source Drug Discovery: Highly Potent Antimalarial Compounds Derived from the Tres Cantos ArylpyrrolesMuddled mechanisms: recent progress towards antimalarial target identificationAn open source pharma roadmapIdentification of inhibitors that dually target the new permeability pathway and dihydroorotate dehydrogenase in the blood stage of Plasmodium falciparumThe Malaria Parasite's Lactate Transporter PfFNT Is the Target of Antiplasmodial Compounds Identified in Whole Cell Phenotypic ScreensEsterase mutation is a mechanism of resistance to antimalarial compoundsNovel lead structures with both Plasmodium falciparum gametocytocidal and asexual blood stage activity identified from high throughput compound screeningDeveloping transmission-blocking strategies for malaria control.Reliance of Wolbachia on High Rates of Host Proteolysis Revealed by a Genome-Wide RNAi Screen of Drosophila Cells.Discovery of a Novel Antifungal Agent in the Pathogen Box.Metabolomic Profiling of the Malaria Box Reveals Antimalarial Target Pathways.Herbicidal properties of antimalarial drugs.The need to compare: assessing the level of agreement of three high-throughput assays against Plasmodium falciparum mature gametocytes.Screening the Medicines for Malaria Venture Pathogen Box across Multiple Pathogens Reclassifies Starting Points for Open-Source Drug Discovery.The Candidate Antimalarial Drug MMV665909 Causes Oxygen-Dependent mRNA Mistranslation and Synergizes with Quinoline-Derived Antimalarials.Modulation of Antimalarial Activity at a Putative Bisquinoline Receptor In Vivo Using Fluorinated Bisquinolines.A validated bioluminescence-based assay for the rapid determination of the initial rate of kill for discovery antimalarials.Antimalarial activity of Malaria Box Compounds against Plasmodium falciparum clinical isolates.Biological Studies and Target Engagement of the 2-C-Methyl-d-Erythritol 4-Phosphate Cytidylyltransferase (IspD)-Targeting Antimalarial Agent (1R,3S)-MMV008138 and Analogs.malERA: An updated research agenda for basic science and enabling technologies in malaria elimination and eradication.An automated high-throughput system for phenotypic screening of chemical libraries on C. elegans and parasitic nematodes.Clinical and microbiologic efficacy of the piperazine-based drug lead MMV665917 in the dairy calf cryptosporidiosis model.Characterization of Plasmodium Atg3-Atg8 interaction inhibitors identifies novel alternative mechanisms of action in Toxoplasma gondii.Exploiting the Evolutionary Relationship between Malarial Parasites and Plants To Develop New Herbicides.Recent buzz in malaria research.Discovery of New Inhibitors of Toxoplasma gondii via the Pathogen Box.Specific Inhibition of the Bifunctional Farnesyl/Geranylgeranyl Diphosphate Synthase in Malaria Parasites via a New Small-Molecule Binding Site.A Novel Piperazine-Based Drug Lead for Cryptosporidiosis from the Medicines for Malaria Venture Open Access Malaria Box.Targeted Phenotypic Screening in Plasmodium falciparum and Toxoplasma gondii Reveals Novel Modes of Action of Medicines for Malaria Venture Malaria Box Molecules.Fragment-Based Screening of a Natural Product Library against 62 Potential Malaria Drug Targets Employing Native Mass Spectrometry.Progress in the pharmacological treatment of human cystic and alveolar echinococcosis: Compounds and therapeutic targets.Novel Antifungal Compounds Discovered in Medicines for Malaria Venture's Malaria Box.Screening a repurposing library, the Medicines for Malaria Venture Stasis Box, against Schistosoma mansoni.Diverse antimalarials from whole-cell phenotypic screens disrupt malaria parasite ion and volume homeostasis.Evaluation of Current and Emerging Antimalarial Medicines for Inhibition of Toxoplasma gondii Growth in VitroAntimalarial agents against both sexual and asexual parasites stages: structure-activity relationships and biological studies of the Malaria Box compound 1-[5-(4-bromo-2-chlorophenyl)furan-2-yl]-N-[(piperidin-4-yl)methyl]methanamine (MMV019918) and aCurrent Screening Methodologies in Drug Discovery for Selected Human DiseasesRepurposing of an old drug: In vitro and in vivo efficacies of buparvaquone against Echinococcus multilocularisRecent Breakthroughs and Ongoing Limitations in ResearchScreening for potential prophylactics targeting sporozoite motility through the skin
P2860
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P2860
Open Source Drug Discovery with the Malaria Box Compound Collection for Neglected Diseases and Beyond
description
2016 nî lūn-bûn
@nan
2016 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@ast
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@en
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@nl
type
label
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@ast
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@en
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@nl
prefLabel
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@ast
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@en
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@nl
P2093
P2860
P50
P921
P3181
P1433
P1476
Open Source Drug Discovery wit ...... Neglected Diseases and Beyond
@en
P2093
Abhai K Tripathi
Ainhoa Alzualde
Aintzane Alday
Aishah Alsibaee
Alvine N Mfopa
Amornrat Naranuntarat Jensen
Andreas Spitzmüller
Andrew F Wilks
Andrew Hemphill
Ani Galstian
P2860
P304
P3181
P356
10.1371/JOURNAL.PPAT.1005763
P407
P50
P577
2016-07-01T00:00:00Z