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Synthesis of a New Peptide–Coumarin Conjugate: A Potential Agent against Cryptococcosis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes
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Ubiquicidin, a novel murine microbicidal protein present in the cytosolic fraction of macrophages
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Synthesis, characterization, and antimicrobial activity of some new coumarin derivatives
inferredcites →https://doi.org/10.1007/s10096-013-1915-8openalex-snapshot
Cryptococcosis: epidemiology, fungal resistance, and new alternatives for treatment
inferredcites →https://doi.org/10.1016/j.bbagen.2011.08.011openalex-snapshot
The antimicrobial peptide arenicin-1 promotes generation of reactive oxygen species and induction of apoptosis
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Melittin induces apoptotic features in Candida albicans
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Induction of yeast apoptosis by an antimicrobial peptide, Papiliocin
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Synthesis and evaluation of a class of new coumarin triazole derivatives as potential antimicrobial agents
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A Common Mechanism of Cellular Death Induced by Bactericidal Antibiotics
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Synthesis of uriedo and thiouriedo derivatives of peptide conjugated heterocycles – A new class of promising antimicrobials
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Synthetic peptides derived from human antimicrobial peptide ubiquicidin accumulate at sites of infections and eradicate (multi-drug resistant) Staphylococcus aureus in mice
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Amphotericin B: side effects and toxicity
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Molecular Basis for Membrane Selectivity of an Antimicrobial Peptide, Magainin 2
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Peptide Cyclization and Cyclodimerization by CuI-Mediated Azide−Alkyne Cycloaddition
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A Fluorogenic 1,3-Dipolar Cycloaddition Reaction of 3-Azidocoumarins and Acetylenes
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Antimicrobial peptides of multicellular organisms
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Potentiating antibacterial activity by predictably enhancing endogenous microbial ROS production
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How antibiotics kill bacteria: new models needed?
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Peptidomimetics via copper-catalyzed azide–alkyne cycloadditions
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Basis for Selectivity of Cationic Antimicrobial Peptides for Bacterial Versus Mammalian Membranes
inferredcites →https://doi.org/10.1093/jac/dkt114openalex-snapshot
The role of oxidative and nitrosative bursts caused by azoles and amphotericin B against the fungal pathogen Cryptococcus gattii
inferredcites →https://doi.org/10.1111/j.1939-165x.2010.00281.xopenalex-snapshot
Cryptococcosis: update and emergence ofCryptococcus gattii
inferredcites →https://doi.org/10.1128/aac.00153-10openalex-snapshot
Heteroresistance of Cryptococcus gattii to Fluconazole
inferredcites →https://doi.org/10.1128/aac.46.6.1634-1639.2002openalex-snapshot
Internal Thiols and Reactive Oxygen Species in Candidacidal Activity Exerted by an N-Terminal Peptide of Human Lactoferrin
inferredcites →https://doi.org/10.1128/ec.2.4.655-663.2003openalex-snapshot
A Yeast under Cover: the Capsule ofCryptococcus neoformans
inferredcites →https://doi.org/10.1128/jcm.41.1.267-272.2003openalex-snapshot
Characterization of Heteroresistance to Fluconazole among Clinical Isolates of Cryptococcus neoformans
inferredcites →https://doi.org/10.1211/0022357022971openalex-snapshot
Histatins: antimicrobial peptides with therapeutic potential
inferredcites →https://doi.org/10.1371/journal.pone.0112669openalex-snapshot
Fluconazole Alters the Polysaccharide Capsule of Cryptococcus gattii and Leads to Distinct Behaviors in Murine Cryptococcosis
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Triazole Antifungal Agents in Invasive Fungal Infections
inferredcites →https://doi.org/10.2174/092986712803414213openalex-snapshot
Recent Researches in Triazole Compounds as Medicinal Drugs
inferredcites →https://doi.org/10.2174/1381612811319210013openalex-snapshot
Current Developments of Coumarin Compounds in Medicinal Chemistry
inferredcites →https://doi.org/10.2174/138945005774912753openalex-snapshot
Detection of Fungal Infections Using Radiolabeled Antifungal Agents
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Antimicrobial Peptides for Therapeutic Applications: A Review
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Peptide Conjugation via CuAAC ‘Click’ Chemistry
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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