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N6-modification of 7-deazapurine nucleoside analogues as anti-Trypanosoma cruzi and anti-Leishmania agents : structure-activity relationship exploration and in vivo evaluation
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2-((3,5-Dinitrobenzyl)thio)quinazolinones : potent antimycobacterial agents activated by deazaflavin (F420)-dependent nitroreductase (Ddn)
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6‐methyl‐7‐aryl‐7‐deazapurine nucleosides as anti‐trypanosoma cruzi agents : structure‐activity relationship and in vivo efficacy
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4E interacting protein as a potential novel drug target for nucleoside analogues in Trypanosoma brucei
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Structure-activity relationship exploration of 3’-deoxy-7-deazapurine nucleoside analogues as anti-Trypanosoma brucei agents
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Combining tubercidin and cordycepin scaffolds results in highly active candidates to treat late-stage sleeping sickness
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Revisiting tubercidin against kinetoplastid parasites : aromatic substitutions at position 7 improve activity and reduce toxicity
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Targeting an aromatic hotspot in Plasmodium falciparum 1-deoxy-d-xylulose-5-phosphate reductoisomerase with β-arylpropyl analogues of fosmidomycin
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Exploring the purine core of 3'-C-ethynyladenosine (EAdo) in search of novel nucleoside therapeutics
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Drug design and identification of potent leads against Mycobacterium tuberculosis thymidine monophosphate kinase