about
Microbial pigments as natural color sources: current trends and future perspectivesBiosynthesis and molecular actions of specialized 1,4-naphthoquinone natural products produced by horticultural plantsNaphthoquinone derivatives exert their antitrypanosomal activity via a multi-target mechanismScreening of Potential anti-Trypanosoma cruzi Candidates: In Vitro and In Vivo Studies.Targeting the substrate preference of a type I nitroreductase to develop antitrypanosomal quinone-based prodrugs.Experimental Chemotherapy for Chagas Disease: A Morphological, Biochemical, and Proteomic Overview of Potential Trypanosoma cruzi Targets of Amidines Derivatives and Naphthoquinones.The Combination of Vitamin K3 and Vitamin C Has Synergic Activity against Forms of Trypanosoma cruzi through a Redox Imbalance Process.The naphthoquinone diospyrin is an inhibitor of DNA gyrase with a novel mechanism of action.Cytotoxicity and In Vitro Antileishmanial Activity of Antimony (V), Bismuth (V), and Tin (IV) Complexes of Lapachol.Effects of a novel β-lapachone derivative on Trypanosoma cruzi: Parasite death involving apoptosis, autophagy and necrosis.Reviews on 1,4-naphthoquinones from Diospyros L.The Role of Heme and Reactive Oxygen Species in Proliferation and Survival of Trypanosoma cruzi.Searching for a potential antibacterial lead structure against bacterial biofilms among new naphthoquinone compounds.Catalytic asymmetric reactions and synthesis of quinones.Novel naphthoquinone derivatives and evaluation of their trypanocidal and leishmanicidal activities.Distinct activation mechanisms trigger the trypanocidal activity of DNA damaging prodrugs.Evidence for Tissue Toxicity in BALB/c Exposed to a Long-Term Treatment with Oxiranes Compared to Meglumine AntimoniateEpoxy-α-lapachone has in vitro and in vivo anti-leishmania (Leishmania) amazonensis effects and inhibits serine proteinase activity in this parasite.Protonation Sites, Tandem Mass Spectrometry and Computational Calculations of o-Carbonyl Carbazolequinone Derivatives.Trypanosoma cruzi mitochondrial swelling and membrane potential collapse as primary evidence of the mode of action of naphthoquinone analogues.Experimental and Theoretical Reduction Potentials of Some Biologically Active ortho-Carbonyl para-Quinones.Copper(i)-Y zeolite catalyzed N-sulfonylketenimine mediated annulation of hydroxynaphthoquinones: syntheses of naphtho[2,1-b]furan-2,5-diones and benzo[de]chromene-2,6-diones.A novel triazolic naphthofuranquinone induces autophagy in reservosomes and impairment of mitosis in Trypanosoma cruzi.Synthesis, Characterization, and Antileukemic Properties of Naphthoquinone Derivatives of Lawsone.Lapachol suppresses cell proliferation and secretion of interleukin-6 and plasminogen activator inhibitor-1 of fibroblasts derived from hypertrophic scars.Activation of NAD(P)H:quinone oxidoreductase ameliorates spontaneous hypertension in an animal model via modulation of eNOS activity.Covalent adduction of endogenous and food-derived quinones to a protein: its biological significance.Novel biomimetic oxidation of lapachol with H2O2 catalysed by a manganese(iii) porphyrin complexDesign, synthesis and application of fluorescent 2,1,3-benzothiadiazole-triazole-linked biologically active lapachone derivativesOn the investigation of hybrid quinones: synthesis, electrochemical studies and evaluation of trypanocidal activity
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
The trypanocidal activity of naphthoquinones: a review.
@en
The trypanocidal activity of naphthoquinones: a review.
@nl
type
label
The trypanocidal activity of naphthoquinones: a review.
@en
The trypanocidal activity of naphthoquinones: a review.
@nl
prefLabel
The trypanocidal activity of naphthoquinones: a review.
@en
The trypanocidal activity of naphthoquinones: a review.
@nl
P921
P1433
P1476
The trypanocidal activity of naphthoquinones: a review.
@en
P2093
Antônio Ventura Pinto
Solange Lisboa de Castro
P304
P356
10.3390/MOLECULES14114570
P407
P577
2009-11-10T00:00:00Z