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The Constitution of Lapachol and its Derivatives. Part V. The Structure of Paternò's “Isolapachone”1,2
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112713zenodo-depositor-declared
Beta-lapachone: Natural occurrence, physicochemical properties, biological activities, toxicity and synthesis
inferred← citeshttps://doi.org/10.1002/9780470186602.ch13openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cplu.201800485openalex-snapshot
α‐ and β‐Lapachone Isomerization in Acidic Media: Insights from Experimental and Implicit/Explicit Solvation Approaches
inferred← citeshttps://doi.org/10.1002/elan.12023openalex-snapshot
Voltammetric Simultaneous Quantification of Lapachone Isomers In Plant Extracts Using Graphite–Epoxy Composite Electrode
inferred← citeshttps://doi.org/10.1002/oms.1210030703openalex-snapshot
The mass spectra of some naphthoquinones. Lapachol, isolapachol and related compounds
inferred← citeshttps://doi.org/10.1007/s00436-006-0153-8openalex-snapshot
Oxyrane derivative of α-lapachone is potent growth inhibitor of Trypanosoma cruzi epimastigote forms
inferred← citeshttps://doi.org/10.1016/0040-4020(75)80140-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-1-4831-9801-9.50270-1openalex-snapshot
LAPACHOL AND XYLOIDONE
inferred← citeshttps://doi.org/10.1016/j.actatropica.2009.02.008openalex-snapshot
Activities of naphthoquinones against Aedes aegypti (Linnaeus, 1762) (Diptera: Culicidae), vector of dengue and Biomphalaria glabrata (Say, 1818), intermediate host of Schistosoma mansoni
inferred← citeshttps://doi.org/10.1016/j.bmc.2007.10.038openalex-snapshot
Trypanosoma cruzi: Activities of lapachol and α- and β-lapachone derivatives against epimastigote and trypomastigote forms
inferred← citeshttps://doi.org/10.1016/j.bmc.2010.02.032openalex-snapshot
Antiproliferative activity of synthetic naphthoquinones related to lapachol. First synthesis of 5-hydroxylapachol
inferred← citeshttps://doi.org/10.1016/j.bmcl.2003.12.069openalex-snapshot
Antimalarial activity of phenazines from lapachol, β-lapachone and its derivatives against Plasmodium falciparum in vitro and Plasmodium berghei in vivo
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.04.008openalex-snapshot
β-Lapachone analogs with enhanced antiproliferative activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.06.042openalex-snapshot
Biomimetic in vitro oxidation of lapachol: A model to predict and analyse the in vivo phase I metabolism of bioactive compounds
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.02.057openalex-snapshot
QSAR on antiproliferative naphthoquinones based on a conformation-independent approach
inferred← citeshttps://doi.org/10.1016/j.ejps.2021.105861openalex-snapshot
Nanocomposite gels of poloxamine and Laponite for β-Lapachone release in anticancer therapy
inferred← citeshttps://doi.org/10.1016/j.jddst.2019.101292openalex-snapshot
Lapazine loaded Alginate/Chitosan microparticles: Enhancement of anti-mycobacterium activity
inferred← citeshttps://doi.org/10.1016/j.jelechem.2003.10.043openalex-snapshot
Electrochemical studies of isolapachol with emphasis on oxygen interaction with its radical anions
inferred← citeshttps://doi.org/10.1016/j.microc.2013.04.009openalex-snapshot
Improved quantum dots fluorescence quenching using organized medium: A study of the effect of naphthoquinones aiming the analysis of plant extracts
inferred← citeshttps://doi.org/10.1016/j.microc.2017.04.036openalex-snapshot
Voltammetric determination of lapachol in the presence of lapachones and in ethanolic extract of Tabebuia impetiginosa using an epoxy-graphite composite electrode
inferred← citeshttps://doi.org/10.1016/j.phytochem.2005.12.019openalex-snapshot
Newbouldiaquinone A: A naphthoquinone–anthraquinone ether coupled pigment, as a potential antimicrobial and antimalarial agent from Newbouldia laevis
inferred← citeshttps://doi.org/10.1016/j.saa.2012.04.020openalex-snapshot
Determination of lapachol in the presence of other naphthoquinones using 3MPA-CdTe quantum dots fluorescent probe
inferred← citeshttps://doi.org/10.1016/s0001-706x(02)00055-4openalex-snapshot
Toxicity of lapachol and isolapachol and their potassium salts against Biomphalaria glabrata, Schistosoma mansoni cercariae, Artemia salina and Tilapia nilotica
inferred← citeshttps://doi.org/10.1016/s0020-7519(00)00114-4openalex-snapshot
Molluscicidal activity of 2-hydroxy-3-alkyl-1,4-naphthoquinones and derivatives
inferred← citeshttps://doi.org/10.1016/s0021-9673(00)91091-4openalex-snapshot
Tandem high-performance liquid chromatography methods for resolution of lapachol and related naphthaquinones
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)93769-xopenalex-snapshot
Constituents of tabebuia guayacan—II
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)92993-4openalex-snapshot
Synthese des 6-desoxy-cryptosporins
inferred← citeshttps://doi.org/10.1016/s0065-2725(08)60822-3openalex-snapshot
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CDC Reaction and Subsequent Cyclization for the Synthesis of 2-Hydroxy-3-alkyl-1,4-naphthoquinones and Pyranonaphthoquinones
inferred← citeshttps://doi.org/10.1021/jacs.5c21759openalex-snapshot
A Hooker Oxygenase Archetype in Polyketide Biosynthesis Challenging the Baeyer–Villiger Monooxygenase Paradigm
inferred← citeshttps://doi.org/10.1021/je400725nopenalex-snapshot
Thermodynamic Parameters of the Interactions between Lapachol and Isolapachol Sodium Salts and Chitosan Flakes
inferred← citeshttps://doi.org/10.1039/b810413aopenalex-snapshot
Characterization, reactivity and photosensitizing properties of the triplet excited state of α-lapachone
inferred← citeshttps://doi.org/10.1039/c4ob01869aopenalex-snapshot
Novel naphthoquinone derivatives and evaluation of their trypanocidal and leishmanicidal activities
inferred← citeshttps://doi.org/10.1039/c6ra14701aopenalex-snapshot
Fluorescent oxazoles from quinones for bioimaging applications
inferred← citeshttps://doi.org/10.1039/c8nj03699copenalex-snapshot
An efficient cyclization of lapachol to new benzo[ h ]chromene hybrid compounds: a stepwise vs. one-pot esterification-click (CuAAC) study
inferred← citeshttps://doi.org/10.1039/d0ra05717gopenalex-snapshot
Mannich bases derived from lawsone and their metal complexes: synthetic strategies and biological properties
inferred← citeshttps://doi.org/10.1039/d2sc05377bopenalex-snapshot
A bioinspired, one-step total synthesis of peshawaraquinone
inferred← citeshttps://doi.org/10.1111/j.2042-7158.2011.01323.xopenalex-snapshot
Light effect on the stability of β -lapachone in solution: pathways and kinetics of degradation
inferred← citeshttps://doi.org/10.1128/aem.38.2.311-313.1979openalex-snapshot
Microbial transformations of natural antitumor agents: conversion of lapachol to dehydro-alpha-lapachone by Curvularia lunata
inferred← citeshttps://doi.org/10.1155/2015/812701openalex-snapshot
Development and Validation of a Simple and Selective Analytical HPLC Method for the Quantification of Oxaliplatin
inferred← citeshttps://doi.org/10.1208/pt0803060openalex-snapshot
Characterization of β-lapachone and methylated β-cyclodextrin solid-state systems
inferred← citeshttps://doi.org/10.1515/bchm2.1941.268.3-4.85openalex-snapshot
Über einige neue Oxydationsprodukte der Tokopherole. 8. Mitteilung über Antisterilitätsfaktoren (Vitamin E)
inferred← citeshttps://doi.org/10.1590/0074-0276130603openalex-snapshot
Blood shizonticidal activities of phenazines and naphthoquinoidal compounds against Plasmodium falciparum in vitro and in mice malaria studies
inferred← citeshttps://doi.org/10.1590/s0074-02762004000700017openalex-snapshot
Antileishmanial activity of lapachol analogues
inferred← citeshttps://doi.org/10.1590/s0102-695x2008000200007openalex-snapshot
Spasmolytic activity of lapachol and its derivatives, α and β-lapachone, on the guinea-pig ileum involves blockade of voltage-gated calcium channels
inferred← citeshttps://doi.org/10.1590/s0104-66322003000300011openalex-snapshot
Extraction of lapachol from Tabebuia avellanedae wood with supercritical CO2: an alternative to Soxhlet extraction?
inferred← citeshttps://doi.org/10.3109/03639048509057698openalex-snapshot
Some Formulation Properties of Lapachol, A Potential Oncolytic Agent of Natural Origin
inferred← citeshttps://doi.org/10.3390/ph17101375openalex-snapshot
Exploring Benzo[h]chromene Derivatives as Agents against Protozoal and Mycobacterial Infections
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