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Synthesis, Characterization, and Antileukemic Properties of Naphthoquinone Derivatives of Lawsone

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Anti-Inflammatory and Anticancer Drugs from Nature
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A microtiter plate assay for total glutathione and glutathione disulfide contents in cultured/isolated cells: performance study of a new miniaturized protocol
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Effects of β-lapachone, a new anticancer candidate, on cytochrome P450-mediated drug metabolism
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Molecular mechanisms of quinone cytotoxicity
inferredcites →https://doi.org/10.1016/0031-9422(73)80710-1openalex-snapshot
Quinones and other constituents from Tabebuia rosea
inferredcites →https://doi.org/10.1016/0031-9422(75)83039-1openalex-snapshot
Binaphthoquinones in Lomatia ferruginea
inferredcites →https://doi.org/10.1016/0031-9422(88)83017-6openalex-snapshot
Isolation and cytotoxicity of rhinacanthin-A and -B, two; naphthoquinones, from Rhinacanthus nasutus
inferredcites →https://doi.org/10.1016/0041-008x(92)90273-uopenalex-snapshot
Quinone chemistry and toxicity
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Trypanosoma cruzi: Activities of lapachol and α- and β-lapachone derivatives against epimastigote and trypomastigote forms
inferredcites →https://doi.org/10.1016/j.bmc.2011.10.005openalex-snapshot
Metabolic and electrochemical mechanisms of dimeric naphthoquinones cytotoxicity in breast cancer cells
inferredcites →https://doi.org/10.1016/j.bmcl.2014.07.022openalex-snapshot
Phytochemical analysis and antileukemic activity of polyphenolic constituents of Toona sinensis
inferredcites →https://doi.org/10.1016/j.ejmech.2007.12.023openalex-snapshot
Studies of trypanocidal (inhibitory) power of naphthoquinones: Evaluation of quantum chemical molecular descriptors for structure–activity relationships
inferredcites →https://doi.org/10.1016/j.intimp.2006.12.006openalex-snapshot
Anti-inflammatory effects of β-lapachone in lipopolysaccharide-stimulated BV2 microglia
inferredcites →https://doi.org/10.1016/j.phymed.2013.08.010openalex-snapshot
β-Lapachone activity in synergy with conventional antimicrobials against methicillin resistant Staphylococcus aureus strains
inferredcites →https://doi.org/10.1016/j.tetlet.2009.01.058openalex-snapshot
Unexpected transformation of quinones to spirolactones and to naturally occurring naphthalenic compounds
inferredcites →https://doi.org/10.1016/s0006-2952(00)00437-8openalex-snapshot
Novel mechanisms of DNA topoisomerase II inhibition by pyranonaphthoquinone derivatives—eleutherin, α lapachone, and β lapachone∗
inferredcites →https://doi.org/10.1016/s0031-9422(00)86973-3openalex-snapshot
Quinones of streptocarpus dunnii
inferredcites →https://doi.org/10.1016/s0040-4039(98)01880-2openalex-snapshot
A preparative synthesis of lapachol and related naphthoquinones
inferredcites →https://doi.org/10.1016/s0924-8579(02)00349-7openalex-snapshot
In vitro activity of Brazilian medicinal plants, naturally occurring naphthoquinones and their analogues, against methicillin-resistant Staphylococcus aureus
inferredcites →https://doi.org/10.1021/jf980769jopenalex-snapshot
Isolation, Characterization, and Biological Activity of Naphthoquinones fromCalceolaria andinaL.
inferredcites →https://doi.org/10.1021/jm00158a010openalex-snapshot
One-electron reduction of 2- and 6-methyl-1,4-naphthoquinone bioreductive alkylating agents
inferredcites →https://doi.org/10.1021/mp300296mopenalex-snapshot
Metabolic Profile, Enzyme Kinetics, and Reaction Phenotyping of β-Lapachone Metabolism in Human Liver and Intestine in Vitro
inferredcites →https://doi.org/10.1021/np068004qopenalex-snapshot
Constituents of the Root Wood of Austroplenckia populnea var. ovata
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Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010
inferredcites →https://doi.org/10.1038/sj.embor.7400645openalex-snapshot
The role of glutathione in disulphide bond formation and endoplasmic‐reticulum‐generated oxidative stress
inferredcites →https://doi.org/10.1039/j39670002100openalex-snapshot
Naturally occurring quinones. Part X. The quinonoid constituents of Tabebuia avellanedae(Bignoniaceae)
inferredcites →https://doi.org/10.1039/j39680000850openalex-snapshot
Naturally occurring quinones. Part XII. Extractives from Tabebuia chrysantha nichols and other bignoniaceae
inferredcites →https://doi.org/10.1055/s-0032-1317541openalex-snapshot
Synthesis of Hemitectol, Tectol, and Tecomaquinone I
inferredcites →https://doi.org/10.1055/s-2006-959504openalex-snapshot
Comparison of Antibacterial and Antifungal Activities of Lapachol and β-Lapachone
inferredcites →https://doi.org/10.1071/ch9731121openalex-snapshot
Chemical Studies of the Proteaceae. VI Two Naphthoquinones From Stenocarpus salignus
inferredcites →https://doi.org/10.1073/pnas.0538044100openalex-snapshot
Selective killing of cancer cells by β-lapachone: Direct checkpoint activation as a strategy against cancer
inferredcites →https://doi.org/10.1248/cpb.c13-00011openalex-snapshot
Synthesis and Cytotoxicity on Human Leukemia Cells of Furonaphthoquinones Isolated from Tabebuia Plants
inferredcites →https://doi.org/10.2174/092986711793979779openalex-snapshot
Natural and Synthetic Naphthoquinones Active Against Trypanosoma Cruzi: An Initial Step Towards New Drugs for Chagas Disease
inferredcites →https://doi.org/10.2174/1568009023333854openalex-snapshot
Cancer Therapy with ß-Lapachone
inferredcites →https://doi.org/10.3390/molecules14114570openalex-snapshot
The Trypanocidal Activity of Naphthoquinones: A Review
inferredcites →https://doi.org/10.3998/ark.5550190.0008.204openalex-snapshot
Lapachol: An overview
inferredcites →https://doi.org/10.5012/bkcs.2011.32.1.153openalex-snapshot
Concise Synthesis of (±)-Rhinacanthin A, Dehydro α-Lapachone, and β-Lapachone, and Pyranonaphthoquinone Derivatives

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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ChemInform Abstract: Synthesis, Characterization, and Antileukemic Properties of Naphthoquinone Derivatives of Lawsone.
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Synthesis of Lapachone Derivates via Ionic Liquid‐Mediated Tandem Knoevenagel/Diels‐Alder Reaction
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Novel pyrrolidine-aminophenyl-1,4-naphthoquinones: structure-related mechanisms of leukemia cell death
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A green approach for synthesis of naphthoquinone-fused oxazine derivatives in water under ultrasonic irradiation
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Synthesis of carbazoloquinone derivatives and their antileukemic activity via modulating cellular reactive oxygen species
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Comparative Analysis of p-Terphenylquinone and Seriniquinone Derivatives as Reactive Oxygen Species-Modulating Agents
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Pd-catalyzed regioselective hydroesterification of 3-allyl-2-hydroxynaphthoquinones: Easy access to linear or branched naphthoquinone esters
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Extracellular production of tellurium nanoparticles by the photosynthetic bacterium Rhodobacter capsulatus
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Bislawsone as a robust redox mediator for high-performance aqueous polysulfide redox flow batteries
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Low melting oxalic acid/proline mixture as dual solvent/catalyst for efficient synthesis of 13-aryl-13 H -benzo[ g ]benzothiazolo[2,3- b ]buinazoline-5,4-diones under microwave irradiation
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Synthesis, structural characterization, and computational evaluation of a pyrazolo[3,4-b]quinolinedione derivative as a potential dual inhibitor of DNA Gyrase and KPC-2 carbapenemase
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Synthesis, characterization and antiproliferative activity of mixed ligand complexes of Cu2+ and Co2+ with lapachol
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Trichomes and naphthoquinones protect Streptocarpus dunnii Hook.f. against environmental stresses
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Effects of (±)-dunnione and quinone-containing extracts from in vitro-cultured plantlets of Streptocarpus dunnii Hook. f. and a hybrid ‘Ruby’ on seed germination
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Lapachol acetylglycosylation enhances its cytotoxic and pro-apoptotic activities in HL60 cells
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Tridentate 3-Substituted Naphthoquinone Ruthenium Arene Complexes: Synthesis, Characterization, Aqueous Behavior, and Theoretical and Biological Studies
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A Photoactivatable Probe for Super-Resolution Imaging of Enzymatic Activity in Live Cells
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A common tattoo chemical for energy storage: henna plant-derived naphthoquinone dimer as a green and sustainable cathode material for Li-ion batteries
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p -TsOH promoted synthesis of benzo-fused O-heterocycles from alkynols via ring contraction and C–O scission strategy
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Site-selectivity control in hetero-Diels–Alder reactions of methylidene derivatives of lawsone through modification of the reactive carbonyl group: an experimental and theoretical study
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Synthesis of fused 1,2-naphthoquinones with cytotoxic activity using a one-pot three-step reaction
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Bidirectional noninnocence of hinge-like deprotonated bis-lawsone on selective ruthenium platform: a function of varying ancillary ligands
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A bioinspired, one-step total synthesis of peshawaraquinone
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In vitro anticancer evaluation of Enceleamycin A and its underlying mechanism
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β-lapachone regulates mammalian inositol pyrophosphate levels in an NQO1- and oxygen-dependent manner
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Two new naphthoquinone derivatives from Sinningia conspicua (Gesneriaceae)
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β-Lapachone Regulates Mammalian Inositol Pyrophosphate Levels in an NQO1- and Oxygen-dependent Manner
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Lawsone (2-hydroxy-1,4-naphthaquinone) derived anticancer agents
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Molecular Docking and Quantum Studies of Lawsone Dimers Derivatives: New Investigation of Antioxidant Behavior and Antifungal Activity
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Síntese do fármaco ß-lapachona e seus derivados: uma nova abordagem
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Analysis of the Mechanisms of Action of Naphthoquinone-Based Anti-Acute Myeloid Leukemia Chemotherapeutics
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Identification of HIV-1 Reverse Transcriptase-Associated Ribonuclease H Inhibitors Based on 2-Hydroxy-1,4-naphthoquinone Mannich Bases
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Construction of Cyclic Ether-Fused Tricyclic Naphthoquinone Derivatives by Intramolecular Cyclization Reaction
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LAWSONE FROM LAWSONIA INERMIS: ISOLATION AND PHARMACOLOGICAL ACTIVITIES
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Synthesis of 1,2-naphthoquinone derivatives as α-glucosidase inhibitors
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Novel N,S-Substituted naphthoquinone analogues from aminonaphthoquinones
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