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Efficient NQO1 Substrates are Potent and Selective Anticancer Agents
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ijc.2910450304openalex-snapshot
Cytosolic NAD(P)H:(Quinone‐acceptor)oxidoreductase in human normal and tumor tissue: Effects of cigarette smoking and alcohol
inferredcites →https://doi.org/10.1002/ijc.2910560124openalex-snapshot
Unusually marked hypoxic sensitization to indoloquinone E09 and mitomycin C in a human colon‐tumour cell line that lacks DT‐diaphorase activity
inferredcites →https://doi.org/10.1002/mc.20107openalex-snapshot
Targeting NAD(P)H:quinone oxidoreductase (NQO1) in pancreatic cancer
inferredcites →https://doi.org/10.1002/mc.20199openalex-snapshot
Targeting NAD(P)H:Quinone Oxidoreductase (NQO1) in Pancreatic Cancer
inferredcites →https://doi.org/10.1006/abbi.1997.0340openalex-snapshot
Comparison of Oxygen Radical Generation from the Reductive Activation of Doxorubicin, Streptonigrin, and Menadione by Xanthine Oxidase and Xanthine Dehydrogenase
inferredcites →https://doi.org/10.1007/978-0-387-77300-1openalex-snapshot
Advances in Bioactivation Research
inferredcites →https://doi.org/10.1007/s00018-007-7300-yopenalex-snapshot
Flavin-dependent quinone reductases
inferredcites →https://doi.org/10.1016/0360-3016(94)90278-xopenalex-snapshot
Relative importance of DT-diaphorase and hypoxia in the bioactivation of e09 by human lung tumor cell lines
inferredcites →https://doi.org/10.1016/0959-8049(92)90049-8openalex-snapshot
DT-diaphorase activity correlates with sensitivity to the indoloquinone EO9 in mouse and human colon carcinomas
inferredcites →https://doi.org/10.1016/j.bcp.2011.12.017openalex-snapshot
NAD(P)H:quinone oxidoreductase 1 (NQO1) in the sensitivity and resistance to antitumor quinones
inferredcites →https://doi.org/10.1016/j.cbi.2010.04.022openalex-snapshot
ES936 stimulates DNA synthesis in HeLa cells independently on NAD(P)H:quinone oxidoreductase 1 inhibition, through a mechanism involving p38 MAPK
inferredcites →https://doi.org/10.1016/j.ctrv.2004.01.002openalex-snapshot
DT-diaphorase: a target for new anticancer drugs
inferredcites →https://doi.org/10.1016/s0003-9861(03)00281-9openalex-snapshot
Cytotoxicity of RH1 and related aziridinylbenzoquinones: involvement of activation by NAD(P)H:quinone oxidoreductase (NQO1) and oxidative stress
inferredcites →https://doi.org/10.1016/s0006-2952(02)01383-7openalex-snapshot
A physiological threshold for protection against menadione toxicity by human NAD(P)H:quinone oxidoreductase (NQO1) in Chinese hamster ovary (CHO) cells
inferredcites →https://doi.org/10.1016/s0006-2952(95)00223-5openalex-snapshot
Role of NAD(P)H:Quinone oxidoreductase (DT-diaphorase) in cytotoxicity and induction of DNA damage by streptonigrin
inferredcites →https://doi.org/10.1016/s0021-9258(19)42173-xopenalex-snapshot
Properties and Reaction Mechanism of DT Diaphorase from Rat Liver
inferredcites →https://doi.org/10.1016/s0076-6879(04)82018-4openalex-snapshot
Induction of NQO1 in Cancer Cells
inferredcites →https://doi.org/10.1016/s0891-5849(00)00314-2openalex-snapshot
The role of NAD(P)H oxidoreductase (DT-Diaphorase) in the bioactivation of quinone-containing antitumor agents: a review
inferredcites →https://doi.org/10.1016/s0969-2126(01)00636-0openalex-snapshot
Structure-Based Development of Anticancer Drugs
inferredcites →https://doi.org/10.1021/bi00149a019openalex-snapshot
Bioreductive activation of mitomycin C by DT-diaphorase
inferredcites →https://doi.org/10.1021/bi011324iopenalex-snapshot
Characterization of a Mechanism-Based Inhibitor of NAD(P)H:Quinone Oxidoreductase 1 by Biochemical, X-ray Crystallographic, and Mass Spectrometric Approaches
inferredcites →https://doi.org/10.1021/bi0600087openalex-snapshot
The Crystal Structure of NAD(P)H Quinone Oxidoreductase 1 in Complex with Its Potent Inhibitor Dicoumarol
inferredcites →https://doi.org/10.1021/bi300760uopenalex-snapshot
Human NAD(P)H:Quinone Oxidoreductase Type I (hNQO1) Activation of Quinone Propionic Acid Trigger Groups
inferredcites →https://doi.org/10.1021/ja100610mopenalex-snapshot
Chemistry and Biology of Deoxynyboquinone, a Potent Inducer of Cancer Cell Death
inferredcites →https://doi.org/10.1038/bjc.1967.32openalex-snapshot
A trial of streptonigrin in the treatment of advanced malignant disease.
inferredcites →https://doi.org/10.1038/bjc.1994.461openalex-snapshot
DT-diaphorase protects cells from the hypoxic cytotoxicity of indoloquinone EO9
inferredcites →https://doi.org/10.1038/bjc.1995.433openalex-snapshot
DT-diaphorase activity in normal and neoplastic human tissues; an indicator for sensitivity to bioreductive agents?
inferredcites →https://doi.org/10.1038/bjc.1997.474openalex-snapshot
Ethnic variation in the prevalence of a common NAD(P)H quinone oxidoreductase polymorphism and its implications for anti-cancer chemotherapy
inferredcites →https://doi.org/10.1038/bjc.1997.485openalex-snapshot
DT-diaphorase and cytochrome B5 reductase in human lung and breast tumours
inferredcites →https://doi.org/10.1038/nprot.2006.179openalex-snapshot
Sulforhodamine B colorimetric assay for cytotoxicity screening
inferredcites →https://doi.org/10.1038/sj.bjp.0704916openalex-snapshot
Pharmacological approach towards the development of indolequinone bioreductive drugs based on the clinically inactive agent EO9
inferredcites →https://doi.org/10.1073/pnas.0702176104openalex-snapshot
An NQO1- and PARP-1-mediated cell death pathway induced in non-small-cell lung cancer cells by β-lapachone
inferredcites →https://doi.org/10.1073/pnas.92.19.8846openalex-snapshot
The three-dimensional structure of NAD(P)H:quinone reductase, a flavoprotein involved in cancer chemoprotection and chemotherapy: mechanism of the two-electron reduction.
inferredcites →https://doi.org/10.1073/pnas.97.7.3177openalex-snapshot
Structures of recombinant human and mouse NAD(P)H:quinone oxidoreductases: Species comparison and structural changes with substrate binding and release
inferredcites →https://doi.org/10.1074/jbc.275.8.5416openalex-snapshot
NAD(P)H:Quinone Oxidoreductase Activity Is the Principal Determinant of β-Lapachone Cytotoxicity
inferredcites →https://doi.org/10.1080/10715760600833077openalex-snapshot
The reductive activation of the antitumor drug RH1 to its semiquinone free radical by NADPH cytochrome P450 reductase and by HCT116 human colon cancer cells
inferredcites →https://doi.org/10.1093/annonc/mdq638openalex-snapshot
Phase I pharmacokinetic and pharmacodynamic study of the bioreductive drug RH1
inferredcites →https://doi.org/10.1093/jnci/88.5.259openalex-snapshot
Reductase Enzyme Expression Across the National Cancer Institute Tumor Cell Line Panel: Correlation With Sensitivity to Mitomycin C and EO9
inferredcites →https://doi.org/10.1093/jnci/93.15.1166openalex-snapshot
NAD(P)H : quinone Oxidoreductase 1 Deficiency and Increased Susceptibility to 7,12-Dimethylbenz[a]-anthracene-Induced Carcinogenesis in Mouse Skin
inferredcites →https://doi.org/10.1097/00001813-200504000-00004openalex-snapshot
Cytotoxicity of RH1: NAD(P)H:quinone acceptor oxidoreductase (NQO1)-independent oxidative stress and apoptosis induction
inferredcites →https://doi.org/10.1097/pai.0b013e31802e91d0openalex-snapshot
NQO1 Expression in Pancreatic Cancer and Its Potential Use as a Biomarker
inferredcites →https://doi.org/10.1124/dmd.107.018572openalex-snapshot
Identification of the in Vitro Metabolites of 3,4-Dihydro-2,2-dimethyl-2H-naphthol[1,2-b ]pyran-5,6-dione (ARQ 501; β-Lapachone) in Whole Blood
inferredcites →https://doi.org/10.1124/dmd.108.022004openalex-snapshot
Enzymatic Reduction and Glutathione Conjugation of Benzoquinone Ansamycin Heat Shock Protein 90 Inhibitors: Relevance for Toxicity and Mechanism of Action
inferredcites →https://doi.org/10.1124/jpet.104.081380openalex-snapshot
RH1 Induces Cellular Damage in an NAD(P)H:Quinone Oxidoreductase 1-Dependent Manner: Relationship between DNA Cross-linking, Cell Cycle Perturbations, and Apoptosis
inferredcites →https://doi.org/10.1124/mol.108.050401openalex-snapshot
Dissecting the Role of Multiple Reductases in Bioactivation and Cytotoxicity of the Antitumor Agent 2,5-Diaziridinyl-3-(hydroxymethyl)-6-methyl-1,4-benzoquinone (RH1)
inferredcites →https://doi.org/10.1124/mol.109.055855openalex-snapshot
Potent Activity of Indolequinones against Human Pancreatic Cancer: Identification of Thioredoxin Reductase as a Potential Target
inferredcites →https://doi.org/10.1124/mol.64.3.714openalex-snapshot
Biochemical, Cytotoxic, and Genotoxic Effects of ES936, a Mechanism-Based Inhibitor of NAD(P)H:quinone Oxidoreductase 1, in Cellular Systems
inferredcites →https://doi.org/10.1124/mol.65.5.1238openalex-snapshot
NAD(P)H:Quinone Oxidoreductase 1: Role as a Superoxide Scavenger
inferredcites →https://doi.org/10.1158/0008-5472.can-11-3135openalex-snapshot
An NQO1 Substrate with Potent Antitumor Activity That Selectively Kills by PARP1-Induced Programmed Necrosis
inferredcites →https://doi.org/10.1158/1078-0432.ccr-03-0411openalex-snapshot
Development of a New Isogenic Cell-Xenograft System for Evaluation of NAD(P)H:Quinone Oxidoreductase-Directed Antitumor Quinones
inferredcites →https://doi.org/10.1158/1078-0432.ccr-10-1983openalex-snapshot
Modulating Endogenous NQO1 Levels Identifies Key Regulatory Mechanisms of Action of β-Lapachone for Pancreatic Cancer Therapy
inferredcites →https://doi.org/10.1515/bchm3.1994.375.7.439openalex-snapshot
Loss of Heterozygosity at the NAD(P)H:Quinone Oxidoreductase Locus Associated with Increased Resistance against Mitomycin C in a Human Bladder Carcinoma Cell Line
inferredcites →https://doi.org/10.2174/156802608786786624openalex-snapshot
Medicinal Chemistry and the Molecular Operating Environment (MOE): Application of QSAR and Molecular Docking to Drug Discovery
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/bkcs.12137openalex-snapshot
Trimethyl Lock Quinone‐Functionalized Coumarin for Real‐time Monitoring of NQO1 Activity in the Live Cells
inferred← citeshttps://doi.org/10.1002/cctc.202401609openalex-snapshot
Recent Advances in the Development of Targeted Activation Strategies for Organoboron Prodrugs
inferred← citeshttps://doi.org/10.1002/ejoc.201403064openalex-snapshot
Synthesis of β‐Lapachone, a Potential Anticancer Agent from the Lapacho Tree
inferred← citeshttps://doi.org/10.1007/978-981-15-6815-2_9openalex-snapshot
Computational Screening Techniques for Lead Design and Development
inferred← citeshttps://doi.org/10.1007/s10637-016-0414-zopenalex-snapshot
Pharmacokinetics and derivation of an anticancer dosing regimen for the novel anti-cancer agent isobutyl-deoxynyboquinone (IB-DNQ), a NQO1 bioactivatable molecule, in the domestic felid species
inferred← citeshttps://doi.org/10.1007/s12032-017-1011-5openalex-snapshot
Molecular modeling and structure-based drug discovery approach reveals protein kinases as off-targets for novel anticancer drug RH1
inferred← citeshttps://doi.org/10.1016/b978-0-12-420117-0.00008-6openalex-snapshot
Role of the Keap1–Nrf2 Pathway in Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00084-6openalex-snapshot
Tricyclic systems: Central Carbon Ring With Fused Six-Membered Rings
inferred← citeshttps://doi.org/10.1016/j.bbapap.2015.11.005openalex-snapshot
Quantitative proteomic analysis of anticancer drug RH1 resistance in liver carcinoma
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.12.082openalex-snapshot
Distinct responses of compartmentalized glutathione redox potentials to pharmacologic quinones targeting NQO1
inferred← citeshttps://doi.org/10.1016/j.bioelechem.2014.03.012openalex-snapshot
Information processing through a bio-based redox capacitor: Signatures for redox-cycling
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104995openalex-snapshot
Design, synthesis, and biological evaluation of 3-(1-benzotriazole)-nor-β-lapachones as NQO1-directed antitumor agents
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106385openalex-snapshot
Design, synthesis, and biological evaluation of quinolinedione-linked sulfonylpiperazine derivatives as NQO1-directed antitumor agents
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107509openalex-snapshot
Dual-targeted NAMPT inhibitors as a progressive strategy for cancer therapy
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.110146openalex-snapshot
Discovery of novel NQO1/STAT3/HDAC triple-target agents for the treatment of triple negative breast cancer
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.01.024openalex-snapshot
Novel naphtho[2,1-d]oxazole-4,5-diones as NQO1 substrates with improved aqueous solubility: Design, synthesis, and in vivo antitumor evaluation
inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.128992openalex-snapshot
Comparative Analysis of p-Terphenylquinone and Seriniquinone Derivatives as Reactive Oxygen Species-Modulating Agents
inferred← citeshttps://doi.org/10.1016/j.cbi.2021.109574openalex-snapshot
Interactions of the antioxidant enzymes NAD(P)H: Quinone oxidoreductase 1 (NQO1) and NRH: Quinone oxidoreductase 2 (NQO2) with pharmacological agents, endogenous biochemicals and environmental contaminants
inferred← citeshttps://doi.org/10.1016/j.cell.2022.04.014openalex-snapshot
Systematic discovery of mutation-directed neo-protein-protein interactions in cancer
inferred← citeshttps://doi.org/10.1016/j.drudis.2016.02.004openalex-snapshot
Filtering promiscuous compounds in early drug discovery: is it a good idea?
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.05.041openalex-snapshot
2-Substituted 3-methylnaphtho[1,2-b]furan-4,5-diones as novel L-shaped ortho-quinone substrates for NAD(P)H:quinone oxidoreductase (NQO1)
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.02.004openalex-snapshot
Discovery of quinone-directed antitumor agents selectively bioactivated by NQO1 over CPR with improved safety profile
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.03.055openalex-snapshot
Design, synthesis, and biological evaluation of NAD(P)H: Quinone oxidoreductase (NQO1)-targeted oridonin prodrugs possessing indolequinone moiety for hypoxia-selective activation
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.06.056openalex-snapshot
Synthesis of quinones with highlighted biological applications: A critical update on the strategies towards bioactive compounds with emphasis on lapachones
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112274openalex-snapshot
Hypoxia-activated nanomedicines for effective cancer therapy
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112396openalex-snapshot
Design, synthesis, and biological evaluation of 4-substituted-3,4-dihydrobenzo[h]quinoline-2,5,6(1H)-triones as NQO1-directed antitumor agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113515openalex-snapshot
Application of cation-π interactions in enzyme-substrate binding: Design, synthesis, biological evaluation, and molecular dynamics insights of novel hydrophilic substrates for NQO1
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116448openalex-snapshot
Exploration of novel isoxazole-fused quinone derivatives as anti-colorectal cancer agents through inhibiting STAT3 and elevating ROS level
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117377openalex-snapshot
Discovery of naphthoquinone-furo-piperidone derivatives as dual targeting agents of STAT3 and NQO1 for the treatment of breast cancer
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2018.11.018openalex-snapshot
A promising redox cycle-based strategy for designing a catechol-type diphenylbutadiene as a potent prooxidative anti-melanoma agent
inferred← citeshttps://doi.org/10.1016/j.jconrel.2022.05.031openalex-snapshot
Bladder cancer selective chemotherapy with potent NQO1 substrate co-loaded prodrug nanoparticles
inferred← citeshttps://doi.org/10.1016/j.neo.2021.06.008openalex-snapshot
Utilizing feline oral squamous cell carcinoma patients to develop NQO1-targeted therapy
inferred← citeshttps://doi.org/10.1016/j.phymed.2019.153133openalex-snapshot
NADPH: Quinone oxidoreductase 1 (NQO1) mediated anti-cancer effects of plumbagin in endocrine resistant MCF7 breast cancer cells
inferred← citeshttps://doi.org/10.1016/j.snb.2020.128557openalex-snapshot
Electrochemiluminescent detection of hNQO1 and associated drug screening enabled by futile redox cycle reaction
inferred← citeshttps://doi.org/10.1021/acs.accounts.5b00365openalex-snapshot
Deoxynyboquinones as NQO1-Activated Cancer Therapeutics
inferred← citeshttps://doi.org/10.1021/acs.chemrestox.5b00336openalex-snapshot
Study of Bioreductive Anticancer Agent RH-1-Induced Signals Leading the Wild-Type p53-Bearing Lung Cancer A549 Cells to Apoptosis
inferred← citeshttps://doi.org/10.1021/acs.jchemed.3c00307openalex-snapshot
Design and Implementation of an Accessible and Open-Sourced In Silico Drug Screening Activity for Cancer Drug Discovery
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c00077openalex-snapshot
Discovery of Small Molecules Simultaneously Targeting NAD(P)H:Quinone Oxidoreductase 1 and Nicotinamide Phosphoribosyltransferase: Treatment of Drug-Resistant Non-small-Cell Lung Cancer
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b01243openalex-snapshot
Role of Reactive Oxygen Species (ROS) in Therapeutics and Drug Resistance in Cancer and Bacteria
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.8b00124openalex-snapshot
NAD(P)H:Quinone Oxidoreductase 1 (NQO1) as a Therapeutic and Diagnostic Target in Cancer
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.8b01424openalex-snapshot
Discovery of Nonquinone Substrates for NAD(P)H: Quinone Oxidoreductase 1 (NQO1) as Effective Intracellular ROS Generators for the Treatment of Drug-Resistant Non-Small-Cell Lung Cancer
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01028openalex-snapshot
Diazaquinomycin Biosynthetic Gene Clusters from Marine and Freshwater Actinomycetes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01015openalex-snapshot
Structure Determination, Functional Characterization, and Biosynthetic Implications of Nybomycin Metabolites from a Mining Reclamation Site-Associated Streptomyces
inferred← citeshttps://doi.org/10.1021/acs.joc.5c03182openalex-snapshot
Free-Radical-Promoted β-C-H Functionalization of Simple Aliphatic Ketones, Esters, and Acids with Quinones
inferred← citeshttps://doi.org/10.1021/acs.macromol.1c01049openalex-snapshot
Polyaddition Synthesis Using Alkyne Esters for the Design of Vinylogous Urethane Vitrimers
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01304openalex-snapshot
Palladium(II)-Catalyzed C–H Bond Activation/C–C Coupling/Intramolecular Tsuji–Trost Reaction Cascade: Facile Access to 2H-Pyranonaphthoquinones
inferred← citeshttps://doi.org/10.1021/acsami.1c13634openalex-snapshot
Strategic Design of Intelligent-Responsive Nanogel Carriers for Cancer Therapy
inferred← citeshttps://doi.org/10.1021/acschembio.7b00015openalex-snapshot
Reactive Oxygen Species Synergize To Potently and Selectively Induce Cancer Cell Death
inferred← citeshttps://doi.org/10.1021/acsinfecdis.9b00413openalex-snapshot
Instructive Advances in Chemical Microbiology Inspired by Nature’s Diverse Inventory of Molecules
inferred← citeshttps://doi.org/10.1021/acssensors.1c00365openalex-snapshot
Detecting Attomolar DNA-Damaging Anticancer Drug Activity in Cell Lysates with Electrochemical DNA Devices
inferred← citeshttps://doi.org/10.1021/ml5001118openalex-snapshot
Bioreductively Activated Reactive Oxygen Species (ROS) Generators as MRSA Inhibitors
inferred← citeshttps://doi.org/10.1038/ncomms7947openalex-snapshot
Deoxynybomycins inhibit mutant DNA gyrase and rescue mice infected with fluoroquinolone-resistant bacteria
inferred← citeshttps://doi.org/10.1038/s41401-023-01052-3openalex-snapshot
Skullcapflavone II, a novel NQO1 inhibitor, alleviates aristolochic acid I-induced liver and kidney injury in mice
inferred← citeshttps://doi.org/10.1038/s41557-019-0261-6openalex-snapshot
Diverse compounds from pleuromutilin lead to a thioredoxin inhibitor and inducer of ferroptosis
inferred← citeshttps://doi.org/10.1039/c5ra05919dopenalex-snapshot
Discovery of NAD(P)H:quinone oxidoreductase 1 (NQO1) inhibitors with novel chemical scaffolds by shape-based virtual screening combined with cascade docking
inferred← citeshttps://doi.org/10.1039/c8ra09792eopenalex-snapshot
Total synthesis of diazaquinomycins H and J using double Knorr cyclization in the presence of triisopropylsilane
inferred← citeshttps://doi.org/10.1039/c9md00207copenalex-snapshot
Synthetic studies on the reverse antibiotic natural products, the nybomycins
inferred← citeshttps://doi.org/10.1042/bsr20191874openalex-snapshot
Cancer-associated variants of human NQO1: impacts on inhibitor binding and cooperativity
inferred← citeshttps://doi.org/10.1089/ars.2022.0224openalex-snapshot
Isopentyl-Deoxynboquinone Induces Mitochondrial Dysfunction and G2/M Phase Cell Cycle Arrest to Selectively Kill NQO1 -Positive Pancreatic Cancer Cells
inferred← citeshttps://doi.org/10.1093/toxres/tfae123openalex-snapshot
Study on the mechanism of hepatotoxicity of Aucklandiae radix through liver metabolomics and network pharmacology
inferred← citeshttps://doi.org/10.1101/2024.05.15.594427openalex-snapshot
Unraveling systemic responses to NQO1-activated IB-DNQ and Rucaparib single and dual agent therapy in triple-negative breast cancers
inferred← citeshttps://doi.org/10.1111/cbdd.13051openalex-snapshot
Combined molecular modelling and 3D‐QSAR study for understanding the inhibition of NQO1 by heterocyclic quinone derivatives
inferred← citeshttps://doi.org/10.1111/cbdd.13752openalex-snapshot
Novel β‐carboline‐based indole‐4,7‐quinone derivatives as NAD(P)H: Quinone‐oxidoreductase‐1 inhibitor with potent antitumor activities by inducing reactive oxygen species, apoptosis, and DNA damage
inferred← citeshttps://doi.org/10.18388/abp.2014_1854openalex-snapshot
Cytotoxicity of anticancer aziridinyl-substituted benzoquinones in primary mice splenocytes.
inferred← citeshttps://doi.org/10.2147/ijn.s196959openalex-snapshot
Hypoxia-active nanoparticles used in tumor theranostic
inferred← citeshttps://doi.org/10.3390/cancers15245844openalex-snapshot
Augmented Concentration of Isopentyl-Deoxynyboquinone in Tumors Selectively Kills NAD(P)H Quinone Oxidoreductase 1-Positive Cancer Cells through Programmed Necrotic and Apoptotic Mechanisms
inferred← citeshttps://doi.org/10.3390/molecules24224115openalex-snapshot
5,8-Quinolinedione Scaffold as a Promising Moiety of Bioactive Agents
inferred← citeshttps://doi.org/10.3390/molecules28135202openalex-snapshot
Heterocyclic Iminoquinones and Quinones from the National Cancer Institute (NCI, USA) COMPARE Analysis
inferred← citeshttps://doi.org/10.4238/2015.december.21.18openalex-snapshot
O-naphthoquinone isolated from Capraria biflora L. induces selective cytotoxicity in tumor cell lines
inferred← citeshttps://doi.org/10.70675/587bc6baz7fbdz49dbza041z2409fe571854openalex-snapshot
Physico-chemical approach to the formulation of beta-lapachone, and its complexes with cyclodextrins, in liposomes
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