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Anticancer Activity of Stilbene‐Based Derivatives
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Comparison of the effects of the chemopreventive agent resveratrol and its synthetic analog trans 3,4,5,4′‐tetramethoxystilbene (DMU‐212) on adenoma development in the ApcMin+ mouse and cyclooxygenase‐2 in human‐derived colon cancer cells
inferredcites →https://doi.org/10.1002/ijc.24336openalex-snapshot
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inferredcites →https://doi.org/10.1002/mc.20352openalex-snapshot
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inferredcites →https://doi.org/10.1002/mnfr.200400094openalex-snapshot
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inferredcites →https://doi.org/10.1002/mnfr.200600135openalex-snapshot
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inferredcites →https://doi.org/10.1002/mnfr.200700202openalex-snapshot
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inferredcites →https://doi.org/10.1002/mnfr.200900320openalex-snapshot
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inferredcites →https://doi.org/10.1002/mnfr.201100122openalex-snapshot
Resveratrol derivatives as promising chemopreventive agents with improved potency and selectivity
inferredcites →https://doi.org/10.1007/s00280-008-0704-zopenalex-snapshot
Resveratrol analog trans 3,4,5,4′-tetramethoxystilbene (DMU-212) mediates anti-tumor effects via mechanism different from that of resveratrol
inferredcites →https://doi.org/10.1007/s00280-010-1525-4openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bcp.2006.12.028openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2009.05.007openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2010.03.019openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2010.05.042openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2012.07.012openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmc.2013.03.072openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2003.10.038openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2006.03.028openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2011.08.090openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2012.04.062openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2012.09.111openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2014.10.009openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.bmcl.2015.05.019openalex-snapshot
Heteroaromatic analogs of the resveratrol analog DMU-212 as potent anti-cancer agents
inferredcites →https://doi.org/10.1016/j.bmcl.2016.01.069openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.cell.2006.10.018openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.drudis.2010.07.005openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2005.10.012openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2010.03.024openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2010.05.019openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2011.03.049openalex-snapshot
Anticancer effects of the metabolic products of the resveratrol analogue, DMU-212: Structural requirements for potency
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Discovery of gemfibrozil analogues that activate PPARα and enhance the expression of gene CPT1A involved in fatty acids catabolism
inferredcites →https://doi.org/10.1016/j.ejmech.2012.06.015openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2012.11.021openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2012.12.008openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2014.10.083openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2015.03.030openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2015.03.057openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2015.04.038openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.ejmech.2015.09.014openalex-snapshot
Inhibitory effect of cytotoxic stilbenes related to resveratrol on the expression of the VEGF, hTERT and c-Myc genes
inferredcites →https://doi.org/10.1016/j.ejmech.2015.11.014openalex-snapshot
Orally available stilbene derivatives as potent HDAC inhibitors with antiproliferative activities and antitumor effects in human tumor xenografts
inferredcites →https://doi.org/10.1016/j.ejmech.2016.05.012openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.foodchem.2014.08.130openalex-snapshot
Photo-induced chemical reaction of trans-resveratrol
inferredcites →https://doi.org/10.1016/j.jconrel.2011.09.083openalex-snapshot
Administration of resveratrol: What formulation solutions to bioavailability limitations?
inferredcites →https://doi.org/10.1016/j.jpba.2008.10.042openalex-snapshot
A rapid HPLC method for the quantification of 3,5,4′-trimethoxy-trans-stilbene (TMS) in rat plasma and its application in pharmacokinetic study
inferredcites →https://doi.org/10.1016/j.jpba.2011.08.020openalex-snapshot
Determination of trans-2,4,3′,4′,5′-pentamethoxystilbene in rat plasma and its application to a pharmacokinetic study
inferredcites →https://doi.org/10.1016/j.jss.2011.09.054openalex-snapshot
Pterostilbene and Cancer: Current Review
inferredcites →https://doi.org/10.1016/j.lfs.2016.07.021openalex-snapshot
Polyphenols in dementia: From molecular basis to clinical trials
inferredcites →https://doi.org/10.1016/j.nut.2015.08.017openalex-snapshot
Beneficial action of resveratrol: How and why?
inferredcites →https://doi.org/10.1016/j.pharep.2014.03.012openalex-snapshot
The effect of resveratrol and its methylthio-derivatives on NF-κB and AP-1 signaling pathways in HaCaT keratinocytes
inferredcites →https://doi.org/10.1016/j.phytochem.2012.01.012openalex-snapshot
Prenylated cinnamate and stilbenes from Kangaroo Island propolis and their antioxidant activity
inferredcites →https://doi.org/10.1016/j.semcancer.2015.11.001openalex-snapshot
Resveratrol for breast cancer prevention and therapy: Preclinical evidence and molecular mechanisms
inferredcites →https://doi.org/10.1016/j.taap.2015.05.020openalex-snapshot
Structural modification of resveratrol leads to increased anti-tumor activity, but causes profound changes in the mode of action
inferredcites →https://doi.org/10.1016/j.vascn.2016.11.001openalex-snapshot
Drug-selected cell line panels for evaluation of the pharmacokinetic consequences of multidrug resistance proteins
inferredcites →https://doi.org/10.1016/s0006-2952(02)01618-0openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0031-9422(00)80766-9openalex-snapshot
Non-alkaloidal constituents of Virola elongata bark
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Antitumor Agents. Part 204: Synthesis and Biological Evaluation of Substituted 2-Aryl Quinazolinones
inferredcites →https://doi.org/10.1016/s1875-5364(15)30029-7openalex-snapshot
Synthesis and cytotoxic activities of E-resveratrol derivatives
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Quantum Chemistry Calculation-Aided Structural Optimization of Combretastatin A-4-like Tubulin Polymerization Inhibitors: Improved Stability and Biological Activity
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00619openalex-snapshot
Resveratrol-Related Polymethoxystilbene Glycosides: Synthesis, Antiproliferative Activity, and Glycosidase Inhibition
inferredcites →https://doi.org/10.1021/cb200435yopenalex-snapshot
Methoxy Stilbenes as Potent, Specific, Untransported, and Noncytotoxic Inhibitors of Breast Cancer Resistance Protein
inferredcites →https://doi.org/10.1021/ct400647wopenalex-snapshot
Photoisomerization of Stilbene: The Detailed XMCQDPT2 Treatment
inferredcites →https://doi.org/10.1021/jf000745oopenalex-snapshot
Method for the Quantitative Extraction of Resveratrol and Piceid Isomers in Grape Berry Skins. Effect of Powdery Mildew on the Stilbene Content
inferredcites →https://doi.org/10.1021/jf104901gopenalex-snapshot
Resveratrol Metabolites Do Not Elicit Early Pro-apoptotic Mechanisms in Neuroblastoma Cells
inferredcites →https://doi.org/10.1021/jm00090a021openalex-snapshot
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inferredcites →https://doi.org/10.1021/jm030785uopenalex-snapshot
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inferredcites →https://doi.org/10.1021/jm0512903openalex-snapshot
Medicinal Chemistry of Combretastatin A4: Present and Future Directions
inferredcites →https://doi.org/10.1021/jm1002414openalex-snapshot
Identification of CKD-516: A Potent Tubulin Polymerization Inhibitor with Marked Antitumor Activity against Murine and Human Solid Tumors
inferredcites →https://doi.org/10.1021/jm100274copenalex-snapshot
Selective Synthesis and Biological Evaluation of Sulfate-Conjugated Resveratrol Metabolites
inferredcites →https://doi.org/10.1021/jm101248vopenalex-snapshot
Fluorinated N,N-Dialkylaminostilbenes for Wnt Pathway Inhibition and Colon Cancer Repression
inferredcites →https://doi.org/10.1021/jm200639ropenalex-snapshot
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inferredcites →https://doi.org/10.1021/jm5004864openalex-snapshot
2′,6′-Dihalostyrylanilines, Pyridines, and Pyrimidines for the Inhibition of the Catalytic Subunit of Methionine S-Adenosyltransferase-2
inferredcites →https://doi.org/10.1021/np400188mopenalex-snapshot
Effect of Resveratrol-Related Stilbenoids on Biomembrane Models
inferredcites →https://doi.org/10.1038/aps.2013.60openalex-snapshot
Trans-3,4,5,4′-tetramethoxystilbene, a resveratrol analog, potently inhibits angiogenesis in vitro and in vivo
inferredcites →https://doi.org/10.1038/nature11127openalex-snapshot
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inferredcites →https://doi.org/10.1038/nrc2347openalex-snapshot
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inferredcites →https://doi.org/10.1038/sj.bjc.6601568openalex-snapshot
Pharmacokinetics in mice and growth-inhibitory properties of the putative cancer chemopreventive agent resveratrol and the synthetic analogue trans 3,4,5,4′-tetramethoxystilbene
inferredcites →https://doi.org/10.1039/c0np00055hopenalex-snapshot
Natural glycoconjugates with antitumor activity
inferredcites →https://doi.org/10.1039/c2np20049jopenalex-snapshot
Natural stilbenoids: distribution in the plant kingdom and chemotaxonomic interest in Vitaceae
inferredcites →https://doi.org/10.1039/c3md00130jopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c3md00317eopenalex-snapshot
3,4,2′-Trimethoxy-trans-stilbene – a potent CYP1B1 inhibitor
inferredcites →https://doi.org/10.1039/c4md00115jopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c4md00478gopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c5md00139kopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c5md00151jopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c5md00197hopenalex-snapshot
Inhibitory effect of cytotoxic nitrogen-containing heterocyclic stilbene analogues on VEGF protein secretion and VEGF, hTERT and c-Myc gene expression
inferredcites →https://doi.org/10.1042/bj20071373openalex-snapshot
Kinetic, thermodynamic and X-ray structural insights into the interaction of melatonin and analogues with quinone reductase 2
inferredcites →https://doi.org/10.1042/bst0351156openalex-snapshot
Resveratrol as an antioxidant and pro-oxidant agent: mechanisms and clinical implications
inferredcites →https://doi.org/10.1055/s-0029-1185533openalex-snapshot
Antitumor Activity of Resveratrol and its Sulfated Metabolites against Human Breast Cancer Cells
inferredcites →https://doi.org/10.1074/jbc.m101846200openalex-snapshot
Specific Structural Determinants Are Responsible for the Antioxidant Activity and the Cell Cycle Effects of Resveratrol
inferredcites →https://doi.org/10.1074/jbc.m206452200openalex-snapshot
A Novel Antioxidant Mechanism of Ebselen Involving Ebselen Diselenide, a Substrate of Mammalian Thioredoxin and Thioredoxin Reductase
inferredcites →https://doi.org/10.1089/ars.2008.2412openalex-snapshot
Resveratrol: Its Biologic Targets and Functional Activity
inferredcites →https://doi.org/10.1111/cbdd.12425openalex-snapshot
In vitro Antiviral Effects and 3 D QSAR Study of Resveratrol Derivatives as Potent Inhibitors of Influenza H 1 N 1 Neuraminidase
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DNA polymerase lambda directly binds to proliferating cell nuclear antigen through its confined C‐terminal region
inferredcites →https://doi.org/10.1111/j.1440-1746.2006.04757.xopenalex-snapshot
Elevated plasma resistin concentrations in patients with liver cirrhosis
inferredcites →https://doi.org/10.1111/j.1440-1746.2007.05289.xopenalex-snapshot
S‐Adenosylmethionine in cell growth, apoptosis and liver cancer
inferredcites →https://doi.org/10.1111/j.1474-9726.2006.00259.xopenalex-snapshot
Design and synthesis of compounds that extend yeast replicative lifespan
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Anti‐inflammatory effects of resveratrol: possible role in prevention of age‐related cardiovascular disease
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Resveratrol nanoformulation for cancer prevention and therapy
inferredcites →https://doi.org/10.1155/2013/575482openalex-snapshot
A Review of Pterostilbene Antioxidant Activity and Disease Modification
inferredcites →https://doi.org/10.1155/2015/340520openalex-snapshot
Polyphenol Stilbenes: Molecular Mechanisms of Defence against Oxidative Stress and Aging-Related Diseases
inferredcites →https://doi.org/10.1158/0008-5472.can-07-0056openalex-snapshot
Effects of Tetramethoxystilbene on Hormone-Resistant Breast Cancer Cells: Biological and Biochemical Mechanisms of Action
inferredcites →https://doi.org/10.1172/jci58128openalex-snapshot
Epoxyeicosanoids stimulate multiorgan metastasis and tumor dormancy escape in mice
inferredcites →https://doi.org/10.1177/1934578x1200700822openalex-snapshot
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inferredcites →https://doi.org/10.1186/1471-2210-8-15openalex-snapshot
Methoxylation enhances stilbene bioactivity in Caenorhabditis elegans
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Potential Cancer-Chemopreventive Activities of Wine Stilbenoids and Flavans Extracted From Grape (Vitis vinifera) Cell Cultures
inferredcites →https://doi.org/10.1358/dof.2002.027.05.668645openalex-snapshot
Combretastatin anticancer drugs
inferredcites →https://doi.org/10.1517/13543776.2013.834888openalex-snapshot
Resveratrol derivatives: a patent review (2009 – 2012)
inferredcites →https://doi.org/10.1517/17425247.2011.581655openalex-snapshot
New delivery systems to improve the bioavailability of resveratrol
inferredcites →https://doi.org/10.1530/erc-13-0171openalex-snapshot
Resveratrol and cancer: focus on in vivo evidence
inferredcites →https://doi.org/10.2174/092986712799945085openalex-snapshot
Resveratrol in Medicinal Chemistry: A Critical Review of its Pharmacokinetics, Drug-Delivery, and Membrane Interactions
inferredcites →https://doi.org/10.2174/0929867323666160517121629openalex-snapshot
The Use of Stilbene Scaffold in Medicinal Chemistry and Multi- Target Drug Design
inferredcites →https://doi.org/10.2174/138161209787315594openalex-snapshot
Designing Multiple Ligands – Medicinal Chemistry Strategies and Challenges
inferredcites →https://doi.org/10.2174/1381612811319100013openalex-snapshot
Design of Combretastatin A-4 Analogs as Tubulin Targeted Vascular Disrupting Agent with Special Emphasis on Their Cis-Restricted Isomers
inferredcites →https://doi.org/10.2174/138955707782795647openalex-snapshot
Combretastatin A-4 Analogs as Anticancer Agents
inferredcites →https://doi.org/10.2174/157340641001131226123613openalex-snapshot
Effect of Stilbene and Chalcone Scaffolds Incorporation in Clofibric Acid on PPARα . Agonistic Activity
inferredcites →https://doi.org/10.2174/1573406412666160502153700openalex-snapshot
New Hopes in Cancer Battle - A Review of New Molecules and Treatment Strategies
inferredcites →https://doi.org/10.2174/187152011795677427openalex-snapshot
Resveratrol and Its Analogues: Promising Antitumor Agents
inferredcites →https://doi.org/10.21873/anticanres.11146openalex-snapshot
Discovery of Anticancer Agents of Diverse Natural Origin
inferredcites →https://doi.org/10.2478/s11658-013-0094-zopenalex-snapshot
Tubulin-interactive stilbene derivatives as anticancer agents
inferredcites →https://doi.org/10.3390/nu8080515openalex-snapshot
Natural Polyphenols for Prevention and Treatment of Cancer
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113128zenodo-depositor-declared
Stilbenes: Source plants, chemistry, biosynthesis, pharmacology, application and problems related to their clinical Application-A comprehensive review
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inferred← citeshttps://doi.org/10.1002/cmdc.201900128openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ddr.21525openalex-snapshot
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Regioselective Hydroxylation of Stilbenes by White‐Rot Fungal P450s Enables Preparative‐Scale Synthesis of Stilbenoids
inferred← citeshttps://doi.org/10.1002/ejoc.202300552openalex-snapshot
Multicomponent and Metal‐Free Diels–Alder/Aromatization Approach to the Stereospecific Synthesis of E‐(Hetero)Stilbenes and Diarylacetylenes
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Stereoselective Synthesis of ( E )‐1,2‐Diarylethene via Palladium‐Catalyzed Decarboxylative Cross‐Coupling of Phenylacrylic Acids with Aryl Halides: Access to Resveratrol, Pinosylvin, and Pterostilbene
inferred← citeshttps://doi.org/10.1002/fsn3.3046openalex-snapshot
Stilbene‐based derivatives as potential inhibitors of trimethylamine ( TMA )‐lyase affect gut microbiota in coronary heart disease
inferred← citeshttps://doi.org/10.1002/fsn3.71259openalex-snapshot
Antioxidant Potential of Polyphenolic Compounds, Sources, Extraction, Purification and Characterization Techniques: A Focused Review
inferred← citeshttps://doi.org/10.1002/jat.4452openalex-snapshot
Novel ferrocene‐containing triacyl derivative of resveratrol improves viability parameters in ovary cells
inferred← citeshttps://doi.org/10.1002/jccs.202000501openalex-snapshot
Novel phenolic compounds by DFT : Electronic effects on antioxidant activity of 4‐vinylphenol derivatives
inferred← citeshttps://doi.org/10.1002/jsfa.10152openalex-snapshot
Resveratrol: a review of plant sources, synthesis, stability, modification and food application
inferred← citeshttps://doi.org/10.1002/mnfr.202300479openalex-snapshot
Molecular Efficacy of Gnetin C as Dual‐Targeted Therapy for Castrate‐Resistant Prostate Cancer
inferred← citeshttps://doi.org/10.1002/mnfr.202400414openalex-snapshot
The Inhibitory Effects of the Natural Stilbene Piceatannol on Lactate Transport In Vitro Mediated by Monocarboxylate Transporters
inferred← citeshttps://doi.org/10.1002/slct.202303375openalex-snapshot
Synthesis of Hydroxylated Stilbenes in a Batch and Flow Reactor: An Overview
inferred← citeshttps://doi.org/10.1002/slct.202402433openalex-snapshot
Synthesis of para ‐Carboxamidostilbene Derivatives as Antihyperglycemia Agents and Their In Silico ADMET and Molecular Docking Studies
inferred← citeshttps://doi.org/10.1007/978-3-031-04998-9_12openalex-snapshot
Polypharmacology in Drug Design and Discovery—Basis for Rational Design of Multitarget Drugs
inferred← citeshttps://doi.org/10.1007/978-981-13-7154-7_3openalex-snapshot
Microbial Hosts as a Promising Platform for Polyphenol Production
inferred← citeshttps://doi.org/10.1007/978-981-95-0343-8_17openalex-snapshot
Biotic and Abiotic Elicitation for Enhanced Production of Stilbenes
inferred← citeshttps://doi.org/10.1007/s00044-019-02351-3openalex-snapshot
Synthesis and cytotoxic effects on pancreatic cancer cells of resveratrol analogs
inferred← citeshttps://doi.org/10.1007/s00044-023-03018-wopenalex-snapshot
Synthesis, cytotoxicity, Pan-HDAC inhibitory activity and docking study of new N-(2-aminophenyl)-2-methylquinoline-4-carboxamide and (E)-N-(2-aminophenyl)-2-styrylquinoline-4-carboxamide derivatives as anticancer agents
inferred← citeshttps://doi.org/10.1007/s00894-021-04719-yopenalex-snapshot
Condensed-phase relative Gibbs free energy and E/Z descriptors for 2-acetylthiophene and 2-acetylthiophene-N1-phenyl thiosemicarbazones
inferred← citeshttps://doi.org/10.1007/s00894-024-06192-9openalex-snapshot
A DFT analysis of the antioxidant capacity of scopolin and scopoletin
inferred← citeshttps://doi.org/10.1007/s11030-021-10354-9openalex-snapshot
Molecular dynamics simulations, docking and MMGBSA studies of newly designed peptide-conjugated glucosyloxy stilbene derivatives with tumor cell receptors
inferred← citeshttps://doi.org/10.1007/s11240-025-03310-0openalex-snapshot
Antioxidant and antimicrobial capacities of complex organic extracts containing stilbenes derivatives obtained from Vitis vinifera Pinot Noir hairy roots cultures for potential application in cosmetics
inferred← citeshttps://doi.org/10.1007/s11696-026-05153-1openalex-snapshot
Classification and QSAR of the anticancer activity of (E)-stilbenes
inferred← citeshttps://doi.org/10.1007/s13205-026-04906-9openalex-snapshot
Bioactive plant metabolites with antihyperglycemic properties: prospects for the prevention and treatment of diabetes mellitus
inferred← citeshttps://doi.org/10.1007/s41981-025-00349-0openalex-snapshot
Application of natural deep eutectic solvents in the continuous process for synthesis of resveratrol analogues by the Wittig reaction
inferred← citeshttps://doi.org/10.1016/b978-0-443-13821-8.00002-0openalex-snapshot
Metabolization pathways and bioavailability of polyphenols
inferred← citeshttps://doi.org/10.1016/b978-0-443-30170-4.00011-5openalex-snapshot
Chemistry and pharmacology of lignans and stilbenes reported in African medicinal plants
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103719openalex-snapshot
Methoxy-enriched cationic stilbenes as anticancer therapeutics
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103997openalex-snapshot
Synthesis of furocoumarin–stilbene hybrids as potential multifunctional drugs against multiple biochemical targets associated with Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104017openalex-snapshot
Diaryl disulfides and thiosulfonates as combretastatin A-4 analogues: Synthesis, cytotoxicity and antitubulin activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107930openalex-snapshot
Combretastatin A-4 based compounds as potential anticancer agents: A review
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.07.048openalex-snapshot
Synthesis and biological evaluation of cis-restrained carbocyclic combretastatin A-4 analogs: Influence of the ring size and saturation on cytotoxic properties
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.11.009openalex-snapshot
(E)-3-(3,4,5-Trimethoxyphenyl)-1-(pyridin-4-yl)prop-2-en-1-one, a heterocyclic chalcone is a potent and selective CYP1A1 inhibitor and cancer chemopreventive agent
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.04.004openalex-snapshot
Stereocontrolled synthesis of (E)-stilbene derivatives by palladium-catalyzed Suzuki-Miyaura cross-coupling reaction
inferred← citeshttps://doi.org/10.1016/j.cherd.2025.06.012openalex-snapshot
Push button, automated flow synthesis of biaryls and stilbenes using palladium-catalysed cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.cis.2025.103424openalex-snapshot
Interactions between β-lactoglobulin and polyphenols: Mechanisms, properties, characterization, and applications
inferred← citeshttps://doi.org/10.1016/j.crtox.2023.100113openalex-snapshot
The cancer preventive activity and mechanisms of prenylated resveratrol and derivatives
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.111000openalex-snapshot
Photochromic heteroarylethenes with fast thermal isomerization kinetics
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113655openalex-snapshot
Silyl resveratrol derivatives as potential therapeutic agents for neurodegenerative and neurological diseases
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113737openalex-snapshot
Synthesis, structure-activity relationships and molecular docking studies of phenyldiazenyl sulfonamides as aromatase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114242openalex-snapshot
Resveratrol-based compounds and neurodegeneration: Recent insight in multitarget therapy
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114962openalex-snapshot
Resveratrol derivatives: Synthesis and their biological activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.117021openalex-snapshot
A novel life for antitumor combretastatins: Recent developments of hybrids, prodrugs, combination therapies, and antibody-drug conjugates
inferred← citeshttps://doi.org/10.1016/j.ejmech.2026.118967openalex-snapshot
Beyond conventional 5-Fluorouracil: Recent medicinal chemistry strategies to enhance its anticancer efficacy
inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174660openalex-snapshot
The natural (poly)phenols as modulators of microglia polarization via TLR4/NF-κB pathway exert anti-inflammatory activity in ischemic stroke
inferred← citeshttps://doi.org/10.1016/j.ejphar.2022.174847openalex-snapshot
Promising heterocycle-based scaffolds in recent (2019–2021) anti-Alzheimer's drug design and discovery
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2025.114142openalex-snapshot
Synthesis of a dual-function monomer and its corresponding polymer for the valorisation of stilbenes from grape canes
inferred← citeshttps://doi.org/10.1016/j.fbio.2021.101297openalex-snapshot
Potential applications and preliminary mechanism of action of dietary polyphenols against hyperuricemia: A review
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105331openalex-snapshot
Six undescribed derivatives of stilbene isolated from Lindera reflexa Hemsl. and their anti-tumor and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.107034openalex-snapshot
Pharmacological insights on multifaceted therapeutic applications of stilbenoids: A comprehensive updates
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e25990openalex-snapshot
Metabolomic analysis revealed the edible and extended-application potential of specific Polygonum multiflorum tissues
inferred← citeshttps://doi.org/10.1016/j.hpj.2024.12.004openalex-snapshot
VqBGH52 enhances the accumulation of trans-resveratrol through hydrolysis of trans-piceid and resistance to powdery mildew in Chinese wild grapevine
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.143203openalex-snapshot
Composition and distribution of phenolic compounds of optimized bilberry microcapsules using wood hemicelluloses as protecting materials
inferred← citeshttps://doi.org/10.1016/j.jece.2026.121773openalex-snapshot
Selective fixed-bed fractionation of stilbene subfamilies from grape cane waste using a pyridine-amide adsorbent
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2020.112927openalex-snapshot
UV-responsive glycosomes as frameworks for FRET: The quest for bio-inspired energy transfer systems
inferred← citeshttps://doi.org/10.1016/j.neuint.2019.03.021openalex-snapshot
PPAR-γ agonist GL516 reduces oxidative stress and apoptosis occurrence in a rat astrocyte cell line
inferred← citeshttps://doi.org/10.1016/j.phrs.2021.105959openalex-snapshot
Evidence of a dual mechanism of action underlying the anti-proliferative and cytotoxic effects of ammonium-alkyloxy-stilbene-based α7- and α9-nicotinic ligands on glioblastoma cells
inferred← citeshttps://doi.org/10.1016/j.phymed.2018.04.010openalex-snapshot
trans-3-Methoxy-5-hydroxystilbene (MHS) from the rhizome of Alpinia nantonensis inhibits metastasis in human lung cancer cells
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113241openalex-snapshot
Identification and structural elucidation of bioactive compounds from Scirpoides holoschoenus
inferred← citeshttps://doi.org/10.1016/j.prenap.2025.100173openalex-snapshot
Stilbenes in breast cancer treatment: Nanostilbenes an approach to improve therapeutic efficacy
inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103577openalex-snapshot
In silico investigation of natural stilbenes from berries and grapes and their derivatives as potential ASPH inhibitors for hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.seppur.2024.127798openalex-snapshot
Purification of stilbenes from grape stems in a continuous process based on photo-molecularly imprinted adsorbents and hydroalcoholic solvents
inferred← citeshttps://doi.org/10.1016/j.synbio.2025.07.010openalex-snapshot
Integrated protein and metabolic engineering enable high-yield biosynthesis of resveratrol derivatives in Yarrowia lipolytica
inferred← citeshttps://doi.org/10.1016/s1875-5364(22)60141-9openalex-snapshot
Promising natural lysine specific demethylase 1 inhibitors for cancer treatment: advances and outlooks
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c03020openalex-snapshot
Utilization of Nanotechnology to Improve the Application and Bioavailability of Phytochemicals Derived from Waste Streams
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c00326openalex-snapshot
Trends in the Potential of Stilbenes to Improve Plant Stress Tolerance: Insights of Plant Defense Mechanisms in Response to Biotic and Abiotic Stressors
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c02030openalex-snapshot
Design, Synthesis, and Antibacterial Activity of Stilbene Derivatives against Phytopathogenic Bacteria
inferred← citeshttps://doi.org/10.1021/acs.langmuir.4c04717openalex-snapshot
Spectroscopic Manifestation of a Weak van der Waals Interaction Between trans-Stilbene and Hexagonal Boron Nitride Surface
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00538openalex-snapshot
Regioselective Synthesis of α-Functional Stilbenes via Precise Control of Rapid cis–trans Isomerization in Flow
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01754openalex-snapshot
One-Pot Intermolecular Reductive Cross-Coupling of Deactivated Aldehydes to Unsymmetrically 1,2-Disubstituted Alkenes
inferred← citeshttps://doi.org/10.1021/acschemneuro.9b00574openalex-snapshot
Native Mass Spectrometry Based Method for Studying the Interactions between Superoxide Dismutase 1 and Stilbenoids
inferred← citeshttps://doi.org/10.1038/s41598-018-30860-5openalex-snapshot
Density functional theory study of the role of benzylic hydrogen atoms in the antioxidant properties of lignans
inferred← citeshttps://doi.org/10.1038/s41598-025-01051-wopenalex-snapshot
Synthesis and evaluation of quinolinvinyl-phenoxy-1,2,3-triazole-acetamide hybrids against breast cancer
inferred← citeshttps://doi.org/10.1039/c8gc00931gopenalex-snapshot
Alcohol-based Michaelis–Arbuzov reaction: an efficient and environmentally-benign method for C–P(O) bond formation
inferred← citeshttps://doi.org/10.1039/c9md00286copenalex-snapshot
Druggability profile of stilbene-derived PPAR agonists: determination of physicochemical properties and PAMPA study
inferred← citeshttps://doi.org/10.1039/c9nj06178aopenalex-snapshot
Copper-catalyzed alkenylation of novel N -iodoarylated allylic ketopiperazinonates with unactivated alkenes
inferred← citeshttps://doi.org/10.1039/d0ob01139hopenalex-snapshot
E , Z -Selectivity in the reductive cross-coupling of two benzaldehydes to stilbenes under substrate control
inferred← citeshttps://doi.org/10.1039/d2ob01982eopenalex-snapshot
Recent advances in synthesis of stilbene derivatives via cross-coupling reaction
inferred← citeshttps://doi.org/10.1039/d2ra03684copenalex-snapshot
Synthesis, antitumor activity, 3D-QSAR and molecular docking studies of new iodinated 4-(3 H )-quinazolinones 3 N -substituted
inferred← citeshttps://doi.org/10.1039/d4ra02867hopenalex-snapshot
Medicinal chemistry perspective on the structure–activity relationship of stilbene derivatives
inferred← citeshttps://doi.org/10.1039/d5np00091bopenalex-snapshot
Charting the path for l -tyrosine derivatives: from engineering strategies to microbial cell factories
inferred← citeshttps://doi.org/10.1080/10426507.2018.1543305openalex-snapshot
Reactivity patterns of benzhydryl(mesityl)phosphane oxide – a potential intermediate in carbonyl-carbonyl coupling reactions?
inferred← citeshttps://doi.org/10.1093/mtomcs/mfae002openalex-snapshot
Cyclometalated ruthenium complexes overcome cisplatin resistance through PI3K/mTOR/Nrf2 signaling pathway
inferred← citeshttps://doi.org/10.1109/atigb63471.2024.10717759openalex-snapshot
An In Silico Evaluation Of The Multifunctional Activity Of Crocetin Against Neurodegenerative Disease
inferred← citeshttps://doi.org/10.1111/cbdd.13958openalex-snapshot
Synthesis and activities of acetylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.1139/cjc-2022-0164openalex-snapshot
Structural, DFT calculations and photophysical and photochemical characteristics of 1-((E)-2-phenylethenyl)-2-(4-(2-((E)-2-phenylethenyl) phenoxy) butoxy) benzene (PPPBB)
inferred← citeshttps://doi.org/10.1186/s12934-024-02541-8openalex-snapshot
Identification of a polyphenol O-methyltransferase with broad substrate flexibility in Streptomyces albidoflavus J1074
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1351595/v1openalex-snapshot
Super – Fluorescence Quenching of 1-(E)-styryl-2-(4-(2-(E) - styrylphenoxy) Butoxy)Benzene (Alkoxy Bridged Styryl Benzene)(PPPBB) Colloidal Silver and Gold Nanoparticles
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1355256/v1openalex-snapshot
Structural, DFT calculations, photophysical and photochemical characteristics of 1-((E)-2-phenylethenyl)-2-(4-(2-((E)-2-phenylethenyl) phenoxy) butoxy) benzene (PPPBB)
inferred← citeshttps://doi.org/10.2174/0109298673263854231009063053openalex-snapshot
Synthesis and Selective Anticancer Activity Evaluation of 2-phenylacrylonitrile Derivatives as Tubulin Inhibitors
inferred← citeshttps://doi.org/10.2174/0109298673296147240405113328openalex-snapshot
Research Progress and Prospect of Nitrogen-containing Heterocycle in Anti-gastric Cancer Drugs: A Review
inferred← citeshttps://doi.org/10.2174/0118756298307930240531072440openalex-snapshot
A Comprehensive Review on History, Sources, Biosynthesis, Chemical Synthesis and Applications of Stilbenes
inferred← citeshttps://doi.org/10.2174/0929867326666190121143252openalex-snapshot
Metabolism of Rhaponticin and Activities of its Metabolite, Rhapontigenin: A Review
inferred← citeshttps://doi.org/10.2174/1385272827666230911115740openalex-snapshot
Synthesis, Cytotoxic Potential, and Molecular Docking Studies of Ortho-carboxamidostilbene Analogs
inferred← citeshttps://doi.org/10.2174/1389557519666190603085026openalex-snapshot
PPAR Ligands Containing Stilbene Scaffold
inferred← citeshttps://doi.org/10.2174/1567201819666220823155526openalex-snapshot
Nanoformulations of Plant-Derived Compounds as Emerging Therapeutic Approach for Colorectal Cancer
inferred← citeshttps://doi.org/10.2174/1871520618666180903100835openalex-snapshot
Design, Synthesis, In vitro Cytotoxic Activity Evaluation, and Study of Apoptosis Inducing Effect of New Styrylimidazo[1,2-a]Pyridines as Potent Anti-Breast Cancer Agents
inferred← citeshttps://doi.org/10.2174/1874104501913010007openalex-snapshot
Inhibition of PPARγ by Natural Compounds as a Promising Strategy in Obesity and Diabetes
inferred← citeshttps://doi.org/10.2174/221031551205220615151759openalex-snapshot
Meet the Editorial Board Member
inferred← citeshttps://doi.org/10.2174/9789815079098122010005openalex-snapshot
Recent Development of Hybrids and Derivatives of Resveratrol in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.21873/anticanres.12038openalex-snapshot
Search for New Type of Anticancer Drugs with High Tumor Specificity and Less Keratinocyte Toxicity
inferred← citeshttps://doi.org/10.2217/nnm-2022-0133openalex-snapshot
Molecular Insights and Therapeutic Implications of Nanoengineered Dietary Polyphenols for Targeting Lung Carcinoma: Part I
inferred← citeshttps://doi.org/10.26434/chemrxiv-2021-kkftp-v2openalex-snapshot
Synthesis of Stilbenes Using Various Catalysts and Investigation of their Optical Properties
inferred← citeshttps://doi.org/10.3126/njb.v7i1.26955openalex-snapshot
Polyphenols: Nature's Gift as dietary phytoconstituents against different human ailments
inferred← citeshttps://doi.org/10.3389/fchem.2022.872366openalex-snapshot
Pyrene Functionalized Highly Reduced Graphene Oxide-palladium Nanocomposite: A Novel Catalyst for the Mizoroki-Heck Reaction in Water
inferred← citeshttps://doi.org/10.3389/fchem.2023.1158717openalex-snapshot
On-line identification of the chemical constituents of Polygoni Multiflori Radix by UHPLC-Q-ToF MS/MS
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1148513openalex-snapshot
Microbial biotransformation to obtain stilbene methylglucoside with GPR119 agonistic activity
inferred← citeshttps://doi.org/10.3389/fphar.2024.1442297openalex-snapshot
The application of rhubarb concoctions in traditional Chinese medicine and its compounds, processing methods, pharmacology, toxicology and clinical research
inferred← citeshttps://doi.org/10.3390/antibiotics10091034openalex-snapshot
Heteroaryl-Ethylenes as New Lead Compounds in the Fight against High Priority Bacterial Strains
inferred← citeshttps://doi.org/10.3390/antibiotics9120891openalex-snapshot
Searching for New Tools to Counteract the Helicobacter pylori Resistance: The Positive Action of Resveratrol Derivatives
inferred← citeshttps://doi.org/10.3390/antiox10040534openalex-snapshot
Targeting AKT/mTOR and Bcl-2 for Autophagic and Apoptosis Cell Death in Lung Cancer: Novel Activity of a Polyphenol Compound
inferred← citeshttps://doi.org/10.3390/antiox11050859openalex-snapshot
Redox Profiling of Selected Apulian Red Wines in a Single Minute
inferred← citeshttps://doi.org/10.3390/antiox13111425openalex-snapshot
The Potential of Plant Extracts Used in Cosmetic Product Applications—Antioxidants Delivery and Mechanism of Actions
inferred← citeshttps://doi.org/10.3390/antiox8100467openalex-snapshot
In Vitro Toxicity Assessment of Stilbene Extract for Its Potential Use as Antioxidant in the Wine Industry
inferred← citeshttps://doi.org/10.3390/biom10081111openalex-snapshot
More Than Resveratrol: New Insights into Stilbene-Based Compounds
inferred← citeshttps://doi.org/10.3390/biom9070268openalex-snapshot
Carbon-Carbon Double Bond and Resorcinol in Resveratrol and Its Analogues: What Is the Characteristic Structure in Quenching Singlet Oxygen?
inferred← citeshttps://doi.org/10.3390/cimb47030204openalex-snapshot
Pinosylvin: A Multifunctional Stilbenoid with Antimicrobial, Antioxidant, and Anti-Inflammatory Potential
inferred← citeshttps://doi.org/10.3390/f15101782openalex-snapshot
Multidimensional Exploration of Wood Extractives: A Review of Compositional Analysis, Decay Resistance, Light Stability, and Staining Applications
inferred← citeshttps://doi.org/10.3390/ijms19092651openalex-snapshot
Structure-Based Classification and Anti-Cancer Effects of Plant Metabolites
inferred← citeshttps://doi.org/10.3390/ijms20112716openalex-snapshot
Stilbene Compounds Inhibit Tumor Growth by the Induction of Cellular Senescence and the Inhibition of Telomerase Activity
inferred← citeshttps://doi.org/10.3390/ijms24031977openalex-snapshot
Resveratrol Derivative Exhibits Marked Antiproliferative Actions, Affecting Stemness in Pancreatic Cancer Cells
inferred← citeshttps://doi.org/10.3390/ijms27020719openalex-snapshot
Anticancer Activity of 2,3′-Dihydroxy-5′-Methoxystilbene Against NSCLC Cell Lines Through AKT-Dependent Mechanisms: A Comprehensive In Vitro and Computational Analysis
inferred← citeshttps://doi.org/10.3390/ijms27104512openalex-snapshot
Structural Optimization of Pterostilbene, a Promising Lead Molecule, and Evaluation of Its Derivatives via ADMET Prediction and In Vitro/In Vivo Anti-Cerebral Ischemic Activity
inferred← citeshttps://doi.org/10.3390/metabo14070350openalex-snapshot
The Application of Resveratrol Derivatives in Oral Cells Reduces the Oxidative Stress Induced by Glucocorticoids
inferred← citeshttps://doi.org/10.3390/molecules23061271openalex-snapshot
Enzymatic Synthesis of a Novel Pterostilbene α-Glucoside by the Combination of Cyclodextrin Glucanotransferase and Amyloglucosidase
inferred← citeshttps://doi.org/10.3390/molecules24101896openalex-snapshot
Imaging Flow Cytometric Analysis of Stilbene-Dependent Apoptosis in Drug Resistant Human Leukemic Cell Lines
inferred← citeshttps://doi.org/10.3390/molecules24173145openalex-snapshot
The Impact of Temperature and Ethanol Concentration on the Global Recovery of Specific Polyphenols in an Integrated HPLE/RP Process on Carménère Pomace Extracts
inferred← citeshttps://doi.org/10.3390/molecules25122885openalex-snapshot
Determining the Effect of Pterostilbene on Insulin Secretion Using Chemoproteomics
inferred← citeshttps://doi.org/10.3390/molecules25235770openalex-snapshot
Synthesis and Biological Evaluation of Halogenated E-Stilbenols as Promising Antiaging Agents
inferred← citeshttps://doi.org/10.3390/molecules27041215openalex-snapshot
Computational Simulations Highlight the IL2Rα Binding Potential of Polyphenol Stilbenes from Fenugreek
inferred← citeshttps://doi.org/10.3390/molecules27061851openalex-snapshot
Phytochemical Constituents and Pharmacological Potential of Tamus communis Rhizomes
inferred← citeshttps://doi.org/10.3390/molecules27175373openalex-snapshot
Synthesis of Bio-Inspired 1,3-Diarylpropene Derivatives via Heck Cross-Coupling and Cytotoxic Evaluation on Breast Cancer Cells
inferred← citeshttps://doi.org/10.3390/molecules27227816openalex-snapshot
Resveratrol Analogues as Dual Inhibitors of Monoamine Oxidase B and Carbonic Anhydrase VII: A New Multi-Target Combination for Neurodegenerative Diseases?
inferred← citeshttps://doi.org/10.3390/molecules29174260openalex-snapshot
Radiolabeled Probes from Derivatives of Natural Compounds Used in Nuclear Medicine
inferred← citeshttps://doi.org/10.3390/molecules30091973openalex-snapshot
The Use of Plants That Seal Blood Vessels in Preparations Applied Topically to the Skin: A Review
inferred← citeshttps://doi.org/10.3390/molecules30091982openalex-snapshot
Stilbenes Against Alzheimer’s Disease: A Comprehensive Review of Preclinical Studies of Natural and Synthetic Compounds Combined with the Contributions of Developed Nanodrug Delivery Systems
inferred← citeshttps://doi.org/10.3390/molecules30244788openalex-snapshot
Bromo Analogues of Active 3,4,5,4′-Tetramethoxy-trans-stilbene (DMU-212)—A New Path of Research to Anticancer Agents
inferred← citeshttps://doi.org/10.3390/ph12020056openalex-snapshot
3-Vinylazetidin-2-Ones: Synthesis, Antiproliferative and Tubulin Destabilizing Activity in MCF-7 and MDA-MB-231 Breast Cancer Cells
inferred← citeshttps://doi.org/10.3390/ph14100984openalex-snapshot
Design, Synthesis and Biological Evaluation of Aromatase Inhibitors Based on Sulfonates and Sulfonamides of Resveratrol
inferred← citeshttps://doi.org/10.3390/ph16050718openalex-snapshot
Identification of Pinosylvin in Pinus nigra subsp. laricio: A Naturally Occurring Stilbenoid Suppressing LPS-Induced Expression of Pro-Inflammatory Cytokines and Mediators and Inhibiting the JAK/STAT Signaling Pathway
inferred← citeshttps://doi.org/10.3390/ph17081012openalex-snapshot
Cytotoxicity of Benzofuran-Containing Simplified Viniferin Analogues
inferred← citeshttps://doi.org/10.3390/ph17111482openalex-snapshot
Synthesis and Evaluation of Glucosyl-, Acyl- and Silyl- Resveratrol Derivatives as Retinoprotective Agents: Piceid Octanoate Notably Delays Photoreceptor Degeneration in a Retinitis Pigmentosa Mouse Model
inferred← citeshttps://doi.org/10.3390/plants12162935openalex-snapshot
Resveratrol and Other Natural Oligomeric Stilbenoid Compounds and Their Therapeutic Applications
inferred← citeshttps://doi.org/10.37349/eds.2025.1008106openalex-snapshot
Natural products targeting cancer stem cells: a promising therapeutic approach
inferred← citeshttps://doi.org/10.46572/nat.2020.5openalex-snapshot
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inferred← citeshttps://doi.org/10.5772/intechopen.1010264openalex-snapshot
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inferred← citeshttps://doi.org/10.58837/chula.the.2019.419openalex-snapshot
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inferred← citeshttps://doi.org/10.70675/8a58e2d5zf3e4z47b0za950z65e5510026feopenalex-snapshot
Impact de la Détente Instantanée Contrôlée (DIC) sur l’extraction des molécules bioactives de rhizomes de Rheum ribes L.
inferred← citeshttps://doi.org/10.7324/japs.2023.99205openalex-snapshot
3′-Hydroxypterostilbene and pinostilbene: Their chemistry, sources, anticancer and other pharmacological properties, pharmacokinetics, and patents
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