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Antineoplastic Agents. 579. Synthesis and Cancer Cell Growth Evaluation of E-Stilstatin 3: A Resveratrol Structural Modification

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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/jnr.21503openalex-snapshot

Resveratrol and quercetin, two natural polyphenols, reduce apoptotic neuronal cell death induced by neuroinflammation

inferredcites →https://doi.org/10.1007/bf01954881openalex-snapshot

Isolation and structure of the strong cell growth and tubulin inhibitor combretastatin A-4

inferredcites →https://doi.org/10.1016/0040-4039(95)02294-5openalex-snapshot

A simple, rapid and efficient protocol for the selective phosphorylation of phenols with dibenzyl phosphite

inferredcites →https://doi.org/10.1016/0140-6736(93)92472-6openalex-snapshot

Inhibition of human LDL oxidation by resveratrol

inferredcites →https://doi.org/10.1016/j.bcp.2004.12.001openalex-snapshot

Antioxidant, prooxidant and cytotoxic activity of hydroxylated resveratrol analogues: structure–activity relationship

inferredcites →https://doi.org/10.1016/j.bmc.2007.06.030openalex-snapshot

‘Bridged’ stilbene derivatives as selective cyclooxygenase-1 inhibitors

inferredcites →https://doi.org/10.1016/j.canlet.2005.01.031openalex-snapshot

Resveratrol induces apoptosis and inhibits angiogenesis in human breast cancer xenografts in vivo

inferredcites →https://doi.org/10.1016/j.cmet.2007.08.014openalex-snapshot

SIRT1 Improves Insulin Sensitivity under Insulin-Resistant Conditions by Repressing PTP1B

inferredcites →https://doi.org/10.1016/j.lfs.2004.10.039openalex-snapshot

Toxicogenomics of resveratrol in rat liver

inferredcites →https://doi.org/10.1016/j.mrrev.2007.08.004openalex-snapshot

Resveratrol and its analogs: Defense against cancer, coronary disease and neurodegenerative maladies or just a fad?

inferredcites →https://doi.org/10.1016/j.phrs.2008.03.002openalex-snapshot

Combretastatin A-4 activates AMP-activated protein kinase and improves glucose metabolism in db/db mice

inferredcites →https://doi.org/10.1016/j.tet.2005.10.083openalex-snapshot

Synthesis of the 5-hydroxymethyl-6-aryl-8-oxabicyclo[3.2.1]oct-3-en-2-one natural products descurainin and cartorimine

inferredcites →https://doi.org/10.1016/s0008-6363(00)00102-4openalex-snapshot

Cardioprotective effect of resveratrol, a natural antioxidant derived from grapes

inferredcites →https://doi.org/10.1016/s0957-4166(02)00482-2openalex-snapshot

First enantioselective synthesis of daphneticin and its regioisomer

inferredcites →https://doi.org/10.1021/ja01070a002openalex-snapshot

Mechanisms of Photochemical Reactions in Solution. XXII.1 Photochemical cis-trans Isomerization

inferredcites →https://doi.org/10.1021/jm00010a011openalex-snapshot

Antineoplastic Agents. 291. Isolation and Synthesis of Combretastatins A-4, A-5, and A-6

inferredcites →https://doi.org/10.1021/jm010119yopenalex-snapshot

Antineoplastic Agents. 465. Structural Modification of Resveratrol: Sodium Resverastatin Phosphate

inferredcites →https://doi.org/10.1021/jm020204lopenalex-snapshot

Antineoplastic Agents. 487. Synthesis and Biological Evaluation of the Antineoplastic Agent 3,4-Methylenedioxy-5,4‘-dimethoxy-3‘-amino-Z-stilbene and Derived Amino Acid Amides

inferredcites →https://doi.org/10.1021/jm0205797openalex-snapshot

Antineoplastic Agents. 445. Synthesis and Evaluation of Structural Modifications of (Z)- and (E)-Combretastatin A-4

inferredcites →https://doi.org/10.1021/jm701362mopenalex-snapshot

Synthesis and Biological Activity of Fluorinated Combretastatin Analogues

inferredcites →https://doi.org/10.1021/jo00218a032openalex-snapshot

Antineoplastic agents. 113. Synthesis of natural (-)-combretastatin

inferredcites →https://doi.org/10.1021/np50049a016openalex-snapshot

Isolation, Structure, and Synthesis of Combretastatins A-1 and B-1, Potent New Inhibitors of Microtubule Assembly, Derived from Combretum caffrum

inferredcites →https://doi.org/10.1021/np800608copenalex-snapshot

Antineoplastic Agents. 578. Synthesis of Stilstatins 1 and 2 and Their Water-Soluble Prodrugs

inferredcites →https://doi.org/10.1038/nature01960openalex-snapshot

Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan

inferredcites →https://doi.org/10.1038/nature02789openalex-snapshot

Sirtuin activators mimic caloric restriction and delay ageing in metazoans

inferredcites →https://doi.org/10.1038/nrd2060openalex-snapshot

Therapeutic potential of resveratrol: the in vivo evidence

inferredcites →https://doi.org/10.1038/sj.bjp.0704637openalex-snapshot

The protective effect of resveratrols on ischaemia‐reperfusion injuries of rat hearts is correlated with antioxidant efficacy

inferredcites →https://doi.org/10.1039/b306797copenalex-snapshot

Combretastatins: from natural products to drug discovery

inferredcites →https://doi.org/10.1042/cs0980537openalex-snapshot

Resveratrol induces vasorelaxation of mesenteric and uterine arteries from female guinea-pigs

inferredcites →https://doi.org/10.1055/s-2008-1074516openalex-snapshot

Resveratrol from Red Grapes – Pedestrian Polyphenol or Useful Anticancer Agent?

inferredcites →https://doi.org/10.1124/dmd.104.000885openalex-snapshot

HIGH ABSORPTION BUT VERY LOW BIOAVAILABILITY OF ORAL RESVERATROL IN HUMANS

inferredcites →https://doi.org/10.1124/jpet.107.124966openalex-snapshot

Combretastatin A4-Induced Differential Cytotoxicity and Reduced Metastatic Ability by Inhibition of AKT Function in Human Gastric Cancer Cells

inferredcites →https://doi.org/10.1126/science.275.5297.218openalex-snapshot

Cancer Chemopreventive Activity of Resveratrol, a Natural Product Derived from Grapes

inferredcites →https://doi.org/10.1139/v82-202openalex-snapshot

Isolation and structure of combretastatin

inferredcites →https://doi.org/10.1139/v87-399openalex-snapshot

Isolation, structure, and synthesis of combretastatin A-2, A-3, and B-2

inferredcites →https://doi.org/10.1152/ajpheart.01065.2005openalex-snapshot

Acute responses to phytoestrogens in small arteries from men with coronary heart disease

inferredcites →https://doi.org/10.1158/1078-0432.ccr-03-0105openalex-snapshot

Resveratrol Suppresses the Angiogenesis and Tumor Growth of Gliomas in Rats

inferredcites →https://doi.org/10.1248/cpb.53.1587openalex-snapshot

Synthesis and Anti-inflammatory Activity of Resveratrol Analogs

inferredcites →https://doi.org/10.2174/092986708785132951openalex-snapshot

Trans-Resveratrol: A Magical Elixir of Eternal Youth?

inferredcites →https://doi.org/10.3184/030823408x324751openalex-snapshot

Synthesis of Combretastatin A-4 and Erianin

inferredcites →https://doi.org/10.3748/wjg.v11.i30.4745openalex-snapshot

Resveratrol prolongs allograft survival after liver transplantation in rats

inferredcites →https://doi.org/10.3892/ijmm.9.1.77openalex-snapshot

Effects of red wine and wine polyphenol resveratrol on platelet aggregation in vivo and in vitro

What points at this work

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

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Phytochemical Investigation on Trichilia Elegans a. Juss (Meliaceae) and its Chemotaxonomic Significance

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Phosphorus Ylides and Related Compounds

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Self‐Immolative Polymers Derived from Renewable Resources via Thiol–Ene Chemistry**

inferred← citeshttps://doi.org/10.1002/anie.202420054openalex-snapshot

Self‐Immolative Polymers Derived from Renewable Resources via Thiol–Ene Chemistry**

inferred← citeshttps://doi.org/10.1002/chem.201002020openalex-snapshot

Hybrid‐Increased Radical‐Scavenging Activity of Resveratrol Derivatives by Incorporating a Chroman Moiety of Vitamin E

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/10.1007/s11172-011-0304-7openalex-snapshot

Synthesis of hydrophilic and lipophilic 4-arylcoumarin phosphates

inferred← citeshttps://doi.org/10.1016/j.bmc.2013.09.064openalex-snapshot

Synthesis of combretastatin A-4 O-alkyl derivatives and evaluation of their cytotoxic, antiangiogenic and antitelomerase activity

inferred← citeshttps://doi.org/10.1016/j.bse.2013.03.017openalex-snapshot

Chemical constituents of Pholidota leveilleana

inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.05.048openalex-snapshot

Anticancer activity of ruthenium(II) arene complexes bearing 1,2,3,4-tetrahydroisoquinoline amino alcohol ligands

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2011.02.028openalex-snapshot

Finding more active antioxidants and cancer chemoprevention agents by elongating the conjugated links of resveratrol

inferred← citeshttps://doi.org/10.1016/j.phytol.2014.08.003openalex-snapshot

Caryolane-type sesquiterpenes from Cirsium souliei

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00691openalex-snapshot

Constituents of Fagraea fragrans with Antimycobacterial Activity in Combination with Erythromycin

inferred← citeshttps://doi.org/10.1021/np200797xopenalex-snapshot

Antineoplastic Agents. 548. Synthesis of Iodo- and Diiodocombstatin Phosphate Prodrugs

inferred← citeshttps://doi.org/10.1021/np9004486openalex-snapshot

An Efficient Synthetic Strategy for Obtaining 4-Methoxy Carbon Isotope Labeled Combretastatin A-4 Phosphate and Other Z-Combretastatins

inferred← citeshttps://doi.org/10.1039/bk9781849731386-00074openalex-snapshot

Phosphonium salts and P-ylides

inferred← citeshttps://doi.org/10.1039/c3ob40420jopenalex-snapshot

Scope and limitations of the Heck–Matsuda-coupling of phenol diazonium salts and styrenes: a protecting-group economic synthesis of phenolic stilbenes

inferred← citeshttps://doi.org/10.1039/c6ra22026fopenalex-snapshot

Anti selective glycolate aldol reactions of (S)-4-isopropyl-1-[(R)-1-phenylethyl]imidazolidin-2-one: application towards the asymmetric synthesis of 8-4′-oxyneolignans

inferred← citeshttps://doi.org/10.1080/07391102.2021.1910572openalex-snapshot

Molecular insights into a mechanism of resveratrol action using hybrid computational docking/CoMFA and machine learning approach

inferred← citeshttps://doi.org/10.1201/b11196-10openalex-snapshot

From Natural Polyphenols to Synthetic Antitumor Agents

inferred← citeshttps://doi.org/10.1515/ncrs-2022-0079openalex-snapshot

Crystal structure of (E)-1-(4-(3,5-dimethoxystyryl)phenyl)-7-ethylheptanedioate, C25H30O6

inferred← citeshttps://doi.org/10.3109/14756366.2014.979347openalex-snapshot

Design and synthesis of resveratrol–salicylate hybrid derivatives as CYP1A1 inhibitors

inferred← citeshttps://doi.org/10.3390/molecules17077989openalex-snapshot

Flavonoids and Other Compounds from Ouratea ferruginea (Ochnaceae) as Anticancer and Chemopreventive Agents

inferred← citeshttps://doi.org/10.3390/molecules23020472openalex-snapshot

Bioactive Phenolic and Isocoumarin Glycosides from the Stems of Homalium paniculiflorum

inferred← citeshttps://doi.org/10.3892/ol.2017.5982openalex-snapshot

Anti‑proliferative and anti‑metastasis effects of ten oligostilbenes from the seeds of Paeonia suffruticosa on human cancer cells

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