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Discovery and Biological Evaluation of a New Family of Potent Modulators of Multidrug Resistance: Reversal of Multidrug Resistance of Mouse Lymphoma Cells by New Natural Jatrophane Diterpenoids Isolated from Euphorbia Species

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What this work says

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

inferredcites →https://doi.org/10.1016/0031-9422(89)80360-7openalex-snapshot
Diterpenes from Euphorbia helioscopia
inferredcites →https://doi.org/10.1016/s0021-9258(18)61633-3openalex-snapshot
Certain calcium channel blockers bind specifically to multidrug-resistant human KB carcinoma membrane vesicles and inhibit drug binding to P-glycoprotein.
inferredcites →https://doi.org/10.1016/s0031-9422(00)98551-0openalex-snapshot
A diterpene from Euphorbia maddeni
inferredcites →https://doi.org/10.1016/s0031-9422(97)00749-8openalex-snapshot
Jatrophane diterpenoids from Euphorbia esula
inferredcites →https://doi.org/10.1016/s0031-9422(99)00088-6openalex-snapshot
Jatrophane diterpenoids from Euphorbia peplus
inferredcites →https://doi.org/10.1016/s0040-4020(00)00278-7openalex-snapshot
Serrulatin A and B, New Diterpene Polyesters from Euphorbia serrulata
inferredcites →https://doi.org/10.1016/s0040-4020(00)00982-0openalex-snapshot
Euphosalicin, a new diterpene polyester with multidrug resistance reversing activity from Euphorbia salicifolia
inferredcites →https://doi.org/10.1021/np960669copenalex-snapshot
Macrocyclic Diterpene Polyesters of the Jatrophane Type from Euphorbia esula
inferredcites →https://doi.org/10.1021/np970507wopenalex-snapshot
Macrocyclic Diterpenoids from Euphorbia semiperfoliata
inferredcites →https://doi.org/10.1080/09687680010030200openalex-snapshot
Multidrug transporters in prokaryotic and eukaryotic cells: physiological functions and transport mechanisms
inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot
On enantiomorph-polarity estimation
inferredcites →https://doi.org/10.2172/369685openalex-snapshot
ORTEP-III: Oak Ridge Thermal Ellipsoid Plot Program for crystal structure illustrations

What points at this work

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

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Bond reactivity indices approach analysis of the [2+2] cycloaddition of jatrophane skeleton diterpenoids from Euphorbia gaditana Coss to tetracyclic gaditanone
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Diterpene Constituents of Euphorbia exigua L. and Multidrug Resistance Reversing Activity of the Isolated Diterpenes
inferred← citeshttps://doi.org/10.1002/cbdv.202200660openalex-snapshot
New Jatrophane‐Type Diterpenoids from Euphorbia kansui as Potential MDR Reversal Agents
inferred← citeshttps://doi.org/10.1002/chin.200238184openalex-snapshot
Discovery and Biological Evaluation of a New Family of Potent Modulators of Multidrug Resistance: Reversal of Multidrug Resistance of Mouse Lymphoma Cells by New Natural Jatrophane Diterpenoids (I)‐(III) Isolated from Euphorbia Species.
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Diterpenes from European Euphorbia Species Serving as Prototypes for Natural‐Product‐Based Drug Discovery
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Isolation and Structural Characterization of New, Highly Functionalized Diterpenes from Euphorbia serrulata
inferred← citeshttps://doi.org/10.1002/hlca.200390282openalex-snapshot
Isolation and Structure Determination of New Jatrophane Diterpenoids from Euphorbia platyphyllos L.
inferred← citeshttps://doi.org/10.1002/hlca.200590124openalex-snapshot
Toward a Total Synthesis of Macrocyclic Jatrophane Diterpenes – Concise Route to a Highly Functionalized Cyclopentane Key Intermediate
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Euphorbiasteroid reverses P‐glycoprotein‐mediated multi‐drug resistance in human sarcoma cell line MES‐SA/Dx5
inferred← citeshttps://doi.org/10.1007/978-981-16-4779-6_13openalex-snapshot
Role of Plant Secondary Metabolites as Modulators of Multidrug Resistance in Cancer Therapy
inferred← citeshttps://doi.org/10.1007/s00432-006-0084-xopenalex-snapshot
Induction of apoptosis in leukemia cell lines by Linum persicum and Euphorbia cheiradenia
inferred← citeshttps://doi.org/10.1007/s10886-006-9079-yopenalex-snapshot
Efflux Transporters as a Novel Herbivore Countermechanism to Plant Chemical Defenses
inferred← citeshttps://doi.org/10.1007/s10886-006-9080-5openalex-snapshot
Is alpha-Pinene a Substrate for Permeability-Glycoprotein in Wood Rats?
inferred← citeshttps://doi.org/10.1007/s10886-006-9086-zopenalex-snapshot
Application of Pharmacological Approaches to Plant–Mammal Interactions
inferred← citeshttps://doi.org/10.1007/s11033-009-9558-7openalex-snapshot
Molecular cloning, characterization and function analysis of the gene encoding HMG-CoA reductase from Euphorbia Pekinensis Rupr
inferred← citeshttps://doi.org/10.1007/s11101-009-9126-8openalex-snapshot
Jatrophane diterpenes from Euphorbia spp. as modulators of multidrug resistance in cancer therapy
inferred← citeshttps://doi.org/10.1007/s11101-014-9342-8openalex-snapshot
Euphorbia and Momordica metabolites for overcoming multidrug resistance
inferred← citeshttps://doi.org/10.1007/s11101-020-09667-8openalex-snapshot
Jatrophane and rearranged jatrophane-type diterpenes: biogenesis, structure, isolation, biological activity and SARs (1984–2019)
inferred← citeshttps://doi.org/10.1016/b978-0-12-819541-3.00009-8openalex-snapshot
Potential for cancer treatment: natural products from the Balkans
inferred← citeshttps://doi.org/10.1016/b978-0-443-23932-8.00004-2openalex-snapshot
Discovery of lead compounds from pseudo-natural macrocycles enabled by modular biomimetic strategy
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.104989openalex-snapshot
Jatrophane diterpenoids as multidrug resistance modulators from Euphorbia sororia
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.09.028openalex-snapshot
Apoptosis induction and modulation of P-glycoprotein mediated multidrug resistance by new macrocyclic lathyrane-type diterpenoids
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.08.071openalex-snapshot
Synergistic interaction between p-glycoprotein modulators and epirubicine on resistant cancer cells
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.04.041openalex-snapshot
Lathyrane diterpenes from Euphorbia lathyris as modulators of multidrug resistance and their crystal structures
inferred← citeshttps://doi.org/10.1016/j.bmc.2025.118516openalex-snapshot
Biomimetic semi-synthesis, structural optimization and anti-HIV activity of naturally scarce eupholathone-, lathyranone- and integerrimine-type Euphorbia diterpenoids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2018.01.027openalex-snapshot
Jatrophane diterpenoids from Euphorbia sororia as potent modulators against P-glycoprotein-based multidrug resistance
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114822openalex-snapshot
Discovery of a novel highly potent and low-toxic jatrophane derivative enhancing the P-glycoprotein-mediated doxorubicin sensitivity of MCF-7/ADR cells
inferred← citeshttps://doi.org/10.1016/j.fct.2011.09.035openalex-snapshot
New anti-cancer characteristics of jatrophane diterpenes from Euphorbia dendroides
inferred← citeshttps://doi.org/10.1016/j.fitote.2010.10.015openalex-snapshot
Macrocyclic diterpenoids from the Iranian plant Euphorbia bungei Boiss.
inferred← citeshttps://doi.org/10.1016/j.fitote.2013.11.008openalex-snapshot
Jatrophane diterpenoid esters from Euphorbia sororia serving as multidrug resistance reversal agents
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106839openalex-snapshot
Jatrophane diterpenes from Euphorbia Sororia enhance chemotherapy drugs sensitivities in P-gp-induced multidrug resistance cells
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121629openalex-snapshot
Oxazolidinones as chiral auxiliaries in asymmetric aldol reaction applied to natural products total synthesis
inferred← citeshttps://doi.org/10.1016/j.molcatb.2017.02.008openalex-snapshot
Regioselective hydroxylation of lathyrane diterpenoids biocatalyzed by microorganisms and its application in integrated synthesis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127409openalex-snapshot
NMR and SC-XRD analyses of a solid solution of diastereomers of microphyllane diterpenoids from Salvia hirsuta
inferred← citeshttps://doi.org/10.1016/j.phymed.2018.02.001openalex-snapshot
Mechanism of action of cytotoxic compounds from the seeds of Euphorbia lathyris
inferred← citeshttps://doi.org/10.1016/j.phytochem.2005.06.008openalex-snapshot
Multidrug resistance reversal agent from Jatropha elliptica
inferred← citeshttps://doi.org/10.1016/j.phytochem.2006.06.030openalex-snapshot
Chemistry and biological activity of secondary metabolites in Euphorbia from Iran
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.09.003openalex-snapshot
Bioactive diterpenoids from Croton laevigatus
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.01.016openalex-snapshot
Jatrophane diterpenoids with multidrug-resistance modulating activity from the latex of Euphorbia nicaeensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113344openalex-snapshot
Ingol, ent-atisane, and stachane-type diterpenoids from Euphorbia deightonii with multidrug resistance reversing activity
inferred← citeshttps://doi.org/10.1016/j.tet.2004.04.028openalex-snapshot
New tri- and tetracyclic diterpenes from Euphorbia villosa
inferred← citeshttps://doi.org/10.1016/j.tet.2005.02.031openalex-snapshot
Amygdaloidins A–L, twelve new 13 α-OH jatrophane diterpenes from Euphorbia amygdaloides L.
inferred← citeshttps://doi.org/10.1016/j.tet.2011.07.051openalex-snapshot
New premyrsinane-type diterpene polyesters from Euphorbia falcata
inferred← citeshttps://doi.org/10.1016/j.tet.2012.07.101openalex-snapshot
Jatrophane diterpenoids with multidrug resistance-modulating activity from Euphorbia mongolica Prokh.
inferred← citeshttps://doi.org/10.1016/j.tet.2016.08.007openalex-snapshot
Jatrophane diterpenes from Euphorbia guyoniana are new potent inhibitors of atrial GIRK channels
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.09.099openalex-snapshot
Kansuinone, a novel euphane-type triterpene from Euphorbia kansui
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.2c01424openalex-snapshot
Modular Biomimetic Strategy Enabled Discovery of Simplified Pseudo-Natural Macrocyclic P-Glycoprotein Inhibitors Capable of Overcoming Multidrug Resistance
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b00058openalex-snapshot
Lathyrol Diterpenes as Modulators of P-Glycoprotein Dependent Multidrug Resistance: Structure–Activity Relationship Studies on Euphorbia Factor L 3 Derivatives
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.6b00605openalex-snapshot
Jatrophane Diterpenoids as Modulators of P-Glycoprotein-Dependent Multidrug Resistance (MDR): Advances of Structure–Activity Relationships and Discovery of Promising MDR Reversal Agents
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00370openalex-snapshot
Epoxylathyrol Derivatives: Modulation of ABCB1-Mediated Multidrug Resistance in Human Colon Adenocarcinoma and Mouse T-Lymphoma Cells
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00990openalex-snapshot
Evaluation of Jatrophane Esters from Euphorbia spp. as Modulators of Candida albicans Multidrug Transporters
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00332openalex-snapshot
Gaditanone, a Diterpenoid Based on an Unprecedented Carbon Skeleton Isolated from Euphorbia gaditana
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01114openalex-snapshot
Pepluanols C–D, Two Diterpenoids with Two Skeletons from Euphorbia peplus
inferred← citeshttps://doi.org/10.1021/cr078350sopenalex-snapshot
Chemical and Pharmacological Research of the Plants in Genus Euphorbia
inferred← citeshttps://doi.org/10.1021/cr400541jopenalex-snapshot
Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008–2012)
inferred← citeshttps://doi.org/10.1021/jm030787eopenalex-snapshot
Jatrophane Diterpenes as P-Glycoprotein Inhibitors. First Insights of Structure−Activity Relationships and Discovery of a New, Powerful Lead
inferred← citeshttps://doi.org/10.1021/jm030951yopenalex-snapshot
Jatrophane Diterpenes as Modulators of Multidrug Resistance. Advances of Structure−Activity Relationships and Discovery of the Potent Lead Pepluanin A
inferred← citeshttps://doi.org/10.1021/jo1019738openalex-snapshot
Total Synthesis of Natural and Non-Natural Δ5,6Δ12,13-Jatrophane Diterpenes and Their Evaluation as MDR Modulators
inferred← citeshttps://doi.org/10.1021/jo102033hopenalex-snapshot
Total Synthesis of Lathyranoic Acid A
inferred← citeshttps://doi.org/10.1021/np0203537openalex-snapshot
A New P-Glycoprotein Inhibitor from the Caper Spurge (Euphorbia lathyris)
inferred← citeshttps://doi.org/10.1021/np030036fopenalex-snapshot
Jatrophane Diterpenoids from Euphorbia m ongolica as Modulators of the Multidrug Resistance of L5128 Mouse Lymphoma Cells
inferred← citeshttps://doi.org/10.1021/np0400048openalex-snapshot
Bioactive Diterpenoids, a New Jatrophane and Two ent-Abietanes, and Other Constituents from Euphorbia pubescens
inferred← citeshttps://doi.org/10.1021/np0581216openalex-snapshot
Natural Product Extracts of Plant and Marine Origin Having Antileukemia Potential. The NCI Experience
inferred← citeshttps://doi.org/10.1021/np060046ropenalex-snapshot
Euphoportlandols A and B, Tetracylic Diterpene Polyesters from Euphorbia p ortlandica and Their Anti-MDR Effects in Cancer Cells
inferred← citeshttps://doi.org/10.1021/np200202hopenalex-snapshot
Jatrophane Diterpenes from Euphorbia esula as Antiproliferative Agents and Potent Chemosensitizers to Overcome Multidrug Resistance
inferred← citeshttps://doi.org/10.1021/np200241copenalex-snapshot
Isolation and Biological Evaluation of Jatrophane Diterpenoids from Euphorbia dendroides
inferred← citeshttps://doi.org/10.1021/np3004003openalex-snapshot
Jatrophane Diterpenes fromEuphorbia melliferaand Their Activity as P-Glycoprotein Modulators on Multidrug-Resistant Mouse Lymphoma and Human Colon Adenocarcinoma Cells
inferred← citeshttps://doi.org/10.1021/np500756zopenalex-snapshot
Jatrophanes from Euphorbia squamosa as Potent Inhibitors of Candida albicans Multidrug Transporters
inferred← citeshttps://doi.org/10.1021/ol060115topenalex-snapshot
Synthesis of the Norjatrophane Diterpene (−)-15-Acetyl-3-propionyl- 17-norcharaciol
inferred← citeshttps://doi.org/10.1021/ol062854fopenalex-snapshot
Lagaspholones A and B: Two New Jatropholane-Type Diterpenes from Euphorbia lagascae
inferred← citeshttps://doi.org/10.1046/j.1359-4117.2003.01067.xopenalex-snapshot
The reversal of multidrug resistance: an update
inferred← citeshttps://doi.org/10.1055/a-0589-0525openalex-snapshot
Bioactive Segetane, Ingenane, and Jatrophane Diterpenes from Euphorbia taurinensis
inferred← citeshttps://doi.org/10.1055/s-2007-993765openalex-snapshot
Three New Jatrophane Polyesters and Antiproliferative Constituents from Euphorbia tuckeyana
inferred← citeshttps://doi.org/10.1080/10496475.2012.734549openalex-snapshot
Phytochemical and Antibacterial Studies of Different Parts ofEuphorbia hirtaL.
inferred← citeshttps://doi.org/10.1086/378923openalex-snapshot
A Specialist Herbivore (Neotoma stephensi) Absorbs Fewer Plant Toxins than Does a Generalist (Neotoma albigula)
inferred← citeshttps://doi.org/10.1093/jac/dkl460openalex-snapshot
Bacterial efflux pump inhibitors from natural sources
inferred← citeshttps://doi.org/10.1107/s205698901901541xopenalex-snapshot
Crystal and molecular structure of jatrophane diterpenoid (2R,3R,4S,5R,7S,8S,9S,13S,14S,15R)-2,3,8,9-tetraacetoxy-5,14-bis(benzoyloxy)-15-hydroxy-7-(isobutanoyloxy)jatropha-6(17),11(E)-diene
inferred← citeshttps://doi.org/10.1139/y06-052openalex-snapshot
Protective effects of polysaccharide from Euphorbia kansui (Euphorbiaceae) on the swimming exercise-induced oxidative stress in mice
inferred← citeshttps://doi.org/10.1155/2015/879238openalex-snapshot
Study on Molecular Recognition between Euphorbia Factor L713283 and β ‐Tubulin via Molecular Simulation Methods
inferred← citeshttps://doi.org/10.1177/1934578x0800300629openalex-snapshot
Diterpenes from Euphorbia as Potential Leads for Drug Design
inferred← citeshttps://doi.org/10.1177/1934578x0900400426openalex-snapshot
The Chemical Composition of the Essential Oils of Euphorbia caracasana and E. Cotinifolia (Euphorbiaceae) from Venezuela
inferred← citeshttps://doi.org/10.1177/1934578x1300800115openalex-snapshot
Headspace, Solid-phase Micro-extraction, Gas Chromatographic-Mass Spectrometric Analysis of Terpenoids in the Latex of Euphorbia Species
inferred← citeshttps://doi.org/10.1177/1934578x19848168openalex-snapshot
Jatrophane Diterpenoids With Protective Effect on Human Lymphocytes DNA
inferred← citeshttps://doi.org/10.1201/b11196-13openalex-snapshot
Plant Compounds and Derivatives as Inhibitors of Cancer Cell Multidrug Resistance
inferred← citeshttps://doi.org/10.1211/jpp.60.2.0015openalex-snapshot
Cytotoxic activity of an octadecenoic acid extract from Euphorbia kansui (Euphorbiaceae) on human tumour cell strains
inferred← citeshttps://doi.org/10.1248/bpb.32.1053openalex-snapshot
Gallotannin Isolated from Euphorbia Species, 1,2,6-Tri-O-galloyl-.BETA.-D-allose, Decreases Nitric Oxide Production through Inhibition of Nuclear Factor-.KAPPA.>B and Downstream Inducible Nitric Oxide Synthase Expression in Macrophages
inferred← citeshttps://doi.org/10.1556/hmj.2.2008.2.28358openalex-snapshot
Perspectives in Cancer Chemotherapy, in vitro and in vivo Experiments
inferred← citeshttps://doi.org/10.1556/oh.2009.28358openalex-snapshot
Perspectives of inhibition of multidrug resistance during cancer chemotherapy, in vitro and in vivo experiments
inferred← citeshttps://doi.org/10.1590/s0102-695x2011005000096openalex-snapshot
The crude latex of Euphorbia tirucalli modulates the cytokine response of leukocytes, especially CD4+ T lymphocytes
inferred← citeshttps://doi.org/10.2174/1381612043383449openalex-snapshot
Imaging Drug Resistance with Radiolabeled Molecules
inferred← citeshttps://doi.org/10.2174/138161206775201893openalex-snapshot
Inhibition of Multidrug Resistance of Cancer Cells by Natural Diterpenes, Triterpenes and Carotenoids
inferred← citeshttps://doi.org/10.2174/138527212803520227openalex-snapshot
Recent Applications of the Horner-Wadsworth-Emmons Reaction to the Synthesis of Natural Products
inferred← citeshttps://doi.org/10.30616/ajb.1531295openalex-snapshot
Investigation of the effect of myrtle spurge (Euphorbia myrsinites L.) extract on some mechanical properties of fabrics
inferred← citeshttps://doi.org/10.3389/fmicb.2012.00130openalex-snapshot
Secondary Metabolites from Plants Inhibiting ABC Transporters and Reversing Resistance of Cancer Cells and Microbes to Cytotoxic and Antimicrobial Agents
inferred← citeshttps://doi.org/10.3389/fphar.2022.815603openalex-snapshot
Research Progress on Natural Diterpenoids in Reversing Multidrug Resistance
inferred← citeshttps://doi.org/10.3390/molecules31173024openalex-snapshot
Jatrophane Diterpenoids from Euphorbia peplus with LysoTracker-Associated Cellular Activity
inferred← citeshttps://doi.org/10.3762/bjoc.11.291openalex-snapshot
Genicunolide A, B and C: three new triterpenoids from Euphorbia geniculata
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