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Terpenoids from Euphorbia soongarica and Their Multidrug Resistance Reversal Activity

https://doi.org/10.1021/acs.jnatprod.6b01099

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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/ejoc.201200733openalex-snapshot

Diterpenes from European Euphorbia Species Serving as Prototypes for Natural‐Product‐Based Drug Discovery

inferredcites →https://doi.org/10.1016/0031-9422(92)80136-3openalex-snapshot

Diterpenoids from Euphorbia micractina

inferredcites →https://doi.org/10.1016/0031-9422(94)00587-jopenalex-snapshot

Diterpenoids from Euphorbia micractina

inferredcites →https://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

inferredcites →https://doi.org/10.1016/j.fitote.2015.11.009openalex-snapshot

New triterpenoids from the latex of Euphorbia resinifera Berg.

inferredcites →https://doi.org/10.1016/j.phymed.2009.07.009openalex-snapshot

Antitumor activity of terpenoids against classical and atypical multidrug resistant cancer cells

inferredcites →https://doi.org/10.1016/j.phytochem.2015.12.003openalex-snapshot

Diterpenoid constituents of Euphorbia macrorrhiza

inferredcites →https://doi.org/10.1016/s0040-4039(00)93940-6openalex-snapshot

The structure of new lathyrane diterpenes, jolkinols a, b, c, and d, from Euphorbia jolkini boiss.

inferredcites →https://doi.org/10.1021/cr078350sopenalex-snapshot

Chemical and Pharmacological Research of the Plants in Genus Euphorbia

inferredcites →https://doi.org/10.1021/cr400541jopenalex-snapshot

Euphorbia Diterpenes: Isolation, Structure, Biological Activity, and Synthesis (2008–2012)

inferredcites →https://doi.org/10.1021/np020508aopenalex-snapshot

New Sesquiterpenes from Litsea verticillata

inferredcites →https://doi.org/10.1021/np0205396openalex-snapshot

Euphane and Tirucallane Triterpenes from the Roots of Euphorbia kansui and Their in Vitro Effects on the Cell Division of Xenopus

inferredcites →https://doi.org/10.1021/np2001489openalex-snapshot

Lathyrane Diterpenoids from the Roots of Euphorbia micractina and Their Biological Activities

inferredcites →https://doi.org/10.1021/np300799nopenalex-snapshot

Jatropholane-Type Diterpenes from Euphorbia sikkimensis

inferredcites →https://doi.org/10.1021/np400029dopenalex-snapshot

Diterpenoids with Diverse Skeletons from the Roots of Euphorbia micractina

inferredcites →https://doi.org/10.1021/np50078a003openalex-snapshot

Structure Elucidation of Helioscopinolides D and E from Euphorbia calyptrata Cell Cultures

inferredcites →https://doi.org/10.1021/np900305jopenalex-snapshot

Chemical Constituents of the Roots of Euphorbia micractina

inferredcites →https://doi.org/10.1021/np960127vopenalex-snapshot

Identification of New Diterpenoids from Euphorbia calyptrata Cell Cultures

inferredcites →https://doi.org/10.1021/ol062854fopenalex-snapshot

Lagaspholones A and B: Two New Jatropholane-Type Diterpenes from Euphorbia lagascae

inferredcites →https://doi.org/10.1039/c4np00008kopenalex-snapshot

Biologically active diterpenes containing a gem-dimethylcyclopropane subunit: an intriguing source of PKC modulators

inferredcites →https://doi.org/10.1055/s-0034-1383244openalex-snapshot

Diterpenes from Euphorbia piscatoria: Synergistic Interaction of Lathyranes with Doxorubicin on Resistant Cancer Cells

inferredcites →https://doi.org/10.1055/s-2004-815542openalex-snapshot

Euphopubescenol and Euphopubescene, Two New Jatrophane Polyesters, and Lathyrane-type Diterpenes fromEuphorbia pubescens

inferredcites →https://doi.org/10.1055/s-2006-959583openalex-snapshot

Lathyrane and Ingenane Diterpenoids fromEuphorbia micractina

inferredcites →https://doi.org/10.1080/10286020802436016openalex-snapshot

Coumarin glycosides from Euphorbia soongarica (Boiss)

inferredcites →https://doi.org/10.1248/cpb.42.1101openalex-snapshot

Five D: C-Friedo-Oleanane Triterpenes from the Seeds of Trichosanthes kirilowii MAXIM. and Their Anti-inflammatory Effects.

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.2021.112846zenodo-depositor-declared

Diterpenoids from the genus Euphorbia: Structure and biological activity (2013–2019)

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113199zenodo-depositor-declared

Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113523zenodo-depositor-declared

Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities

inferred← citeshttps://doi.org/10.1002/ange.201906213openalex-snapshot

Synthesis of Functionalized α‐Vinyl Aldehydes from Enaminones

inferred← citeshttps://doi.org/10.1002/anie.201906213openalex-snapshot

Synthesis of Functionalized α‐Vinyl Aldehydes from Enaminones

inferred← citeshttps://doi.org/10.1002/ejoc.70589openalex-snapshot

A Comprehensive Synthetic Exploration of Euolutchuols A, B, C, and D, Hinokiol, and Related Abietane Diterpenoids

inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105689openalex-snapshot

Triterpenoids and meroterpenoids from the edible Ganoderma resinaceum and their potential anti-inflammatory, antioxidant and anti-apoptosis activities

inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106329openalex-snapshot

Synthesis, antiproliferative and anti-MDR activities of lathyrane diterpene derivatives based on configuration inversion strategy

inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107915openalex-snapshot

Structurally diverse triterpenoids with antibacterial activities from Euphorbia humifusa

inferred← citeshttps://doi.org/10.1016/j.bse.2025.104952openalex-snapshot

Chemical constituents of Euphorbia lathyris and their chemotaxonomic significance

inferred← citeshttps://doi.org/10.1016/j.bse.2025.105145openalex-snapshot

Sesquiterpenoids from the aerial parts of Hypericum lancasteri (Hypericaceae) and their chemotaxonomic significance

inferred← citeshttps://doi.org/10.1016/j.engmic.2022.100058openalex-snapshot

Sustainable biosynthesis of valuable diterpenes in microbes

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.02.026openalex-snapshot

New isopimarane diterpenes and nortriterpene with cytotoxic activity from Ephorbia alatavica Boiss

inferred← citeshttps://doi.org/10.1016/j.fitote.2019.01.015openalex-snapshot

Lewis acid-mediated skeleton transformation of Euphorbia diterpenes: From lathyrane to euphoractane and myrsinane

inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104989openalex-snapshot

Ten new nortriterpenes from Euphorbia resinifera and their anti-tomato yellow leaf curl virus activities

inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106405openalex-snapshot

Terpenoids and steroids from the whole plants of Euphorbia wallichii and their protective effects on STZ-induced damage in INS-1 cells

inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106725openalex-snapshot

Terpenoids from Euphorbia wallichii and their anti-inflammatory therapeutic potential

inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107119openalex-snapshot

New terpenoids from Euphorbia pekinensis with potent and selective anti-hepatocellular carcinoma activity

inferred← citeshttps://doi.org/10.1016/j.jep.2022.115574openalex-snapshot

Phytochemical and pharmacological review of diterpenoids from the genus Euphorbia Linn (2012–2021)

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113444openalex-snapshot

Jatrophane diterpenoids from Euphorbia microcarpa (prokh.) krylov with multidrug resistance modulating activity

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114148openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114257openalex-snapshot

Recent progress on triterpenoid derivatives and their anticancer potential

inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151303openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00249openalex-snapshot

Euphnerins A and B, Diterpenoids with a 5/6/6 Rearranged Spirocyclic Carbon Skeleton from the Stems of Euphorbia neriifolia

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00730openalex-snapshot

Euphane and Tirucallane Triterpenes with Trypanocidal Activity from Euphorbia desmondii

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b01025openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00134openalex-snapshot

Bioactive Diterpenoids from the Stems of Euphorbia antiquorum

inferred← citeshttps://doi.org/10.1021/acs.joc.7b02012openalex-snapshot

Synthesis of Homoverrucosanoid-Derived Esters and Evaluation as MDR Modulators

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Regio- and Diastereodivergent [4 + 2] Cycloadditions with Cyclic 2,4-Dienones

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/acscatal.2c03777openalex-snapshot

Rhodium/Amine Dual Catalytic System for Reassembling C≡C Bonds of Conjugated Alkynes with Cyclopropenes via Cutting/Insertion Cascade

inferred← citeshttps://doi.org/10.1039/c8np00079dopenalex-snapshot

Diterpenoids of terrestrial origin

inferred← citeshttps://doi.org/10.1039/d2np00047dopenalex-snapshot

Euphorbia diterpenoids: isolation, structure, bioactivity, biosynthesis, and synthesis (2013–2021)

inferred← citeshttps://doi.org/10.1039/d2ob01769eopenalex-snapshot

Combined photoredox/engineered P450 enzymatic direct dioxygen-functionalization of arylalkanes to chiral acyloins

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Profiling of euphane and tirucallane triterpenes from Euphorbia systyloides on antichagasic activity reveals antileukemia and immunomodulatory effects

inferred← citeshttps://doi.org/10.1080/14786419.2025.2459810openalex-snapshot

Triterpenoids from leaves of Paramignya trimera with their alpha-glucosidase inhibition: in vitro and in silico aspects

inferred← citeshttps://doi.org/10.1080/14786419.2026.2663132openalex-snapshot

Terpenoids from Euphorbia ebracteolata (Hayata.) with their multidrug resistance reversal activity

inferred← citeshttps://doi.org/10.1186/s10086-021-01947-xopenalex-snapshot

Extractives elucidation of Taiwania cryptomerioides sapwood

inferred← citeshttps://doi.org/10.3389/fphar.2020.00397openalex-snapshot

Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes

inferred← citeshttps://doi.org/10.3389/fphar.2021.648407openalex-snapshot

Clinically-Relevant ABC Transporter for Anti-Cancer Drug Resistance

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/ijms26010412openalex-snapshot

Study on the Chemical Composition and Multidrug Resistance Reversal Activity of Euphorbia uralensis (Euphorbiaceae)

inferred← citeshttps://doi.org/10.3390/molecules25174019openalex-snapshot

A Review of the Ethnomedicinal Uses, Biological Activities, and Triterpenoids of Euphorbia Species

inferred← citeshttps://doi.org/10.3390/plants12244181openalex-snapshot

LC-ESI QToF MS Non-Targeted Screening of Latex Extracts of Euphorbia seguieriana ssp. seguieriana Necker and Euphorbia cyparissias and Determination of Their Potential Anticancer Activity

inferred← citeshttps://doi.org/10.37349/emed.2023.00166openalex-snapshot

Mechanistic insights on anticancer drugs with specific biological targets and signalling pathways

inferred← citeshttps://doi.org/10.5772/intechopen.1010654openalex-snapshot

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inferred← citeshttps://doi.org/10.70675/d535d4f6ze297z4e33z965az6b622a16f280openalex-snapshot

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