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12,17-Cyclojatrophane and Jatrophane Constituents of Euphorbia welwitschii

https://doi.org/10.1021/acs.jnatprod.5b00631

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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/10.1007/s11101-009-9126-8openalex-snapshot

Jatrophane diterpenes from Euphorbia spp. as modulators of multidrug resistance in cancer therapy

inferredcites →https://doi.org/10.1007/s11101-014-9342-8openalex-snapshot

Euphorbia and Momordica metabolites for overcoming multidrug resistance

inferredcites →https://doi.org/10.1016/0031-9422(89)80360-7openalex-snapshot

Diterpenes from Euphorbia helioscopia

inferredcites →https://doi.org/10.1016/j.bmc.2014.05.006openalex-snapshot

Macrocyclic diterpenes resensitizing multidrug resistant phenotypes

inferredcites →https://doi.org/10.1016/j.bmc.2014.09.041openalex-snapshot

Improving the MDR reversal activity of 6,17-epoxylathyrane diterpenes

inferredcites →https://doi.org/10.1016/j.ejps.2012.11.012openalex-snapshot

QSAR studies of macrocyclic diterpenes with P-glycoprotein inhibitory activity

inferredcites →https://doi.org/10.1016/j.tips.2009.07.003openalex-snapshot

Is resistance useless? Multidrug resistance and collateral sensitivity

inferredcites →https://doi.org/10.1016/s0031-9422(97)00832-7openalex-snapshot

Diterpenes from Euphorbia paralias

inferredcites →https://doi.org/10.1016/s0040-4039(01)01285-0openalex-snapshot

Salicifoline and salicinolide, new diterpene polyesters from Euphorbia salicifolia

inferredcites →https://doi.org/10.1016/s0378-8741(00)00341-xopenalex-snapshot

Plants used against cancer – an extension of the work of Jonathan Hartwell

inferredcites →https://doi.org/10.1021/ci200145popenalex-snapshot

Toward a Better Pharmacophore Description of P-Glycoprotein Modulators, Based on Macrocyclic Diterpenes fromEuphorbiaSpecies

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/jm301441wopenalex-snapshot

Enhancing Macrocyclic Diterpenes as Multidrug-Resistance Reversers: Structure–Activity Studies on Jolkinol D Derivatives

inferredcites →https://doi.org/10.1021/np010015qopenalex-snapshot

New Jatrophane Diterpenoid Esters from Euphorbia turczaninowii

inferredcites →https://doi.org/10.1021/np0706163openalex-snapshot

Cytotoxic Diterpenoids from Euphorbia helioscopia

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/np3004003openalex-snapshot

Jatrophane Diterpenes fromEuphorbia melliferaand Their Activity as P-Glycoprotein Modulators on Multidrug-Resistant Mouse Lymphoma and Human Colon Adenocarcinoma Cells

inferredcites →https://doi.org/10.1246/bcsj.58.3112openalex-snapshot

Isolation and Structures of Euphohelins, New Toxic Diterpenes from Euphorbia Helioscopia L.

inferredcites →https://doi.org/10.2174/187152012803529655openalex-snapshot

Colon Adenocarcinoma Multidrug Resistance Reverted by Euphorbia Diterpenes: Structure-Activity Relationships and Pharmacophore Modeling

inferredcites →https://doi.org/10.5897/jmpr.9001294openalex-snapshot

Why do Euphorbiaceae tick as medicinal plants? A review of Euphorbiaceae family and its medicinal features

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/10.1007/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/b978-0-12-817905-5.00009-3openalex-snapshot

Jatrophane diterpenes from Euphorbiaceae family

inferred← citeshttps://doi.org/10.1016/j.apsb.2018.03.011openalex-snapshot

Helioscopianoids A–Q, bioactive jatrophane diterpenoid esters from Euphorbia helioscopia

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.phymed.2016.05.007openalex-snapshot

Jatrophane diterpenes and cancer multidrug resistance – ABCB1 efflux modulation and selective cell death induction

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01087openalex-snapshot

Studies of Jatrogossone A as a Reactive Oxygen Species Inducer in Cancer Cellular Models

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00929openalex-snapshot

Jatrophane Diterpenoids from Euphorbia esula as Inhibitors of RANKL-Induced Osteoclastogenesis

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00787openalex-snapshot

Three Minor Diterpenoids with Three Carbon Skeletons from Euphorbia peplus

inferred← citeshttps://doi.org/10.1021/jacs.5c21832openalex-snapshot

CrystalX: High-Accuracy Crystal Structure Analysis Using Deep Learning

inferred← citeshttps://doi.org/10.1038/s41598-017-04399-wopenalex-snapshot

Heliosterpenoids A and B, two Novel Jatrophane-Derived Diterpenoids with a 5/6/4/6 Ring System from Euphorbia helioscopia

inferred← citeshttps://doi.org/10.1039/c6np00059bopenalex-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/10.3389/fphar.2020.00599openalex-snapshot

Epoxylathyrane Derivatives as MDR-Selective Compounds for Disabling Multidrug Resistance in Cancer

inferred← citeshttps://doi.org/10.3390/molecules27238307openalex-snapshot

Efforts in Bioprospecting Research: A Survey of Novel Anticancer Phytochemicals Reported in the Last Decade

inferred← citeshttps://doi.org/10.4155/fmc-2017-0228openalex-snapshot

Optimizing the Flavanone Core Toward New Selective Nitrogen-Containing Modulators of ABC Transporters

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