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Euphorhelipanes A and B, Triglyceride-Lowering Euphorbia Diterpenoids with a Bicyclo[4.3.0]nonane Core from Euphorbia helioscopia

https://doi.org/10.1021/acs.jnatprod.8b00780

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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/j.bioorg.2018.06.025openalex-snapshot

Cytotoxic macrocyclic diterpenoids from Jatropha multifida

inferredcites →https://doi.org/10.1016/j.phytochem.2017.09.003openalex-snapshot

Bioactive diterpenoids from Croton laevigatus

inferredcites →https://doi.org/10.1016/j.phytochem.2017.10.012openalex-snapshot

Highly oxygenated and structurally diverse diterpenoids from Euphorbia helioscopia

inferredcites →https://doi.org/10.1021/acs.jmedchem.5b01566openalex-snapshot

Synthesis and Biological Evaluation of Novel Bouchardatine Derivatives as Potential Adipogenesis/Lipogenesis Inhibitors for Antiobesity Treatment

inferredcites →https://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

inferredcites →https://doi.org/10.1021/acs.joc.7b02558openalex-snapshot

Secoheliosphanes A and B and Secoheliospholane A, Three Diterpenoids with Unusual seco-Jatrophane and seco-Jatropholane Skeletons from Euphorbia helioscopia

inferredcites →https://doi.org/10.1021/acs.orglett.8b01215openalex-snapshot

Heliojatrones A and B, Two Jatrophane-Derived Diterpenoids with a 5/10 Fused-Ring Skeleton from Euphorbia helioscopia: Structural Elucidation and Biomimetic Conversion

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/cr900386hopenalex-snapshot

Synthetic Applications of the Carbonyl Generating Grob Fragmentation

inferredcites →https://doi.org/10.1021/ja00995a057openalex-snapshot

Structure by nuclear magnetic resonance. XIV. Anisotropic effects of the carbonyl group

inferredcites →https://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

inferredcites →https://doi.org/10.1039/c0np00019aopenalex-snapshot

Two rings in them all: The labdane-related diterpenoids

inferredcites →https://doi.org/10.1039/c5np00137dopenalex-snapshot

Clerodane diterpenes: sources, structures, and biological activities

inferredcites →https://doi.org/10.1039/np9920900001openalex-snapshot

Diterpenoids

inferredcites →https://doi.org/10.1111/bph.13855openalex-snapshot

Natural alkaloid bouchardatine ameliorates metabolic disorders in high‐fat diet‐fed mice by stimulating the sirtuin 1/liver kinase B‐1/AMPK axis

inferredcites →https://doi.org/10.2174/1389557515666150511154108openalex-snapshot

Prostratin: An Overview

inferredcites →https://doi.org/10.2174/156802611796904924openalex-snapshot

Therapeutic Targeting of TRPV1 by Resiniferatoxin, from Preclinical Studies to Clinical Trials

inferredcites →https://doi.org/10.2310/7750.2012.12050openalex-snapshot

Ingenol Mebutate: A Promising Treatment for Actinic Keratoses and Nonmelanoma Skin Cancers

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.2020.112649zenodo-depositor-declared

Euphorbia helioscopia L.: A phytochemical and pharmacological overview

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/10.1002/cbdv.202301454openalex-snapshot

ent‐Atisane Diterpenoids from Euphorbia helioscopia and Their Anti‐inflammatory Activities

inferred← citeshttps://doi.org/10.1002/cjoc.202300275openalex-snapshot

Natural Sesquiterpenoids, Diterpenoids, Sesterterpenoids, and Triterpenoids with Intriguing Structures from 2017 to 2022

inferred← citeshttps://doi.org/10.1007/s00216-025-05893-1openalex-snapshot

Integrating metabolite-based molecular networking with database matching and LC-MS-guided targeted isolation for the discovery of novel chemical constituents: application to Euphorbia helioscopia L.

inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105534openalex-snapshot

Diterpenoids from Euphorbia helioscopia and their enhancement of NK cell-mediated killing of NSCLC cells

inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106103openalex-snapshot

Tigliane and rhamnofolane glycosides from Euphorbia wallichii prevent oxidative stress-induced neuronal death in PC-12 cells

inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105139openalex-snapshot

Euphzycopias A−I, macrocyclic diterpenes with NLRP3 inflammasome inhibitory activity from Euphorbia helioscopia L.

inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105614openalex-snapshot

Euphopias G − J, macrocyclic diterpenes with anti-zika virus activity from Euphorbia helioscopia L

inferred← citeshttps://doi.org/10.1016/j.fitote.2024.105821openalex-snapshot

Euphzycopins A − D, macrocyclic diterpenoids with potential anti-inflammatory activity from Euphorbia Helioscopia

inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106830openalex-snapshot

Lathyrane and jatrophane diterpenoids: Potential lipid-lowering agents from Euphorbia helioscopia L

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.2022.113420openalex-snapshot

Jatrophane diterpenoids with cytotoxic activity from the whole plant of Euphorbia heliosocpia L

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113425openalex-snapshot

Unprecedented diterpene skeletons isolated from vascular plants in the last twenty years (2001–2021)

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114313openalex-snapshot

ent-Abietane-type lactones with anti-inflammatory activity from Euphorbia helioscopia

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00879openalex-snapshot

Jatrophane Diterpenoids with Kv1.3 Ion Channel Inhibitory Effects from Euphorbia helioscopia

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00822openalex-snapshot

Discovery of Ingenane Diterpenoids from Euphorbia hylonoma as Antiadipogenic Agents

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00519openalex-snapshot

Macrocyclic Diterpenoids from Euphorbia helioscopia and Their Potential Anti-inflammatory Activity

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00634openalex-snapshot

19- nor -, 20- nor -, and tetranor -Halimane-Type Furanoditerpenoids from Croton crassifolius

inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04145openalex-snapshot

Diterpenoids with Rearranged 9(10→11)-abeo-10,12-Cyclojatrophane Skeleton and the First (15S)-Jatrophane from Euphorbia helioscopia: Structural Elucidation, Biomimetic Conversion, and Their Immunosuppressive Effects

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00574openalex-snapshot

Alpinoblonoids A and B, Two 16-nor-Labdane-Related Diterpenoids with a Tricyclic Carbon Skeleton from Alpinia oblongifolia

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00969openalex-snapshot

Asymmetric Allylboration of α-Alkoxy-enones: Access to Enantioenriched Tertiary α-Hydroxy Ketones

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01315openalex-snapshot

Euphorkanlide A, a Highly Modified Ingenane Diterpenoid with a C24 Appendage from Euphorbia kansuensis

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02630openalex-snapshot

Suadimins A–C, Unprecedented Dimeric Quinoline Alkaloids with Antimycobacterial Activity from Melodinus suaveolens

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

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

inferred← citeshttps://doi.org/10.1080/10286020.2019.1611787openalex-snapshot

Two new ent-abietane diterpenoids from Euphorbia helioscopia

inferred← citeshttps://doi.org/10.1080/14786419.2020.1719491openalex-snapshot

Euphanoids A and B, two new lathyrane diterpenoids with nitric oxide (NO) inhibitory activity from Euphorbia kansuensis

inferred← citeshttps://doi.org/10.1080/14786419.2020.1765342openalex-snapshot

Euphopanes A–C, three new diterpenoids from Euphorbia pekinensis

inferred← citeshttps://doi.org/10.15212/amm-2024-0050openalex-snapshot

Preliminary study on Zeqi: from pharmacological action of active ingredients to clinical application research

inferred← citeshttps://doi.org/10.3390/molecules26165055openalex-snapshot

Euphorbia Diterpenes: An Update of Isolation, Structure, Pharmacological Activities and Structure–Activity Relationship

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