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Isolation of Premyrsinane, Myrsinane, and Tigliane Diterpenoids from Euphorbia pithyusa Using a Chikungunya Virus Cell-Based Assay and Analogue Annotation by Molecular Networking

https://doi.org/10.1021/acs.jnatprod.7b00233
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What this work says

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

inferredcites →https://doi.org/10.1007/s11306-007-0082-2openalex-snapshot
Proposed minimum reporting standards for chemical analysis
inferredcites →https://doi.org/10.1016/0031-9422(94)00806-5openalex-snapshot
Four diterpene esters from Euphorbia myrsinites
inferredcites →https://doi.org/10.1016/0031-9422(95)00514-8openalex-snapshot
Diterpenes from euphorbia seguieriana
inferredcites →https://doi.org/10.1016/j.antiviral.2016.12.020openalex-snapshot
Protein kinases C as potential host targets for the inhibition of chikungunya virus replication
inferredcites →https://doi.org/10.1016/j.chroma.2015.09.092openalex-snapshot
Insights on profiling of phorbol, deoxyphorbol, ingenol and jatrophane diterpene esters by high performance liquid chromatography coupled to multiple stage mass spectrometry
inferredcites →https://doi.org/10.1016/j.drudis.2013.05.002openalex-snapshot
Chikungunya virus: an update on antiviral development and challenges
inferredcites →https://doi.org/10.1016/j.fitote.2014.05.015openalex-snapshot
Tigliane diterpenes from Croton mauritianus as inhibitors of chikungunya virus replication
inferredcites →https://doi.org/10.1016/j.fitote.2015.06.021openalex-snapshot
LC-MS2-Based dereplication of Euphorbia extracts with anti-Chikungunya virus activity
inferredcites →https://doi.org/10.1016/j.jaad.2010.12.038openalex-snapshot
Dual mechanism of action of ingenol mebutate gel for topical treatment of actinic keratoses: Rapid lesion necrosis followed by lesion-specific immune response
inferredcites →https://doi.org/10.1016/j.phytochem.2012.07.023openalex-snapshot
Antiviral chlorinated daphnane diterpenoid orthoesters from the bark and wood of Trigonostemon cherrieri
inferredcites →https://doi.org/10.1016/j.tet.2011.11.039openalex-snapshot
Cyclomyrsinane and premyrsinane diterpenes from Euphorbia falcata modulate resistance of cancer cells to doxorubicin
inferredcites →https://doi.org/10.1016/j.tips.2016.10.011openalex-snapshot
Molecular Networking As a Drug Discovery, Drug Metabolism, and Precision Medicine Strategy
inferredcites →https://doi.org/10.1016/j.vaccine.2012.08.025openalex-snapshot
US Military contributions to the global response to pandemic chikungunya
inferredcites →https://doi.org/10.1016/s0140-6736(11)60281-xopenalex-snapshot
Chikungunya: a re-emerging virus
inferredcites →https://doi.org/10.1016/s1473-3099(14)70948-xopenalex-snapshot
The Caribbean response to chikungunya
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00073openalex-snapshot
Antiviral Activity of Diterpene Esters on Chikungunya Virus and HIV Replication
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00116openalex-snapshot
Antiviral Activity of Flexibilane and Tigliane Diterpenoids from Stillingia lineata
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01016openalex-snapshot
Simplified Bryostatin Analogues Protect Cells from Chikungunya Virus-Induced Cell Death
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01017openalex-snapshot
Inhibition of Chikungunya Virus-Induced Cell Death by Salicylate-Derived Bryostatin Analogues Provides Additional Evidence for a PKC-Independent Pathway
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00260openalex-snapshot
Myrsinane, Premyrsinane, and Cyclomyrsinane Diterpenes from Euphorbia falcata as Potassium Ion Channel Inhibitors with Selective G Protein-Activated Inwardly Rectifying Ion Channel (GIRK) Blocking Effects
inferredcites →https://doi.org/10.1021/ci300563hopenalex-snapshot
ChemCalc: A Building Block for Tomorrow’s Chemical Infrastructure
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/jm400460dopenalex-snapshot
Chikungunya Virus: Emerging Targets and New Opportunities for Medicinal Chemistry
inferredcites →https://doi.org/10.1021/np200591hopenalex-snapshot
Bioactive Myrsinol Diterpenoids from the Roots of Euphorbia prolifera
inferredcites →https://doi.org/10.1021/np300637topenalex-snapshot
Prostratin and 12-O-Tetradecanoylphorbol 13-Acetate Are Potent and Selective Inhibitors of Chikungunya Virus Replication
inferredcites →https://doi.org/10.1021/np400413sopenalex-snapshot
Molecular Networking as a Dereplication Strategy
inferredcites →https://doi.org/10.1021/np500271uopenalex-snapshot
Jatrophane Diterpenes as Inhibitors of Chikungunya Virus Replication: Structure–Activity Relationship and Discovery of a Potent Lead
inferredcites →https://doi.org/10.1021/np990209uopenalex-snapshot
Diterpenoids from Euphorbia pithyusa subsp. cupanii
inferredcites →https://doi.org/10.1038/512124aopenalex-snapshot
US assesses virus of the Caribbean
inferredcites →https://doi.org/10.1038/nbt.3597openalex-snapshot
Sharing and community curation of mass spectrometry data with Global Natural Products Social Molecular Networking
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-0030-1264446openalex-snapshot
Pre-myrsinanes and deoxygenated phorboids from the Iranian spurge Euphorbia macroclada Boiss.
inferredcites →https://doi.org/10.1101/gr.1239303openalex-snapshot
Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks
inferredcites →https://doi.org/10.1111/1469-0691.12694openalex-snapshot
Globalization of Chikungunya: 10 years to invade the world
inferredcites →https://doi.org/10.1111/evo.12534openalex-snapshot
Evolutionary bursts in Euphorbia (Euphorbiaceae) are linked with photosynthetic pathway
inferredcites →https://doi.org/10.1111/j.1095-8339.1987.tb01036.xopenalex-snapshot
The saga of the spurges: a review of classification and relationships in the Euphorbiales
inferredcites →https://doi.org/10.2147/vdt.s25513openalex-snapshot
Current research and clinical trials for a vaccine against Chikungunya virus
inferredcites →https://doi.org/10.2807/1560-7917.es2014.19.41.20929openalex-snapshot
Concurrent outbreaks of dengue, chikungunya and Zika virus infections – an unprecedented epidemic wave of mosquito-borne viruses in the Pacific 2012–2014
inferredcites →https://doi.org/10.3390/molecules19033617openalex-snapshot
Trigocherrierin A, a Potent Inhibitor of Chikungunya Virus Replication
inferredcites →https://doi.org/10.5501/wjv.v1.i1.11openalex-snapshot
Emerging and re-emerging viruses: A global challenge illustrated by Chikungunya virus outbreaks
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.2019.112101zenodo-depositor-declared
Isolation of phenanthrenes and identification of phorbol ester derivatives as potential anti-CHIKV agents using FBMN and NAP from Sagotia racemosa
inferred← citeshttps://doi.org/10.1002/cbdv.202200918openalex-snapshot
Integration of LC/MS, NMR and Molecular Docking for Profiling of Bioactive Diterpenes from Euphorbia mauritanica L. with in Vitro Anti‐SARS‐CoV‐2 Activity
inferred← citeshttps://doi.org/10.1002/chir.70061openalex-snapshot
Anti‐Inflammatory Jatrophane Diterpenoids With Multiple Chiral Carbon Centers From Jatropha curcas
inferred← citeshttps://doi.org/10.1007/978-3-031-67180-7_1openalex-snapshot
Tigliane Diterpenoids
inferred← citeshttps://doi.org/10.1016/j.apsb.2024.04.031openalex-snapshot
Targeted isolation of antiviral cinnamoylphloroglucinol-terpene adducts from Cleistocalyx operculatus by building blocks-based molecular networking approach
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NO inhibitory diterpenoids as potential anti-inflammatory agents from Euphorbia antiquorum
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2019.01.004openalex-snapshot
Current status and contemporary approaches to the discovery of antitumor agents from higher plants
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Highly anticipated natural diterpenoids as an important source of new drugs in 2013–2023
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.2025.106525openalex-snapshot
Tigliane and premyrsinane diterpenoids from Euphorbia monostyla and their cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115458openalex-snapshot
Plants extracts from Cameroon pharmacopeia strongly inhibit the Chikungunya virus infection by targeting entry and replication steps
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.jpba.2025.116741openalex-snapshot
Molecular networking: An efficient tool for discovering and identifying natural products
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112360openalex-snapshot
Anti-HIV tigliane diterpenoids from Reutealis trisperma
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.115020openalex-snapshot
Diterpenoids from Euphorbia prolifera and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.115063openalex-snapshot
Discovery of myrsinane diterpenoids from Euphorbia monostyla with cytotoxic potential
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01363openalex-snapshot
Iron-Catalyzed Skeletal Conversion of Lathyrane to Premyrsinane Euphorbia Diterpenes and Their Cytotoxic Activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00087openalex-snapshot
Synthesis of Thioloformate-Containing Lathyrane Diterpene Derivates via a [3,3] Sigmatropic Rearrangement and Their Anti-HIV Activity
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Bioactivity-Based Molecular Networking for the Discovery of Drug Leads in Natural Product Bioassay-Guided Fractionation
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b01025openalex-snapshot
Structurally Diverse Diterpenoids from Sandwithia guyanensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00365openalex-snapshot
Phytotoxic ent-Isopimarane-Type Diterpenoids from Euphorbia hylonoma
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00800openalex-snapshot
Antiviral Compounds from Codiaeum peltatum Targeted by a Multi-informative Molecular Networks Approach
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00916openalex-snapshot
Investigation of Premyrsinane and Myrsinane Esters in Euphorbia cupanii and Euphobia pithyusa with MS2LDA and Combinatorial Molecular Network Annotation Propagation
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.orglett.8b01114openalex-snapshot
Pepluanols C–D, Two Diterpenoids with Two Skeletons from Euphorbia peplus
inferred← citeshttps://doi.org/10.1021/acsomega.6c04642openalex-snapshot
Isolation and Characterization of Unusual Terpene Derivatives from the Fungus Echinodontium tinctorium
inferred← citeshttps://doi.org/10.1021/jacsau.4c00889openalex-snapshot
A Systematic Approach to Discover New Natural Product Scaffolds Using Database-Derived Relative Mass Spectral Defects and Molecular Networking
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Studying Charge Migration Fragmentation of Sodiated Precursor Ions in Collision-Induced Dissociation at the Library Scale
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/10.1080/10286020.2020.1758931openalex-snapshot
Antimicrobial ent-abietane-type diterpenoids from the roots of Euphorbia wallichii
inferred← citeshttps://doi.org/10.1080/13543776.2020.1751817openalex-snapshot
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Bioprospecting of Soil-Derived Actinobacteria Along the Alar-Hotan Desert Highway in the Taklamakan Desert
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Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes
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Antimicrobial Diterpenes: Recent Development From Natural Sources
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Myrsinane-Type Diterpenes: A Comprehensive Review on Structural Diversity, Chemistry and Biological Activities
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Diterpenoids from Euphorbia gedrosiaca as Potential Anti-Proliferative Agents against Breast Cancer Cells
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Euphosantianane A–D: Antiproliferative Premyrsinane Diterpenoids from the Endemic Egyptian Plant Euphorbia Sanctae-Catharinae
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Euphosantianane E–G: Three New Premyrsinane Type Diterpenoids from Euphorbia sanctae-catharinae with Contribution to Chemotaxonomy
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Combination of Molecular Networking and LC-MS/MS Profiling in Investigating the Interrelationships between the Antioxidant and Antimicrobial Properties of Curculigo latifolia
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