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Eucalyptusdimers A–C, Dimeric Phloroglucinol–Phellandrene Meroterpenoids from Eucalyptus robusta

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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/chem.201601732openalex-snapshot
1H NMR‐Guided Isolation of Formyl‐Phloroglucinol Meroterpenoids from the Leaves of Eucalyptus robusta
inferredcites →https://doi.org/10.1007/s13659-011-0021-9openalex-snapshot
Euglobal-IIIa, a novel acylphloroglucinol-sesquiterpene derivative from Eucalyptus robusta: absolute structure and cytotoxicity
inferredcites →https://doi.org/10.1007/s13659-017-0138-6openalex-snapshot
Cytotoxic Acylphloroglucinol Derivatives from Callistemon salignus
inferredcites →https://doi.org/10.1016/j.tet.2017.01.052openalex-snapshot
Acylphloroglucinol derivatives from the twigs and leaves of Callistemon salignus
inferredcites →https://doi.org/10.1016/s0031-9422(97)00672-9openalex-snapshot
Phloroglucinol-monoterpene adducts from Eucalyptus grandis
inferredcites →https://doi.org/10.1016/s0031-9422(98)00289-1openalex-snapshot
Five phloroglucinol-monoterpene adducts from Eucalyptus grandis
inferredcites →https://doi.org/10.1021/acs.jafc.7b01762openalex-snapshot
Meroterpenoids with Antitumor Activities from Guava (Psidium guajava)
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00090openalex-snapshot
Eucarobustols A–I, Conjugates of Sesquiterpenoids and Acylphloroglucinols from Eucalyptus robusta
inferredcites →https://doi.org/10.1021/acs.orglett.5b03117openalex-snapshot
Guajavadimer A, a Dimeric Caryophyllene-Derived Meroterpenoid with a New Carbon Skeleton from the Leaves of Psidium guajava
inferredcites →https://doi.org/10.1021/acs.orglett.8b00238openalex-snapshot
Biomimetic Syntheses of Callistrilones A–E via an Oxidative [3 + 2] Cycloaddition
inferredcites →https://doi.org/10.1021/jm3007454openalex-snapshot
Potent HGF/c-Met Axis Inhibitors from Eucalyptus globulus: the Coupling of Phloroglucinol and Sesquiterpenoid Is Essential for the Activity
inferredcites →https://doi.org/10.1021/np9604994openalex-snapshot
Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus
inferredcites →https://doi.org/10.1021/np990056aopenalex-snapshot
New Insecticidal Tetradecahydroxanthenediones from Callistemon viminalis
inferredcites →https://doi.org/10.1021/np9900573openalex-snapshot
A New Insecticidal Pyranocyclohexenedione from Kunzea ericifolia
inferredcites →https://doi.org/10.1021/ol100138kopenalex-snapshot
A Short Biomimetic Synthesis of the Meroterpenoids Guajadial and Psidial A
inferredcites →https://doi.org/10.1021/ol7025075openalex-snapshot
Eucalyptals A−C with a New Skeleton Isolated from Eucalyptus globulus
inferredcites →https://doi.org/10.1038/srep32748openalex-snapshot
Cytotoxic Meroterpenoids with Rare Skeletons from Psidium guajava Cultivated in Temperate Zone
inferredcites →https://doi.org/10.1038/srep39815openalex-snapshot
New Formyl Phloroglucinol Meroterpenoids from the Leaves of Eucalyptus robusta
inferredcites →https://doi.org/10.1039/b600518gopenalex-snapshot
Phloroglucinol compounds of natural origin
inferredcites →https://doi.org/10.1039/c4ra01078gopenalex-snapshot
Eucalmaidials A and B, phloroglucinol-coupled sesquiterpenoids from the juvenile leaves of Eucalyptus maideni

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.2022.113565zenodo-depositor-declared
Acylphloroglucinol-monoterpene meroterpenoids from Eucalyptus tereticornis and their inhibitory activity against ATP citrate lyase
inferred← citeshttps://doi.org/10.1002/ange.201814421openalex-snapshot
Isolation and Synthesis of Novel Meroterpenoids from Rhodomyrtus tomentosa: Investigation of a Reactive Enetrione Intermediate
inferred← citeshttps://doi.org/10.1002/anie.201814421openalex-snapshot
Isolation and Synthesis of Novel Meroterpenoids from Rhodomyrtus tomentosa: Investigation of a Reactive Enetrione Intermediate
inferred← citeshttps://doi.org/10.1002/cbdv.202000489openalex-snapshot
Polymethylated Phloroglucinol Meroterpenoids from Rhodomyrtus tomentosa and Their Antibacterial and Acetylcholinesterase Inhibitory Effects
inferred← citeshttps://doi.org/10.1002/cbdv.202200025openalex-snapshot
Structural Diversity of Complex Phloroglucinol Derivatives from Eucalyptus Species
inferred← citeshttps://doi.org/10.1002/cbdv.202500312openalex-snapshot
New Phenolic Compounds from Eucalyptus tereticornis with Antioxidant Activity
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_14openalex-snapshot
Biological Activities
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_7openalex-snapshot
Classification of Diverse Novel Phloroglucinols
inferred← citeshttps://doi.org/10.1007/s13659-018-0189-3openalex-snapshot
Structurally Diverse Polymethylated Phloroglucinol Meroterpenoids from Baeckea frutescens
inferred← citeshttps://doi.org/10.1016/b978-0-12-816455-6.00014-7openalex-snapshot
Analysis of meroterpenoids
inferred← citeshttps://doi.org/10.1016/b978-0-323-95047-3.00005-8openalex-snapshot
Terpenes, meroterpenoids, and artemisinin and SARS-CoV-2
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.08.022openalex-snapshot
Ethnopharmacology, phytochemistry and pharmacology of potent antibacterial medicinal plants from Africa
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104127openalex-snapshot
Acylphloroglucinols with acetylcholinesterase inhibitory effects from the fruits of Eucalyptus robusta
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104519openalex-snapshot
Polymethylated acylphloroglucinols from Rhodomyrtus tomentosa exert acetylcholinesterase inhibitory effects
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105404openalex-snapshot
Acylphloroglucinol trimers from Callistemon salignus seeds: Isolation, configurational assignment, hAChE inhibitory effects, and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106159openalex-snapshot
Eucarbwenstols A–H, eight novel compounds from Eucalyptus robusta prevents MPC-5 injury via ROS modulation and regulation of mitochondrial membrane potential
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106836openalex-snapshot
Oligomeric phloroglucinols with hAChE inhibitory and antibacterial activities from tropic Rhodomyrtus tomentosa
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109468openalex-snapshot
Rubiginoids A–N, phytocannabinoid-like meroterpenoids with diverse ring systems from Rhododendron rubiginosum
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.109681openalex-snapshot
New bis-β-triketone-sesquiterpene adducts from Corymbia citriodora with lysosomal biogenesis-inducing activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104418openalex-snapshot
Tyrosinase inhibitors from the leaves of Eucalyptus globulus
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140388openalex-snapshot
Isolation, characterization, and anti-MRSA activity of formyl-phloroglucinol-derivatives from Eucalyptus robusta fruits
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.04.008openalex-snapshot
Twelve formyl phloroglucinol meroterpenoids from the leaves of Eucalyptus robusta
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113179openalex-snapshot
Phloroglucinol–meroterpenoids from the leaves of Eucalyptus camaldulensis Dehnh.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113394openalex-snapshot
Phloroglucinols with hAChE and α-glucosidase inhibitory activities from the leaves of tropic Rhodomyrtus tomentosa
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114241openalex-snapshot
Phytocannabinoid-like meroterpenoids from twigs and leaves of Rhododendron spinuliferum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114254openalex-snapshot
Acetylcholinesterase inhibitory phloroglucinols from tropic Rhodomyrtus tomentosa
inferred← citeshttps://doi.org/10.1016/j.surfin.2022.102545openalex-snapshot
Sustainable synthesis of silver nanoparticles with enhanced anticancer, antibacterial, and antioxidant properties mediated by dimeric 2,4-diacetyl phloroglucinol: Experimental and computational insights
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151872openalex-snapshot
Artemilavanolides A and B, two sesquiterpenoids with a 6-oxabicyclo[3.2.1]octane scaffold from Artemisia lavandulaefolia
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c00828openalex-snapshot
New Monoterpene Acid and Gallic Acid Glucose Esters with Anti-Inflammatory Activity from Blue Gum ( Eucalyptus globulus ) Leaves
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c13084openalex-snapshot
Chemical Profiles and Biological Effects of Polyphenols in Eucalyptus Genus: A Comprehensive Review on Their Applications in Human Health and the Food Industry
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00430openalex-snapshot
Eucalypglobulusals A–J, Formyl-Phloroglucinol–Terpene Meroterpenoids from Eucalyptus globulus Fruits
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00109openalex-snapshot
Leptosperols A and B, Two Cinnamoylphloroglucinol–Sesquiterpenoid Hybrids from Leptospermum scoparium : Structural Elucidation and Biomimetic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02170openalex-snapshot
Novel Meroterpenoids from Hypericum patulum: Highly Potent Late Nav1.5 Sodium Current Inhibitors
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02522openalex-snapshot
Total Synthesis of Guajavadimer A via Lewis Acid-Catalyzed Cascade Double Hetero-Diels–Alder Reactions
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01175openalex-snapshot
Total Synthesis of Eucalyptusdimers A–C
inferred← citeshttps://doi.org/10.1039/c8np90032aopenalex-snapshot
Hot off the Press
inferred← citeshttps://doi.org/10.1039/c8qo01379aopenalex-snapshot
Fischernolides A–D, four novel diterpene-based meroterpenoid scaffolds with antitumor activities from Euphorbia fischeriana
inferred← citeshttps://doi.org/10.1039/d0nj06114jopenalex-snapshot
Toward an efficient and eco-friendly route for the synthesis of dimeric 2,4-diacetyl phloroglucinol and its potential as a SARS-CoV-2 main protease antagonist: insight from in silico studies
inferred← citeshttps://doi.org/10.1080/14786419.2022.2118742openalex-snapshot
New acylphloroglucinols from a crude acetone extract of Eucalyptus camaldulensis Dehnh. leaf
inferred← citeshttps://doi.org/10.1080/14786419.2023.2244132openalex-snapshot
Phytochemical characterization and antifungal potential of leaf extracts of Mosiera bullata
inferred← citeshttps://doi.org/10.1080/87559129.2021.1877300openalex-snapshot
New Insights into the Biological Properties of Eucalyptus-Derived Essential Oil: A Promising Green Anti-Cancer Drug
inferred← citeshttps://doi.org/10.2139/ssrn.4848548openalex-snapshot
Discovery of Structurally Intriguing Hache Inhibitors from Tropic Rhodomyrtus Tomentosa Leaves: Isolation, Configuration Assignment, Hache Inhibitory Activities, and Molecular Docking Studies
inferred← citeshttps://doi.org/10.3389/fphar.2022.830103openalex-snapshot
Biological activities of meroterpenoids isolated from different sources
inferred← citeshttps://doi.org/10.3389/fpls.2019.00186openalex-snapshot
Quantification and Localization of Formylated Phloroglucinol Compounds (FPCs) in Eucalyptus Species
inferred← citeshttps://doi.org/10.3390/antibiotics10070761openalex-snapshot
HPLC-PDA-ESI-MS/MS Profiling and Anti-Biofilm Potential of Eucalyptussideroxylon Flowers
inferred← citeshttps://doi.org/10.3390/biom11070957openalex-snapshot
Meroterpenoids: A Comprehensive Update Insight on Structural Diversity and Biology
inferred← citeshttps://doi.org/10.3390/molecules26123563openalex-snapshot
Interaction of Natural Compounds in Licorice and Turmeric with HIV-NCp7 Zinc Finger Domain: Potential Relevance to the Mechanism of Antiviral Activity
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