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Cytotoxic Meroterpenoids with Rare Skeletons from Psidium guajava Cultivated in Temperate Zone

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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.201403082openalex-snapshot

Biomimetic Synthesis of (+)‐Ledene, (+)‐Viridiflorol, (−)‐Palustrol, (+)‐Spathulenol, and Psiguadial A, C, and D via the Platform Terpene (+)‐Bicyclogermacrene

inferredcites →https://doi.org/10.1002/chem.201500533openalex-snapshot

Guapsidial A and Guadials B and C: Three New Meroterpenoids with Unusual Skeletons from the Leaves of Psidium guajava

inferredcites →https://doi.org/10.1007/s13659-012-0102-4openalex-snapshot

Guajadials C-F, four unusual meroterpenoids from Psidium guajava

inferredcites →https://doi.org/10.1007/s13659-015-0066-2openalex-snapshot

Monoterpenoid Indole Alkaloids from Inadequately Dried Leaves of Alstonia scholaris

inferredcites →https://doi.org/10.1016/j.bmcl.2011.07.004openalex-snapshot

Yojironins E–I, prenylated acylphloroglucinols from Hypericum yojiroanum

inferredcites →https://doi.org/10.1016/j.fitote.2014.03.015openalex-snapshot

Flavonoids and stilbenoids from Derris eriocarpa

inferredcites →https://doi.org/10.1016/j.jep.2008.01.025openalex-snapshot

Psidium guajava: A review of its traditional uses, phytochemistry and pharmacology

inferredcites →https://doi.org/10.1016/j.tetlet.2011.04.106openalex-snapshot

Yojironins A−D, meroterpenoids and prenylated acylphloroglucinols from Hypericum yojiroanum

inferredcites →https://doi.org/10.1021/ja209809topenalex-snapshot

Two Separate Gene Clusters Encode the Biosynthetic Pathway for the Meroterpenoids Austinol and Dehydroaustinol in Aspergillus nidulans

inferredcites →https://doi.org/10.1021/np100489uopenalex-snapshot

Tuberatolides, Potent FXR Antagonists from the Korean Marine Tunicate Botryllus tuberatus

inferredcites →https://doi.org/10.1021/np300833yopenalex-snapshot

Antioxidant and Anti-inflammatory Meroterpenoids from the Brown Alga Cystoseira usneoides

inferredcites →https://doi.org/10.1021/np400359yopenalex-snapshot

Highly Oxygenated Meroterpenoids from Fruiting Bodies of the Mushroom Tricholoma terreum

inferredcites →https://doi.org/10.1021/ol2021548openalex-snapshot

Biyoulactones A–C, New Pentacyclic Meroterpenoids from Hypericum chinense

inferredcites →https://doi.org/10.1021/ol401991uopenalex-snapshot

Scopariusic Acid, a New Meroditerpenoid with a Unique Cyclobutane Ring Isolated from Isodon scoparius

inferredcites →https://doi.org/10.1021/ol503610bopenalex-snapshot

Applanatumin A, a New Dimeric Meroterpenoid from Ganoderma applanatum That Displays Potent Antifibrotic Activity

inferredcites →https://doi.org/10.1021/ol702537qopenalex-snapshot

Guajadial: An Unusual Meroterpenoid from Guava Leaves Psidium guajava

inferredcites →https://doi.org/10.1039/b820413fopenalex-snapshot

Meroterpenoids produced by fungi

inferredcites →https://doi.org/10.1039/c5np00027kopenalex-snapshot

Recent advances in the use of vibrational chiroptical spectroscopic methods for stereochemical characterization of natural products

inferredcites →https://doi.org/10.1039/c5np00090dopenalex-snapshot

Biosynthesis of fungal meroterpenoids

inferredcites →https://doi.org/10.1089/jmf.2011.1701openalex-snapshot

A Hexane Fraction of Guava Leaves ( Psidium guajava L.) Induces Anticancer Activity by Suppressing AKT/Mammalian Target of Rapamycin/Ribosomal p70 S6 Kinase in Human Prostate Cancer Cells

inferredcites →https://doi.org/10.3390/md13041726openalex-snapshot

Seco-Taondiol, an Unusual Meroterpenoid from the Chilean Seaweed Stypopodium flabelliforme and Its Gastroprotective Effect in Mouse Model

inferredcites →https://doi.org/10.3891/acta.chem.scand.22-3329openalex-snapshot

Phenol Dehydrogenations. 12. Oxidative Coupling of 3,5-Dimethyl-2,4,6-trihydroxybenzophenone.

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.2022.113551zenodo-depositor-declared

Cannabinoid-like meroterpenoids from Peperomia incana

inferred← citeshttps://doi.org/10.1002/ange.202506537openalex-snapshot

Enantioselective Total Synthesis of (–)‐Psiguadial A

inferred← citeshttps://doi.org/10.1002/anie.202506537openalex-snapshot

Enantioselective Total Synthesis of (–)‐Psiguadial A

inferred← citeshttps://doi.org/10.1002/cjoc.202000640openalex-snapshot

Guajamers A—I, Rearranged Polycyclic Phloroglucinol Meroterpenoids from Psidium guajava Leaves and Their Antibacterial Activity

inferred← citeshttps://doi.org/10.1007/s11101-020-09697-2openalex-snapshot

Phloroglucinols from Myrtaceae: attractive targets for structural characterization, biological properties and synthetic procedures

inferred← citeshttps://doi.org/10.1007/s13659-017-0138-6openalex-snapshot

Cytotoxic Acylphloroglucinol Derivatives from Callistemon salignus

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/b978-0-323-91294-5.00003-8openalex-snapshot

Bioactive hybrid compounds from Myrtaceae: Chemical classification and biological activities

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/j.bioorg.2020.103788openalex-snapshot

Polyphyllosides A–F, six new spirostanol saponins from the stems and leaves of Paris polyphylla var. chinensis

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.bmc.2025.118481openalex-snapshot

Synthesis of Psidium meroterpenoids with anti-hepatocellular carcinoma activities

inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.04.057openalex-snapshot

Cytotoxic steroidal saponins from Trillium kamtschaticum

inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105198openalex-snapshot

Meroterpenoids with unknown skeletons from the leaves of Psidium guajava including one anti-inflammatory and anticoagulant compound: psidial F

inferred← citeshttps://doi.org/10.1016/j.jep.2018.05.028openalex-snapshot

Seeing the light: Shifting from wild rhizomes to extraction of active ingredients from above-ground parts of Paris polyphylla var. yunnanensis

inferred← citeshttps://doi.org/10.1016/j.jfutfo.2022.12.005openalex-snapshot

A review of meroterpenoids and of their bioactivity from guava (Psidium guajava L.)

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.tet.2017.01.052openalex-snapshot

Acylphloroglucinol derivatives from the twigs and leaves of Callistemon salignus

inferred← citeshttps://doi.org/10.1016/j.tet.2017.05.096openalex-snapshot

Macathiohydantoins B–K, novel thiohydantoin derivatives from Lepidium meyenii

inferred← citeshttps://doi.org/10.1016/j.tet.2018.02.020openalex-snapshot

Formyl phloroglucinol meroterpenoids from Eucalyptus tereticornis and their bioactivities

inferred← citeshttps://doi.org/10.1016/j.tet.2018.09.050openalex-snapshot

Baeckfrutones A–L, polymethylated phloroglucinol meroterpenoids from the twigs and leaves of Baeckea frutescens

inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.03.038openalex-snapshot

Macahydantoins A and B, two new thiohydantoin derivatives from Maca (Lepidium meyenii): Structural elucidation and concise synthesis of macahydantoin A

inferred← citeshttps://doi.org/10.1016/j.tifs.2024.104822openalex-snapshot

A comprehensive review on guava: Nutritional profile, bioactive potential, and health-promoting properties of its pulp, peel, seeds, pomace and leaves

inferred← citeshttps://doi.org/10.1021/acs.jafc.7b01762openalex-snapshot

Meroterpenoids with Antitumor Activities from Guava (Psidium guajava)

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00139openalex-snapshot

NMR Fingerprints of Formyl Phloroglucinol Meroterpenoids and Their Application to the Investigation of Eucalyptus gittinsii subsp. gittinsii

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00443openalex-snapshot

Camaldulensals A–C, the First Meroterpenoids Possessing Two Spatially Separated Formyl Phloroglucinols Conjugated to a Terpene Core from the Leaves of Eucalyptus camaldulensis Dehnh

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.joc.8b00728openalex-snapshot

Evolution of a Strategy for the Enantioselective Total Synthesis of (+)-Psiguadial B

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02259openalex-snapshot

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

inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03299openalex-snapshot

Biomimetic Synthesis of Psiguajdianone Guided Discovery of the Meroterpenoids from Psidium guajava

inferred← citeshttps://doi.org/10.1038/s41598-017-01028-4openalex-snapshot

Psiguajadials A–K: Unusual Psidium Meroterpenoids as Phosphodiesterase-4 Inhibitors from the Leaves of Psidium guajava

inferred← citeshttps://doi.org/10.1039/c8ob01092gopenalex-snapshot

Biomimetic total syntheses of chromane meroterpenoids, guadials B and C, guapsidial A and psiguajadial D

inferred← citeshttps://doi.org/10.1039/d1ob00693bopenalex-snapshot

Psidguajones A and B, a pair of complex meroterpenoid epimers from the leaves of Psidium guajava

inferred← citeshttps://doi.org/10.1039/d5qo01496dopenalex-snapshot

Construction of the core skeleton for spiroaspertrione A by a Diels–Alder reaction of masked o -benzoquinone

inferred← citeshttps://doi.org/10.1080/10408398.2021.1945531openalex-snapshot

Guava (Psidium guajava L.): a glorious plant with cancer preventive and therapeutic potential

inferred← citeshttps://doi.org/10.1093/chromsci/bmz029openalex-snapshot

Eucalyptus Sideroxylon Bark Anti-inflammatory Potential, Its UPLC-PDA-ESI-qTOF-MS Profiling, and Isolation of a New Phloroglucinol

inferred← citeshttps://doi.org/10.2174/1386207326666230426093315openalex-snapshot

Psidium guajava: An Insight into Ethnomedicinal Uses, Phytochemistry, and Pharmacology

inferred← citeshttps://doi.org/10.31038/jppr.2020324openalex-snapshot

Cytotoxic Meroterpenes: A Review

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/biom11070957openalex-snapshot

Meroterpenoids: A Comprehensive Update Insight on Structural Diversity and Biology

inferred← citeshttps://doi.org/10.3390/metabo9030046openalex-snapshot

Ozone and Wounding Stresses Differently Alter the Temporal Variation in Formylated Phloroglucinols in Eucalyptus globulus Leaves

inferred← citeshttps://doi.org/10.3390/molecules27207016openalex-snapshot

Psidium guajava L. An Incalculable but Underexplored Food Crop: Its Phytochemistry, Ethnopharmacology, and Industrial Applications

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