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Guajavadimer A, a Dimeric Caryophyllene-Derived Meroterpenoid with a New Carbon Skeleton from the Leaves of Psidium guajava

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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/s11010-011-0876-4openalex-snapshot
PTP1B inhibitor improves both insulin resistance and lipid abnormalities in vivo and in vitro
inferredcites →https://doi.org/10.1007/s13659-012-0102-4openalex-snapshot
Guajadials C-F, four unusual meroterpenoids from Psidium guajava
inferredcites →https://doi.org/10.1016/j.jep.2008.01.025openalex-snapshot
Psidium guajava: A review of its traditional uses, phytochemistry and pharmacology
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C-Methyl-flavonoids from the leaf waxes of some Myrtaceae
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Bioactive Sesquiterpenoids from the Rhizomes of Acorus calamus
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A Short Biomimetic Synthesis of the Meroterpenoids Guajadial and Psidial A
inferredcites →https://doi.org/10.1021/ol101062fopenalex-snapshot
Cytosporolides A−C, Antimicrobial Meroterpenoids with a Unique Peroxylactone Skeleton from Cytospora sp.
inferredcites →https://doi.org/10.1021/ol102179uopenalex-snapshot
Psiguadials A and B, Two Novel Meroterpenoids with Unusual Skeletons from the Leaves of Psidium guajava
inferredcites →https://doi.org/10.1021/ol203498aopenalex-snapshot
Physangulidines A, B, and C: Three New Antiproliferative Withanolides from Physalis angulata L.
inferredcites →https://doi.org/10.1021/ol302423bopenalex-snapshot
Guadial A and Psiguadials C and D, Three Unusual Meroterpenoids from Psidium guajava
inferredcites →https://doi.org/10.1021/ol302849vopenalex-snapshot
Isolation and Biomimetic Synthesis of (±)-Guajadial B, a Novel Meroterpenoid from Psidium guajava
inferredcites →https://doi.org/10.1021/ol303168yopenalex-snapshot
Kadcoccitones A and B, Two New 6/6/5/5-Fused Tetracyclic Triterpenoids from Kadsura coccinea
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Eucalyptals A−C with a New Skeleton Isolated from Eucalyptus globulus
inferredcites →https://doi.org/10.1021/ol702537qopenalex-snapshot
Guajadial: An Unusual Meroterpenoid from Guava Leaves Psidium guajava
inferredcites →https://doi.org/10.1021/ol9024869openalex-snapshot
Psidials A−C, Three Unusual Meroterpenoids from the Leaves of Psidium guajava L
inferredcites →https://doi.org/10.1248/cpb.30.1952openalex-snapshot
The granulation-inhibiting principles from Eucalyptus globulus Labill. II. The structures of euglobal-Ia1,-Ia2,-Ib,-Ic,-IIa,IIb and -IIc.
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The granulation-inhibiting principles from Eucalyptus globulus Labill. III. The structures of euglobal-III,-IVb and -VII.
inferredcites →https://doi.org/10.1248/cpb.41.1790openalex-snapshot
2'-Hydroxymatteucinol, a New C-Methyl Flavanone Derivative from Matteccia orientalis; Potent Hypoglycemic Activity in Streptozotocin (STZ)-Induced Diabetic Rat.

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.2021.112746zenodo-depositor-declared
Chemical constituents of Psidium guajava leaves and their antibacterial activity
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/cjoc.202000640openalex-snapshot
Guajamers A—I, Rearranged Polycyclic Phloroglucinol Meroterpenoids from Psidium guajava Leaves and Their Antibacterial Activity
inferred← citeshttps://doi.org/10.1002/slct.73877openalex-snapshot
Chemistry of Natural Terpenoids Caryophyllene and Caryophyllene Oxide: A Review of Recent Advances
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_7openalex-snapshot
Classification of Diverse Novel Phloroglucinols
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inferred← citeshttps://doi.org/10.1007/s11101-020-09698-1openalex-snapshot
Natural disesquiterpenoids: an overview of their chemical structures, pharmacological activities, and biosynthetic pathways
inferred← citeshttps://doi.org/10.1016/b978-0-323-91294-5.00003-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105277openalex-snapshot
Dibenzocyclooctadiene lignans from Kadsura coccinea alleviate APAP-induced hepatotoxicity via oxidative stress inhibition and activating the Nrf2 pathway in vitro
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Hepatoprotective compounds from fruits of (Lem.) A. C. Smith (Schisandraceae) and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.cclet.2020.11.028openalex-snapshot
Psiguamers A–C, three cytotoxic meroterpenoids bearing a methylated benzoylphloroglucinol framework from Psidium guajava and total synthesis of 1 and 2
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.foodres.2017.12.042openalex-snapshot
UPLC/QTOF/MS profiling of two Psidium species and the in-vivo hepatoprotective activity of their nano-formulated liposomes
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.phytochem.2021.112678openalex-snapshot
Heilaohuguosus A-S from the fruits of Kadsura coccinea and their hepatoprotective activity
inferred← citeshttps://doi.org/10.1016/j.phytol.2026.104172openalex-snapshot
Hepatoprotective and anti-inflammatory dibenzocyclooctadiene lignans from fruits of Kadsura coccinea
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135101openalex-snapshot
Diels-Alder reaction: A versatile synthetic tool for the synthesis of terpenoids and alkaloids: A review
inferred← citeshttps://doi.org/10.1016/j.tet.2026.135477openalex-snapshot
Recent developments in phloroglucinol and avarane meroterpenoid natural product total synthesis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.058openalex-snapshot
Hyperjapones F–I, terpenoid polymethylated acylphloroglucinols from Hypericum japonicum
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.03.059openalex-snapshot
Biomimetic total synthesis and structure confirmation of myrtucommulone K
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154575openalex-snapshot
Psidials L and M and Psipinene, three novel meroterpenoids with significant protective activity toward cisplatin-damaged HK2 cells from the leaves of Psidium guajava
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/10.1016/s1875-5364(18)30131-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jafc.0c07125openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jafc.7b01762openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jafc.9b04318openalex-snapshot
New Acylated Phenolic Glycosides with ROS-Scavenging Activity from Psidium guajava Leaves
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.4c01099openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00934openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.8b01050openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02522openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04234openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01817openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01175openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03815openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.9b06592openalex-snapshot
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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/c6np90012gopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c8qo01379aopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c9np00062copenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c9qo00174copenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d1ob00693bopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d1qo00989copenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d1qo01056eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d4ob01936aopenalex-snapshot
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Survey of natural products reported by Asian research groups in 2016
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Four meroterpenoids from the leaves of Psidium guajava L. and their cytotoxicity activities
inferred← citeshttps://doi.org/10.2174/1386207326666230426093315openalex-snapshot
Psidium guajava: An Insight into Ethnomedicinal Uses, Phytochemistry, and Pharmacology
inferred← citeshttps://doi.org/10.3389/fchem.2018.00045openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biom11070957openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms19123776openalex-snapshot
Therapeutic Potential of Plants and Plant Derived Phytochemicals against Acetaminophen-Induced Liver Injury
inferred← citeshttps://doi.org/10.3390/molecules22010065openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules25020260openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules27207016openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants9111582openalex-snapshot
Progress in the Chemistry of Macrocyclic Meroterpenoids
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