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Hyperjapones A–E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum
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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/anie.200906678openalex-snapshot
Catalytic Asymmetric Total Synthesis of ent‐Hyperforin
inferredcites →https://doi.org/10.1002/anie.201103873openalex-snapshot
The Chemistry of the Polycyclic Polyprenylated Acylphloroglucinols
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/10.1016/s0031-9422(00)94784-8openalex-snapshot
Phloroglucinol derivatives from Hypericum japonicum
inferredcites →https://doi.org/10.1016/s0031-9422(99)00617-2openalex-snapshot
Phloroglucinol derivatives from Hypericum japonicum
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00057openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinol Congeners Possessing Diverse Structures from Hypericum henryi
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00721openalex-snapshot
Antibacterial Prenylated Acylphloroglucinols from Psorothamnus fremontii
inferredcites →https://doi.org/10.1021/acs.orglett.5b00100openalex-snapshot
Hypersubones A and B, New Polycyclic Acylphloroglucinols with Intriguing Adamantane Type Cores from Hypericum subsessile
inferredcites →https://doi.org/10.1021/acs.orglett.5b01419openalex-snapshot
Total Syntheses of (−)-Spirooliganones A and B and Their Diastereoisomers: Absolute Stereochemistry and Inhibitory Activity against Coxsackie Virus B3
inferredcites →https://doi.org/10.1021/cr0500582openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/ja312150dopenalex-snapshot
Enantioselective Total Synthesis of Hyperforin
inferredcites →https://doi.org/10.1021/ja5060302openalex-snapshot
Rapid Synthesis of Polyprenylated Acylphloroglucinol Analogs via Dearomative Conjunctive Allylic Annulation
inferredcites →https://doi.org/10.1021/np9004147openalex-snapshot
Cytotoxic Acylphloroglucinol Derivatives from the Twigs of Garcinia cowa
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/ol202181gopenalex-snapshot
Structural Reassignment of Cytosporolides A–C via Biomimetic Synthetic Studies and Reinterpretation of NMR Data
inferredcites →https://doi.org/10.1021/ol500808popenalex-snapshot
New Acylphloroglucinol Derivatives with Diverse Architectures from Hypericum henryi
inferredcites →https://doi.org/10.1021/ol502425fopenalex-snapshot
Hyperuralones A and B, New Acylphloroglucinol Derivatives with Intricately Caged Cores from Hypericum uralum
inferredcites →https://doi.org/10.1021/ol702537qopenalex-snapshot
Guajadial: An Unusual Meroterpenoid from Guava Leaves Psidium guajava
inferredcites →https://doi.org/10.1038/nchem.1170openalex-snapshot
The total synthesis of hyperpapuanone, hyperibone L, epi-clusianone and oblongifolin A
inferredcites →https://doi.org/10.1039/b600518gopenalex-snapshot
Phloroglucinol compounds of natural origin
inferredcites →https://doi.org/10.1039/c2cc32352dopenalex-snapshot
Hypercohin A, a new polycyclic polyprenylated acylphloroglucinol possessing an unusual bicyclo[5.3.1]hendecane core from Hypericum cohaerens
inferredcites →https://doi.org/10.1055/s-2006-960955openalex-snapshot
Sarothralin G: A New Antimicrobial Compound fromHypericum japonicum
inferredcites →https://doi.org/10.1055/s-2007-969154openalex-snapshot
Sarothralen A and B, New Antibiotic Compounds fromHypericum japonicum
inferredcites →https://doi.org/10.1080/10412905.2012.728082openalex-snapshot
Chemical composition of the aliphatic compounds rich essential oil ofHypericum japonicumThunb. ex Murray from India
inferredcites →https://doi.org/10.1107/s0021889807059870openalex-snapshot
Determination of absolute structure using Bayesian statistics on Bijvoet differences
inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot
On enantiomorph-polarity estimation
inferredcites →https://doi.org/10.5897/jmpr.9000010openalex-snapshot
A detailed chemical composition and antimicrobial activity of Hypericum richeri Vill. subsp. grisebachii (Boiss.) Nyman essential oil from Serbia
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.2019.112216zenodo-depositor-declared
Hyperelodiones A-C, monoterpenoid polyprenylated acylphoroglucinols from Hypericum elodeoides, induce cancer cells apoptosis by targeting RXRα
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112723zenodo-depositor-declared
Meroterpenoids from the leaves of Psidium guajava (guava) cultivated in Korea using MS/MS-based molecular networking
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113173zenodo-depositor-declared
Discovery of Undescribed Monoterpenoid Polyprenylated Acylphloroglucinols with Immunosuppressive Activities from Hypericum longistylum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113308zenodo-depositor-declared
Hyjapones A−D, trimethylated acyphloroglucinol meroterpenoids from Hypericum japonicum thunb. With anti-inflammatory activity
inferred← citeshttps://doi.org/10.2139/ssrn.4666804openalex-extracted
Inverse Electron Demand Diels-Alder Reaction in Total Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/ange.201606091openalex-snapshot
Biomimetic Total Synthesis of Hyperjapones A–E and Hyperjaponols A and C
inferred← citeshttps://doi.org/10.1002/anie.201606091openalex-snapshot
Biomimetic Total Synthesis of Hyperjapones A–E and Hyperjaponols A and C
inferred← citeshttps://doi.org/10.1002/cbdv.201800266openalex-snapshot
Antinociceptive Activity of Phloroglucinol Derivatives Isolated from Southern Brazilian Hypericum Species
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/chin.201633182openalex-snapshot
ChemInform Abstract: Hyperjapones A—E, Terpenoid Polymethylated Acylphloroglucinols from Hypericum japonicum.
inferred← citeshttps://doi.org/10.1002/cjoc.202200008openalex-snapshot
Undescribed Meroterpenoids from Hypericum japonicum with Neuroprotective Effects on H2O2 Insult SH‐SY5Y Cells Targeting Keap1‐Nrf2
inferred← citeshttps://doi.org/10.1002/pca.70053openalex-snapshot
Comprehensive Degradation Analysis of Swertiamarin: Stability‐Indicating Assay and Structure Elucidation of Degradation Products
inferred← citeshttps://doi.org/10.1007/978-3-030-52966-6_2openalex-snapshot
The Phytochemistry and Pharmacology of Hypericum
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_7openalex-snapshot
Classification of Diverse Novel Phloroglucinols
inferred← citeshttps://doi.org/10.1007/s11101-019-09646-8openalex-snapshot
Chemical synthesis of terpenoids with participation of cyclizations plus rearrangements of carbocations: a current overview
inferred← citeshttps://doi.org/10.1007/s12639-021-01410-0openalex-snapshot
In vitro study of the antioxidant, antiproliferative, and anthelmintic properties of some medicinal plants of Kokrajhar district, India
inferred← citeshttps://doi.org/10.1007/s13659-019-0206-1openalex-snapshot
Diverse Polyphenols from Hypericum faberi
inferred← citeshttps://doi.org/10.1007/s13659-022-00362-zopenalex-snapshot
Carascynol A, a hybrid of caryophyllane-type terpenoid and a C6 unit degraded by polyprenylated acylphloroglucinols from Hypericum ascyron
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
inferred← citeshttps://doi.org/10.1016/j.bioorg.2017.09.001openalex-snapshot
Polycyclic phloroglucinols as PTP1B inhibitors from Hypericum longistylum : Structures, PTP1B inhibitory activities, and interactions with PTP1B
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.03.025openalex-snapshot
Hyperpatulols A–I, spirocyclic acylphloroglucinol derivatives with anti-migration activities from the flowers of Hypericum patulum
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104275openalex-snapshot
Dimethylated acylphloroglucinol meroterpenoids with anti-oral-bacterial and anti-inflammatory activities from Hypericum elodeoides
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107354openalex-snapshot
Discovery of PXR agonists from Hypericum japonicum: A class of novel nonaromatic acylphloroglucinol-terpenoid adducts
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109292openalex-snapshot
Anti-neuroinflammatory polyprenylated acylphloroglucinols from Hypericum patulum: LC-MS/MS-guided isolation, semi-synthesis, and TLR4 inhibition
inferred← citeshttps://doi.org/10.1016/j.cplett.2020.138206openalex-snapshot
Physical mechanism and electric-magnetic interaction in ECD and ROA: Visualization methods on chirality
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.10.014openalex-snapshot
Chiral separation and absolute configurations of two pairs of racemic polyprenylated benzophenones from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104585openalex-snapshot
Triketone-terpene meroterpenoids from the leaves of Rhodomyrtus tomentosa
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104879openalex-snapshot
Sweritranslactone D, a hepatoprotective novel secoiridoid dimer with tetracyclic lactone skeleton from heat-transformed swertiamarin
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104984openalex-snapshot
Discovery of phloroglucinols from Hypericum japonicum as ferroptosis inhibitors
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.105985openalex-snapshot
(±)-hypermonanones A-G, seven pairs of monoterpenoid polyprenylated acylphloroglucinol enantiomers from Hypericum monanthemum
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106437openalex-snapshot
Hyperwightianols A–H, monoterpenoid demethylated acylphloroglucinol derivatives from Hypericum wightianum
inferred← citeshttps://doi.org/10.1016/j.jep.2026.122167openalex-snapshot
Hypericum japonicum Thunb. ex Murray inhibits hepatocellular carcinoma angiogenesis through the TF/FVIIa-mediated signaling pathway
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.08.002openalex-snapshot
Structural diversity and biological activities of phloroglucinol derivatives from Hypericum species
inferred← citeshttps://doi.org/10.1016/j.phytol.2026.104247openalex-snapshot
Chemical constituents from Hypericum japonicum and their PXR agonistic activity
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100066openalex-snapshot
Inverse electron demand Diels-Alder reaction in total synthesis of bioactive natural products
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/s1875-5364(18)30131-6openalex-snapshot
Advanced natural products chemistry research in China between 2015 and 2017
inferred← citeshttps://doi.org/10.1016/s1875-5364(24)60599-6openalex-snapshot
Hyparillums A and B: polycyclic polyprenylated acylphloroglucinols from Hypericum patulum
inferred← citeshttps://doi.org/10.1021/acs.accounts.1c00019openalex-snapshot
Biomimetic Dearomatization Strategies in the Total Synthesis of Meroterpenoid Natural Products
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00888openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols Bearing a Lavandulyl-Derived Substituent from Garcinia xanthochymus Fruits
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00131openalex-snapshot
Discovery of Dual-Target Anti-Alzheimer’s Filicinic Acid-Based Meroterpenoids from Hypericum japonicum Thunb.
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00606openalex-snapshot
Rearranged Phloroglucinol-Monoterpenoid Adducts from Callistemon rigidus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00017openalex-snapshot
Antibacterial Dimeric Acylphloroglucinols from Hypericum japonicum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01006openalex-snapshot
Prenylated Acylphloroglucinols from Hypericum faberi
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01077openalex-snapshot
The First Racemic Total Syntheses of the Antiplasmodials Watsonianones A and B and Corymbone B
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01720openalex-snapshot
Drychampones A–C: Three Meroterpenoids from Dryopteris championii
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02643openalex-snapshot
Frutescone A–G, Tasmanone-Based Meroterpenoids from the aerial parts of Baeckea frutescens
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02383openalex-snapshot
Sweritranslactones A–C: Unusual Skeleton Secoiridoid Dimers via [4 + 2] Cycloaddition from Swertiamarin
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01050openalex-snapshot
Phloroglucinol Derivatives with Unusual Skeletons from Cleistocalyx operculatus and Their in Vitro Antiviral Activity
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01817openalex-snapshot
Meroterpenoids with New Skeletons from Myrtus communis and Structure Revision of Myrtucommulone K
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02159openalex-snapshot
Biomimetic-Inspired Syntheses of Myrtucommuacetalone and Myrtucommulone J
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b04022openalex-snapshot
Norascyronones A and B, 2,3,4-nor-Polycyclic Polyprenylated Acylphloroglucinols from Hypericum ascyron
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00388openalex-snapshot
Garsubelone A, the First Dimeric Polycyclic Polyprenylated Acylphloroglucinols with Complicated Heptacyclic Architecture from Garcinia subelliptica
inferred← citeshttps://doi.org/10.1021/jacsau.5c00201openalex-snapshot
Total Synthesis of (−)-Elodeoidins A and B
inferred← citeshttps://doi.org/10.1038/s41570-022-00431-4openalex-snapshot
Demystifying racemic natural products in the homochiral world
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/c6cs00935bopenalex-snapshot
Recent applications of the 1,2-carbon atom migration strategy in complex natural product total synthesis
inferred← citeshttps://doi.org/10.1039/c6qo00620eopenalex-snapshot
Furanmonogones A and B: two rearranged acylphloroglucinols with a 4,5-seco-3(2H)-furanone core from the flowers of Hypericum monogynum
inferred← citeshttps://doi.org/10.1039/c7ra05947gopenalex-snapshot
Norsampsone E, an unprecedented decarbonyl polycyclic polyprenylated acylphloroglucinol with a homoadamantyl core from Hypericum sampsonii
inferred← citeshttps://doi.org/10.1039/c8ob02433bopenalex-snapshot
Atropisomeric meroterpenoids with rare triketone-phloroglucinol-terpene hybrids from Baeckea frutescens
inferred← citeshttps://doi.org/10.1039/c9np00037bopenalex-snapshot
Naturally occurring [4 + 2] type terpenoid dimers: sources, bioactivities and total syntheses
inferred← citeshttps://doi.org/10.1039/c9qo00245fopenalex-snapshot
The absolute configurations of hyperilongenols A–C: rare 12,13- seco -spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
inferred← citeshttps://doi.org/10.1039/c9qo90045dopenalex-snapshot
Correction: The absolute configurations of hyperilongenols A–C: rare 12,13- seco -spirocyclic polycyclic polyprenylated acylphloroglucinols with enolizable β,β′-tricarbonyl systems from Hypericum longistylum Oliv.
inferred← citeshttps://doi.org/10.1039/d0qo01118eopenalex-snapshot
Elodeoidins A–H, acylphloroglucinol meroterpenoids possessing diverse rearranged skeletons from Hypericum elodeoides
inferred← citeshttps://doi.org/10.1039/d1np00077bopenalex-snapshot
Recent advances in the synthesis of natural products containing the phloroglucinol motif
inferred← citeshttps://doi.org/10.1039/d1qo00989copenalex-snapshot
A biomimetic synthesis-enabled stereochemical assignment of rhodotomentones A and B, two unusual caryophyllene-derived meroterpenoids from Rhodomyrtus tomentosa
inferred← citeshttps://doi.org/10.1039/d2ob00370hopenalex-snapshot
Cephaloliverols A and B, two sterol-hybrid meroterpenoids from Cephalotaxus oliveri
inferred← citeshttps://doi.org/10.1039/d2ob01851aopenalex-snapshot
Hyperpatone A, a polycyclic polyprenylated acylphloroglucinol with a rare 8/6/5/6/5 pentacyclic skeleton from Hypericum patulum
inferred← citeshttps://doi.org/10.1039/d3qo00835eopenalex-snapshot
Patriniaterpenes A–D: unveiling the unique structure and antioxidant properties of monoterpene–sesquiterpene conjugates from Patrinia scabra
inferred← citeshttps://doi.org/10.1071/ch18141openalex-snapshot
Biomimetic Synthesis of Hyperjapones F-I
inferred← citeshttps://doi.org/10.1080/10286020.2017.1391229openalex-snapshot
Survey of natural products reported by Asian research groups in 2016
inferred← citeshttps://doi.org/10.3390/biomedicines9101473openalex-snapshot
Unprecedented Monoterpenoid Polyprenylated Acylphloroglucinols with a Rare 6/6/5/4 Tetracyclic Core, Enhanced MCF-7 Cells’ Sensitivity to Camptothecin by Inhibiting the DNA Damage Response
inferred← citeshttps://doi.org/10.3390/ph15111392openalex-snapshot
Total Synthesis of Terpenes and Their Biological Significance: A Critical Review
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