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Biyoulactones A–C, New Pentacyclic Meroterpenoids from Hypericum chinense
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.tetlet.2009.06.021openalex-snapshot
Yezo’otogirins A–C, new tricyclic terpenoids from Hypericum yezoense
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/np8001145openalex-snapshot
Phloroglucinols with Antioxidant Activity and Xanthonolignoids from the Heartwood of Hypericum geminiflorum
inferredcites →https://doi.org/10.1021/ol050960wopenalex-snapshot
Biyouyanagin A, an Anti-HIV Agent from Hypericum chinense L. var. salicifolium
inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot
On enantiomorph-polarity estimation
inferredcites →https://doi.org/10.1246/cl.1987.1337openalex-snapshot
Antimicrobial Compounds, Chinesin I and II from Flowers of Hypericum chinense L.
inferredcites →https://doi.org/10.3987/com-09-s(s)28openalex-snapshot
Biyouxanthones A - D, Prenylated Xanthones from Roots of Hypericum chinense
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.2021.112970zenodo-depositor-declared
Chemical constituents from the flowers of Hypericum monogynum L. with COX-2 inhibitory activity
inferred← citeshttps://doi.org/10.1002/ajoc.201500360openalex-snapshot
Involudispirones A and B: Sesterterpenes Containing a Dispiro Ring from Stahlianthus involucratus
inferred← citeshttps://doi.org/10.1002/ange.202016178openalex-snapshot
Total Synthesis of the Meroterpenoid Manginoid A as Fueled by a Challenging Pinacol Coupling and Bicycle‐forming Etherification
inferred← citeshttps://doi.org/10.1002/ange.202203311openalex-snapshot
Intramolecular Tricarbonyl‐Ene Reactions and α‐Hydroxy‐β‐Diketone Rearrangements Inspired by the Biosynthesis of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1002/anie.202016178openalex-snapshot
Total Synthesis of the Meroterpenoid Manginoid A as Fueled by a Challenging Pinacol Coupling and Bicycle‐forming Etherification
inferred← citeshttps://doi.org/10.1002/anie.202203311openalex-snapshot
Intramolecular Tricarbonyl‐Ene Reactions and α‐Hydroxy‐β‐Diketone Rearrangements Inspired by the Biosynthesis of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1002/cbdv.201300304openalex-snapshot
Recent Advances Regarding Constituents and Bioactivities of Plants from the GenusHypericum
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/mco2.70960openalex-snapshot
SPR‐UPLC‐QTOF/MS‐GNPS‐Guided Discovery of Hypermonol J as a Novel Tumor Necrosis Factor‐Binding Small‐Molecule Lead for Inflammatory Storm Intervention
inferred← citeshttps://doi.org/10.1002/slct.202504003openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols (PPAPs) Kouytchin A‐B and a Tetramethoxydibenzo[1,4]Dioxin From Hypericum kouytchense : Isolation and Cytotoxic Evaluation
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/s10600-015-1429-yopenalex-snapshot
Two New Flavones from Hypericum chinense and Their Anti-Tobacco Mosaic Virus Activity
inferred← citeshttps://doi.org/10.1007/s11418-014-0853-9openalex-snapshot
Hypelodins A and B, polyprenylated benzophenones from Hypericum elodeoides
inferred← citeshttps://doi.org/10.1007/s11418-021-01489-yopenalex-snapshot
Characteristic metabolites of Hypericum plants: their chemical structures and biological activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.03.001openalex-snapshot
Hikiokoshins A–I, diterpenes from the leaves of Isodon japonicus
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113727openalex-snapshot
Structurally diverse spirocyclic polycyclic polyprenylated acylphloroglucinols from Hypericum ascyron Linn. and their anti-tumor activity
inferred← citeshttps://doi.org/10.1016/j.tet.2016.08.064openalex-snapshot
Cadinane-type sesquiterpenoids from Stahlianthus involucratus and their absolute configurations
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130784openalex-snapshot
Novel rearranged acetophenone derivatives possessing diverse architectures from the leaves of Melicope ptelefolia
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.01.052openalex-snapshot
Biyoulactones D and E, meroterpenoids from Hypericum chinense
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.02.089openalex-snapshot
Frondhyperins A–D, short ketide–phenylketide conjugates from Hypericum frondosum cv. Sunburst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.09.071openalex-snapshot
Spirocyclic polycyclic polyprenylated acylphloroglucinols from the ethyl acetate fraction of Hypericum henryi
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151220openalex-snapshot
Hyphenone A, the first 3,3-diisoprenylated bicyclic polyprenylated acylphloroglucinols as Cav3.1 T-type calcium channel inhibitor from Hypericum henryi
inferred← citeshttps://doi.org/10.1016/s1875-5364(25)60911-3openalex-snapshot
Naturally occurring seco- and nor-polycyclic polyprenylated acylphloroglucinols: distribution, structural diversity, andbiological activity
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00551openalex-snapshot
Research Progress of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00680openalex-snapshot
Cytotoxic Components from Hypericum elodeoides Targeting RXRα and Inducing HeLa Cell Apoptosis through Caspase-8 Activation and PARP Cleavage
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00354openalex-snapshot
Hypascyrins A–E, Prenylated Acylphloroglucinols from Hypericum ascyron
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00811openalex-snapshot
Hymoins A–D: Two Pairs of Polyprenylated Acylphloroglucinols from Hypericum monogynum and Their Light-Induced Transformation
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02725openalex-snapshot
Hypatulins A and B, Meroterpenes from Hypericum patulum
inferred← citeshttps://doi.org/10.1021/np500827hopenalex-snapshot
Prenylated Benzophenones from Triadenum japonicum
inferred← citeshttps://doi.org/10.1038/s41598-020-79305-yopenalex-snapshot
Unusual derivatives from Hypericum scabrum
inferred← citeshttps://doi.org/10.1038/srep29744openalex-snapshot
Involucratusins A–H: Unusual Cadinane Dimers from Stahlianthus involucratus with Multidrug Resistance Reversal Activity
inferred← citeshttps://doi.org/10.1038/srep32748openalex-snapshot
Cytotoxic Meroterpenoids with Rare Skeletons from Psidium guajava Cultivated in Temperate Zone
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/c9qo01365bopenalex-snapshot
Phomeroids A and B: two novel cytotoxic meroterpenoids from the deep-sea-derived fungus Phomopsis tersa FS441
inferred← citeshttps://doi.org/10.1039/d1qo01302eopenalex-snapshot
Hyperbeanone A, a 5,6- seco -spirocyclic polycyclic polyprenylated acylphloroglucinol derivative with an unprecedented skeleton from Hypericum beanii
inferred← citeshttps://doi.org/10.1039/d5ob00045aopenalex-snapshot
A synthetic investigation into the biosynthesis of hypsampsone A
inferred← citeshttps://doi.org/10.1248/cpb.c16-00243openalex-snapshot
Yezo’otogirins D–H, Acylphloroglucinols and Meroterpenes from Hypericum yezoense
inferred← citeshttps://doi.org/10.1248/yakushi.15-00198openalex-snapshot
Search for Structurally Unique Bioactive Natural Products
inferred← citeshttps://doi.org/10.3762/bjoc.11.29openalex-snapshot
Synthesis of the furo[2,3-b]chromene ring system of hyperaspindols A and B
inferred← citeshttps://doi.org/10.3987/com-13-12842openalex-snapshot
Cytotoxic Xanthones from Hypericum chinense
inferred← citeshttps://doi.org/10.3987/rev-14-sr(k)1openalex-snapshot
Prenylated Acylphloroglucinols and Meroterpenoids from Hypericum Plants
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