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Prenylated Acylphloroglucinols, Chipericumins A–D, from Hypericum chinense

https://doi.org/10.1021/np200741x

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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.bmc.2008.03.076openalex-snapshot

Petiolins A–C, phloroglucinol derivatives from Hypericum pseudopetiolatum var. kiusianum

inferredcites →https://doi.org/10.1016/j.bmcl.2010.06.047openalex-snapshot

Petiolins J–M, prenylated acylphloroglucinols from Hypericum pseudopetiolatum var. kiusianum

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.phytochem.2008.04.026openalex-snapshot

Tomoeones A–H, cytotoxic phloroglucinol derivatives from Hypericum ascyron

inferredcites →https://doi.org/10.1016/j.tet.2008.11.068openalex-snapshot

Harrisotones A–E, five novel prenylated polyketides with a rare spirocyclic skeleton from Harrisonia perforata

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/cr0500582openalex-snapshot

Polycyclic Polyprenylated Acylphloroglucinols

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/np900109yopenalex-snapshot

Acylphloroglucinol, Biyouyanagiol, Biyouyanagin B, and Related Spiro-lactones from Hypericum chinense

inferredcites →https://doi.org/10.1039/b600518gopenalex-snapshot

Phloroglucinol compounds of natural origin

inferredcites →https://doi.org/10.1055/s-2007-979533openalex-snapshot

Biologically Active and Other Chemical Constituents of the Herb ofHypericum perforatumL.

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-08-s(d)45openalex-snapshot

Convergent Synthesis of Fluorescence Labeled Solamin

inferredcites →https://doi.org/10.3987/com-08-s(d)64openalex-snapshot

Petiolins D and E, Phloroglucinol Derivatives from Hypericum pseudopetiolatum var. kiusianum

inferredcites →https://doi.org/10.3987/com-09-s(s)28openalex-snapshot

Biyouxanthones A - D, Prenylated Xanthones from Roots of Hypericum chinense

inferredcites →https://doi.org/10.7164/antibiotics.46.520openalex-snapshot

Biological activities of novel polyether antifungals, gambieric acids A and B from a marine dinoflagellate Gambierdiscus toxicus.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Structurally diverse polycyclic polyprenylated acylphloroglucinols with protective effect on human vein endothelial cells injured by high-glucose from Hypericum acmosepalum N. Robson

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.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/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/10.1007/978-3-030-52966-6_2openalex-snapshot

The Phytochemistry and Pharmacology of Hypericum

inferred← citeshttps://doi.org/10.1007/978-3-662-46402-1_4openalex-snapshot

Structure Elucidation Using Strict Structure Generation

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/10.1007/s13659-026-00629-9openalex-snapshot

Prenylated acylphloroglucinols from the fruits of Hypericum patulum

inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00007-3openalex-snapshot

Five-Membered Ring Systems: Furans and Benzofurans

inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00009-7openalex-snapshot

Five-Membered Ring Systems

inferred← citeshttps://doi.org/10.1016/b978-0-08-099406-2.00008-xopenalex-snapshot

Five-Membered Ring Systems

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.cclet.2020.04.028openalex-snapshot

Polycyclic polyprenylated acylphloroglucinol with an unprecedented spirocyclic core from Hypericum patulum

inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109458openalex-snapshot

Unprecedented sesquiterpene-polycyclic polyprenylated acylphloroglucinol adduct against acute myeloid leukemia via inhibiting mitochondrial complex V

inferred← citeshttps://doi.org/10.1016/j.cclet.2025.112069openalex-snapshot

Bioassay- and molecular network-guided discovery of PPAP derivatives from Hypericum monogynum with inhibitory activity against cardiac valve calcification

inferred← citeshttps://doi.org/10.1016/j.fitote.2012.08.022openalex-snapshot

Prenylated phloroglucinol derivatives from Hypericum sampsonii

inferred← citeshttps://doi.org/10.1016/j.fitote.2015.02.006openalex-snapshot

Antimicrobial and cytotoxic constituents from native Cameroonian medicinal plant Hypericum riparium

inferred← citeshttps://doi.org/10.1016/j.fitote.2021.105063openalex-snapshot

Hyperpatulones C-G, new spirocyclic polycyclic polyprenylated acylphloroglucinols from the leaves of Hypericum patulum

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.2015.02.009openalex-snapshot

Hyperascyrones A–H, polyprenylated spirocyclic acylphloroglucinol derivatives from Hypericum ascyron Linn.

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.phytochem.2018.12.005openalex-snapshot

Hyperbeanols F-Q, diverse monoterpenoid polyprenylated acylphloroglucinols from the flowers of Hypericum beanii

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.tetlet.2012.01.052openalex-snapshot

Biyoulactones D and E, meroterpenoids from Hypericum chinense

inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.06.045openalex-snapshot

Synthetic studies toward geranylated PPAP natural products oblongifolin A, oblongifolin D, and enervosanone

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/j.tetlet.2023.154361openalex-snapshot

Synthesis of the 5/6 fused-spiro tricyclic framework of manginoid A

inferred← citeshttps://doi.org/10.1016/s1875-5364(26)61170-3openalex-snapshot

Hypericum monogynum extract inhibits human aortic valve interstitial cell calcification by interfering with the EGFR/PI3K/AKT signaling pathway

inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00551openalex-snapshot

Research Progress of Polycyclic Polyprenylated Acylphloroglucinols

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00667openalex-snapshot

Polycyclic Polyprenylated Derivatives from Hypericum uralum: Neuroprotective Effects and Antidepressant-like Activity of Uralodin A

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00583openalex-snapshot

Spiro-Polycyclic Polyprenylated Acylphloroglucinols from Hypericum monogynum and Their anti-Alzheimer’s Disease Effects

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.0c02663openalex-snapshot

Solvent Effect in Gold(I)-Catalyzed Domino Reaction: Access to Furopyrans

inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03445openalex-snapshot

Discovering a Racemate Polycyclic Prenylated Acylphloroglucinol with Unprecedented Skeleton by an ESI-LCMS Analytical Approach

inferred← citeshttps://doi.org/10.1021/jacs.9b09344openalex-snapshot

Kinetic Resolution via Rh-Catalyzed C–C Activation of Cyclobutanones at Room Temperature

inferred← citeshttps://doi.org/10.1021/np500827hopenalex-snapshot

Prenylated Benzophenones from Triadenum japonicum

inferred← citeshttps://doi.org/10.1039/c2ob27073kopenalex-snapshot

Chemoenzymatic total synthesis of hyperiones A and B

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/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/c9ra00277dopenalex-snapshot

Hyperpatulones A–F, polycyclic polyprenylated acylphloroglucinols from Hypericum patulum and their cytotoxic activities

inferred← citeshttps://doi.org/10.1039/d1ob02107aopenalex-snapshot

Discovery of 13,15- nor -polycyclic polyprenylated acylphloroglucinols from Hypericum longistylum with anti-inflammatory activity

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Unprecedented nor-seco -polycyclic polyprenylated acylphloroglucinols counteract myocardial cell injury via activation of the Akt/mTOR signaling pathway

inferred← citeshttps://doi.org/10.1177/1934578x1400900720openalex-snapshot

Spirocyclic Acylphloroglucinol Derivatives from Hypericum pyramidatum

inferred← citeshttps://doi.org/10.1177/1934578x231164818openalex-snapshot

Chemical Constituents and Neuroprotective Activity of Hypericum hookerianum

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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