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

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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/cbdv.200900009openalex-snapshot

Polycyclic Polyprenylated Acylphloroglucinols and Chromone O‐Glucosides from Hypericum henryi subsp. uraloides

inferredcites →https://doi.org/10.1002/ejoc.201000284openalex-snapshot

Brasilamides A–D: Sesquiterpenoids from the Plant Endophytic Fungus Paraconiothyrium brasiliense

inferredcites →https://doi.org/10.1007/s002280050519openalex-snapshot

Adverse effects profile of the herbal antidepressant St. John's wort ( Hypericum perforatum L.)

inferredcites →https://doi.org/10.1007/s13659-014-0007-5openalex-snapshot

Hypercohones D–G, New Polycyclic Polyprenylated Acylphloroglucinol Type Natural Products from Hypericum cohaerens

inferredcites →https://doi.org/10.1016/0040-4020(57)88042-9openalex-snapshot

Chemical effects of steric strains—XIV

inferredcites →https://doi.org/10.1016/j.bmc.2015.08.028openalex-snapshot

Isolation and anticancer, anthelminthic, and antiviral (HIV) activity of acylphloroglucinols, and regioselective synthesis of empetrifranzinans from Hypericum roeperianum

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.phytochem.2015.02.009openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.phytochem.2016.02.003openalex-snapshot

Prenylated phenyl polyketides and acylphloroglucinols from Hypericum peplidifolium

inferredcites →https://doi.org/10.1016/j.phytol.2016.02.004openalex-snapshot

Cytotoxic polycyclic polyprenylated acylphloroglucinol derivatives and xanthones from Hypericum attenuatum

inferredcites →https://doi.org/10.1016/j.tet.2015.08.059openalex-snapshot

Cytotoxic polyprenylated acylphloroglucinol derivatives from Hypericum henryi

inferredcites →https://doi.org/10.1016/s0006-291x(05)80185-8openalex-snapshot

Antiretroviral activity of synthetic hypericin and related analogs

inferredcites →https://doi.org/10.1016/s0006-2952(02)01387-4openalex-snapshot

Hyperforin is a dual inhibitor of cyclooxygenase-1 and 5-lipoxygenase

inferredcites →https://doi.org/10.1016/s0022-3565(24)35043-8openalex-snapshot

Hyperforin, a Major Antidepressant Constituent of St. John’s Wort, Inhibits Serotonin Uptake by Elevating Free Intracellular Na+1 1

inferredcites →https://doi.org/10.1016/s0024-3205(98)00299-9openalex-snapshot

Hyperforin as a possible antidepressant component of hypericum extracts

inferredcites →https://doi.org/10.1016/s0040-4020(00)00010-7openalex-snapshot

Sampsoniones A–M, a Unique Family of Caged Polyprenylated Benzoylphloroglucinol Derivatives, from Hypericum sampsonii

inferredcites →https://doi.org/10.1016/s0957-4166(00)86328-4openalex-snapshot

Circular dichroism, XCIII determination of the absolute configuration of alcohols, olefins, epoxides, and ethers from the CD of their “in situ” complexes with [Rh2(O2CCF3)4].

inferredcites →https://doi.org/10.1016/s0957-4166(99)00115-9openalex-snapshot

[Rh2(OCOCF3)4] as an auxiliary chromophore in chiroptical studies on steroidal alcohols

inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00667openalex-snapshot

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

inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01063openalex-snapshot

Polycyclic Polyprenylated Acylphloroglucinol Congeners from Hypericum scabrum

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01178openalex-snapshot

Tricyclic Polyprenylated Acylphloroglucinols from St John’s Wort, Hypericum perforatum

inferredcites →https://doi.org/10.1021/acs.orglett.6b02725openalex-snapshot

Hypatulins A and B, Meroterpenes from Hypericum patulum

inferredcites →https://doi.org/10.1021/np200741xopenalex-snapshot

Prenylated Acylphloroglucinols, Chipericumins A–D, from Hypericum chinense

inferredcites →https://doi.org/10.1021/np50077a013openalex-snapshot

New Antimicrobial Filicinic Acid Derivatives from Hypericum drummondii

inferredcites →https://doi.org/10.1021/ol500808popenalex-snapshot

New Acylphloroglucinol Derivatives with Diverse Architectures from Hypericum henryi

inferredcites →https://doi.org/10.1055/s-2006-957437openalex-snapshot

Solubilized Hypericin and Pseudohypericin fromHypericum perforatumExert Antidepressant Activity in the Forced Swimming Test3

inferredcites →https://doi.org/10.3724/sp.j.1143.2008.00515openalex-snapshot

A New Polyisoprenylated Benzoylphloroglucinol Derivative from Hypericum henryi subsp. uraloides (Guttiferae

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.2022.113482zenodo-depositor-declared

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/slct.201903815openalex-snapshot

Isopropylpyrone and Phenylpyrones from the Leaves of Hypericum monogynum

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/s13659-026-00629-9openalex-snapshot

Prenylated acylphloroglucinols from the fruits of Hypericum patulum

inferred← citeshttps://doi.org/10.1016/b978-0-443-15628-1.00005-2openalex-snapshot

Acylphloroglucinols with anticancer and/or antimalarial activities—An overview

inferred← citeshttps://doi.org/10.1016/j.cclet.2019.10.014openalex-snapshot

Hyperinoids A and B, two polycyclic meroterpenoids from 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.ejmech.2022.114532openalex-snapshot

Discovery of dearomatized isoprenylated acylphloroglucinols with colon tumor suppressive activities in mice via inhibiting NFκB-FAT1-PDCD4 signaling activation

inferred← citeshttps://doi.org/10.1021/acs.jafc.2c04216openalex-snapshot

Polyprenylated Benzophenones and Tocotrienol Derivatives from the Edible Fruits of Garcinia oblongifolia Champ. ex Benth. and Their Cytotoxicity Activity

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04135openalex-snapshot

Isolation and Biomimetic Semisynthesis of Hyperzrones A and B, Two Nor-Polycyclic Polyprenylated Acylphloroglucinols with a Characteristic Cyclobutane Moiety, from Hypericum beanii

inferred← citeshttps://doi.org/10.1039/d0qo00152jopenalex-snapshot

Hyperforones A–C, benzoyl-migrated [5.3.1]-type polycyclic polyprenylated acylphloroglucinols from Hypericum forrestii

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/molecules29133075openalex-snapshot

New Monoterpenoid Glycosides from the Fruits of Hypericum patulum Thunb.

inferred← citeshttps://doi.org/10.3390/molecules31173072openalex-snapshot

New Stilbene Dimer Compounds from the Fruits of Hypericum patulum and Their Antioxidant and Anti-α-Glucosidase Activities

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