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Tricyclic Polyprenylated Acylphloroglucinols from St John’s Wort, Hypericum perforatum
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9783527688166openalex-snapshot
Organic Stereochemistry: Experimental and Computational Methods
inferredcites →https://doi.org/10.1002/anie.200605207openalex-snapshot
Phloroglucinol Derivatives Guttiferone G, Aristoforin, and Hyperforin: Inhibitors of Human Sirtuins SIRT1 and SIRT2
inferredcites →https://doi.org/10.1002/anie.200906678openalex-snapshot
Catalytic Asymmetric Total Synthesis of ent‐Hyperforin
inferredcites →https://doi.org/10.1002/ardp.19953281007openalex-snapshot
Peroxides as Constituents of Plants, Part 19: A C50‐Hydroperoxide from Hypericum perforatum
inferredcites →https://doi.org/10.1002/cbdv.201300399openalex-snapshot
In vitro Growth Inhibition by Hypericum Extracts and Isolated Pure Compounds of Paenibacillus larvae, a Lethal Disease Affecting Honeybees Worldwide
inferredcites →https://doi.org/10.1002/da.20036openalex-snapshot
Assessing patient beliefs in a clinical trial ofHypericum perforatum in major depression
inferredcites →https://doi.org/10.1002/ijc.21246openalex-snapshot
Hyperforin, a bio‐active compound of St. John's Wort, is a new inhibitor of angiogenesis targeting several key steps of the process
inferredcites →https://doi.org/10.1002/jcc.21460openalex-snapshot
Accurate conformation‐dependent molecular electrostatic potentials for high‐throughput in silico drug discovery
inferredcites →https://doi.org/10.1007/s002130000625openalex-snapshot
St. John's wort (Hypericum perforatum): a review of the current pharmacological, toxicological, and clinical literature
inferredcites →https://doi.org/10.1007/s11816-010-0159-7openalex-snapshot
Biotechnological improvement of lignocellulosic feedstock for enhanced biofuel productivity and processing
inferredcites →https://doi.org/10.1016/0006-2952(61)90145-9openalex-snapshot
A new and rapid colorimetric determination of acetylcholinesterase activity
inferredcites →https://doi.org/10.1016/j.canlet.2004.01.031openalex-snapshot
Hypericum perforatum methanolic extract inhibits growth of human prostatic carcinoma cell line orthotopically implanted in nude mice
inferredcites →https://doi.org/10.1016/j.indcrop.2014.05.018openalex-snapshot
Methanolic extract of Hypericum perforatum cells elicited with Agrobacterium tumefaciens provides protection against oxidative stress induced in human HepG2 cells
inferredcites →https://doi.org/10.1016/j.jep.2009.10.011openalex-snapshot
Investigations on the in vivo wound healing potential of Hypericum perforatum L.
inferredcites →https://doi.org/10.1016/j.neuropharm.2006.09.003openalex-snapshot
Standardized Hypericum perforatum reduces oxidative stress and increases gene expression of antioxidant enzymes on rotenone-exposed rats
inferredcites →https://doi.org/10.1016/j.phytochem.2006.09.018openalex-snapshot
Hyperforin and its analogues inhibit CYP3A4 enzyme activity
inferredcites →https://doi.org/10.1016/j.phytochem.2007.01.001openalex-snapshot
Biosynthesis of hyperforin and adhyperforin from amino acid precursors in shoot cultures of Hypericum perforatum
inferredcites →https://doi.org/10.1016/j.phytochem.2007.06.004openalex-snapshot
Differential accumulation of hyperforin and secohyperforin in Hypericum perforatum tissue cultures
inferredcites →https://doi.org/10.1016/j.phytochem.2012.02.002openalex-snapshot
Benzophenone synthase from Garcinia mangostana L. pericarps
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.tet.2016.06.035openalex-snapshot
Hyperhexanone A, a crucial intermediate from bicyclo[3.3.1]- to cyclohexanone monocyclic-polycyclic polyprenylated acylphloroglucinols
inferredcites →https://doi.org/10.1016/j.tetlet.2004.11.007openalex-snapshot
A phloroglucinol derivative with a new carbon skeleton from Hypericum perforatum (Guttiferae)
inferredcites →https://doi.org/10.1016/j.tetlet.2015.02.056openalex-snapshot
Two new adamantyl-like polyprenylated acylphloroglucinols from Hypericum attenuatum choisy
inferredcites →https://doi.org/10.1016/s0024-3205(02)01566-7openalex-snapshot
St. John's wort and depression
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/s0031-9422(97)00903-5openalex-snapshot
Oxidation products of hyperforin from Hypericum perforatum
inferredcites →https://doi.org/10.1016/s0076-6879(97)77018-6openalex-snapshot
[16] SHELXL: High-resolution refinement
inferredcites →https://doi.org/10.1016/s0165-6147(00)01716-8openalex-snapshot
St John's wort: Prozac from the plant kingdom
inferredcites →https://doi.org/10.1016/s0300-483x(97)00151-0openalex-snapshot
The sensitivity and specificity of the MTS tetrazolium assay for detecting the in vitro cytotoxicity of 20 chemicals using human cell lines
inferredcites →https://doi.org/10.1016/s0367-326x(03)00114-xopenalex-snapshot
Further degradation product of hyperforin from Hypericum perforatum (St. John's Wort)
inferredcites →https://doi.org/10.1016/s0893-133x(00)00102-0openalex-snapshot
Inhibition of Synaptosomal Uptake of 3H-L-glutamate and 3H-GABA by Hyperforin, a Major Constituent of St. John's Wort The Role of Amiloride Sensitive Sodium Conductive Pathways
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/10.1016/s0960-894x(99)00589-2openalex-snapshot
Phenanthrenequinone antiretroviral agents
inferredcites →https://doi.org/10.1021/acs.jnatprod.5b01055openalex-snapshot
Natural Products as Sources of New Drugs from 1981 to 2014
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00754openalex-snapshot
Skeleton Reassignment of Type C Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/ci6005646openalex-snapshot
Generating Conformer Ensembles Using a Multiobjective Genetic Algorithm
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/jf049571ropenalex-snapshot
Antioxidant Activity of a Flavonoid-Rich Extract of Hypericum perforatum L . in Vitro
inferredcites →https://doi.org/10.1021/jf052344kopenalex-snapshot
Evaluation of the Light-Sensitive Cytotoxicity of Hypericum perforatum Extracts, Fractions, and Pure Compounds
inferredcites →https://doi.org/10.1021/jf0710074openalex-snapshot
Inhibition of Prostaglandin E2 Production by Anti-inflammatory Hypericum perforatum Extracts and Constituents in RAW264.7 Mouse Macrophage Cells
inferredcites →https://doi.org/10.1021/jm0209782openalex-snapshot
Biosynthesis of Hyperforin in Hypericum perforatum
inferredcites →https://doi.org/10.1021/np000362kopenalex-snapshot
Three New Hyperforin Analogues from Hypericum perforatum
inferredcites →https://doi.org/10.1021/np049811xopenalex-snapshot
Anti-inflammatory Phloroglucinols and Terpenoids from Garcinia subelliptica
inferredcites →https://doi.org/10.1021/np400134zopenalex-snapshot
Benzophenone Glycosides from Hypericum humifusum ssp. austral
inferredcites →https://doi.org/10.1021/np400287ropenalex-snapshot
Bioactive Polyprenylated Acylphloroglucinol Derivatives from Hypericum cohaerens
inferredcites →https://doi.org/10.1021/np980470vopenalex-snapshot
Furohyperforin, a Prenylated Phloroglucinol from St. John's Wort (Hypericum perforatum)
inferredcites →https://doi.org/10.1021/np9903752openalex-snapshot
Hyperforin Analogues from St. John's Wort (Hypericum perforatum)
inferredcites →https://doi.org/10.1021/ol500808popenalex-snapshot
New Acylphloroglucinol Derivatives with Diverse Architectures from Hypericum henryi
inferredcites →https://doi.org/10.1021/ol5030579openalex-snapshot
Bioactive Acylphloroglucinols with Adamantyl Skeleton from Hypericum sampsonii
inferredcites →https://doi.org/10.1038/sj.onc.1205190openalex-snapshot
Inhibition of tumour cell growth by hyperforin, a novel anticancer drug from St. John's wort that acts by induction of apoptosis
inferredcites →https://doi.org/10.1038/srep14772openalex-snapshot
Hyperisampsins H–M, Cytotoxic Polycyclic Polyprenylated Acylphloroglucinols from Hypericum sampsonii
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/10.1039/c4np00027gopenalex-snapshot
Structural diversity and bioactivities of natural benzophenones
inferredcites →https://doi.org/10.1039/c4ra11675eopenalex-snapshot
Hyperattenins A–I, bioactive polyprenylated acylphloroglucinols from Hypericum attenuatum Choisy
inferredcites →https://doi.org/10.1039/c6ra17885eopenalex-snapshot
Sampbenzophenones A–G, prenylated benzoylphloroglucinol derivatives from Hypericum sampsonii
inferredcites →https://doi.org/10.1055/s-0033-1351019openalex-snapshot
Topical Application of St. Johnʼs Wort (Hypericum perforatum)
inferredcites →https://doi.org/10.1055/s-2005-873127openalex-snapshot
The Lipophilic Extract ofHypericum perforatumExerts Significant Cytotoxic Activity Against T24 and NBT-II Urinary Bladder Tumor Cells
inferredcites →https://doi.org/10.1055/s-2007-979341openalex-snapshot
Hyperforin Represents the Neurotransmitter Reuptake Inhibiting Constituent of Hypericum Extract
inferredcites →https://doi.org/10.1056/nejm200012283432607openalex-snapshot
Managing Depression in Medical Outpatients
inferredcites →https://doi.org/10.1056/nejm2003ra020003openalex-snapshot
Alzheimer's Disease and Parkinson's Disease
inferredcites →https://doi.org/10.1073/pnas.85.14.5230openalex-snapshot
Therapeutic agents with dramatic antiretroviral activity and little toxicity at effective doses: aromatic polycyclic diones hypericin and pseudohypericin.
inferredcites →https://doi.org/10.1073/pnas.90.1.158openalex-snapshot
Photodynamic inactivation of infectivity of human immunodeficiency virus and other enveloped viruses using hypericin and rose bengal: inhibition of fusion and syncytia formation.
inferredcites →https://doi.org/10.1093/oxfordjournals.aje.a118408openalex-snapshot
A SIMPLE METHOD OF ESTIMATING FIFTY PER CENT ENDPOINTS12
inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot
On enantiomorph-polarity estimation
inferredcites →https://doi.org/10.1189/jlb.0707469openalex-snapshot
Hyperforin down-regulates effector function of activated T lymphocytes and shows efficacy against Th1-triggered CNS inflammatory-demyelinating disease
inferredcites →https://doi.org/10.1211/0022357011775910openalex-snapshot
St John's wort ( Hypericum perforatum L.): a review of its chemistry, pharmacology and clinical properties
inferredcites →https://doi.org/10.1248/cpb.56.1164openalex-snapshot
Prenylated Phloroglucinol Derivatives from Hypericum perforatum var. angustifolium
inferredcites →https://doi.org/10.2165/00023210-200317080-00001openalex-snapshot
Mechanism of Action of St John???s Wort in Depression
inferredcites →https://doi.org/10.2174/092986710790226156openalex-snapshot
Neurobiological Effects of Hyperforin and its Potential in Alzheimers Disease Therapy
inferredcites →https://doi.org/10.2174/1871527311312050013openalex-snapshot
Neuroprotective Properties of Standardized Extracts of Hypericum perforatum on Rotenone Model of Parkinson’s Disease
inferredcites →https://doi.org/10.3390/m158openalex-snapshot
A New Heterocyclization Product of Adhyperforin from Hypericum perforatum (St. John's Wort)
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/cbdv.201800395openalex-snapshot
Polyketide and Prenylxanthone Derivatives from the Endophytic Fungus Aspergillus sp. TJ23
inferred← citeshttps://doi.org/10.1002/cbdv.202100897openalex-snapshot
A New Lignan and C(6)‐Oxygenated Flavonoids from the Inflorescence of Ambrosia artemisiifolia
inferred← citeshttps://doi.org/10.1002/cjoc.202100468openalex-snapshot
Hybeanones A and B, Two Highly Modified Polycyclic Polyprenylated Acylphloroglucinols from Hypericum beanii
inferred← citeshttps://doi.org/10.1002/slct.201903815openalex-snapshot
Isopropylpyrone and Phenylpyrones from the Leaves of Hypericum monogynum
inferred← citeshttps://doi.org/10.1007/s10600-025-04630-5openalex-snapshot
Cytotoxic Polyprenylated Acylphloroglucinols from Hypericum uralum
inferred← citeshttps://doi.org/10.1016/j.arabjc.2022.104057openalex-snapshot
Bioassay and UPLC-Q-Orbitrap-MS/MS guided isolation of polycyclic polyprenylated acylphloroglucinols from St. John's wort and their neuroprotective activity
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.2021.105144openalex-snapshot
Polycyclic polyprenylated acylphloroglucinols with immunosuppressive activity from Hypericum perforatum and absolute configurations assignment of previously reported analogues
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109134openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols from Hypericum Hookerianum with their immunosuppressive activities
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.110478openalex-snapshot
Hyperforatone A, the 1,8-seco rearranged polycyclic polyprenylated acylphloroglucinol with a unique bicyclo[5.4.0]undecane core from Hypericum perforatum
inferred← citeshttps://doi.org/10.1016/j.cclet.2025.111580openalex-snapshot
Hypertaxoids A and B, two unique meroterpenoids from Hypericum elatoides as microtubule stabilizers and their antiproliferative effects on cervical cancer
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117401openalex-snapshot
Phytomolecules as Alzheimer's therapeutics: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.09.020openalex-snapshot
New phloroglucinol derivatives from the whole plant of Hypericum uralum
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.12.020openalex-snapshot
Hyperattenins L and M, two new polyprenylated acylphloroglucinols with adamantyl and homoadamantyl core structures from Hypericum attenuatum
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104535openalex-snapshot
Hyperacmosins E-G, three new homoadamantane-type polyprenylated acylphloroglucinols from Hypericum acmosepalum
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104550openalex-snapshot
Polycyclic polyprenylated acylphloroglucinols with acetylcholinesterase inhibitory activities from Hypericum perforatum
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104685openalex-snapshot
New cytotoxic secondary metabolites against human pancreatic cancer cells from the Hypericum perforatum endophytic fungus Aspergillus terreus
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105221openalex-snapshot
(±)-Hyperpyran A: Terpenoid-based bicyclic dihydropyran enantiomers with hypoglycemic activity from Hypericum perforatum (St. John's wort)
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105249openalex-snapshot
Bioactive polycyclic polyprenylated acylphloroglucinols from Hypericum scabrum
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106493openalex-snapshot
Monocyclic and polycyclic polyprenylated acylphloroglucinols with anti-steatohepatitis effect from the pericarps of Garcinia multiflora
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.12.231openalex-snapshot
Inhibition of pancreatic lipase by the constituents in St. John's Wort: In vitro and in silico investigations
inferred← citeshttps://doi.org/10.1016/j.jep.2020.112948openalex-snapshot
Chemical constituents with cytotoxic and anti-inflammatory activity in Hypericum sampsonii and the antitumor potential under the view of cancer-related inflammation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.04.011openalex-snapshot
Hyperforatins L–U: Prenylated acylphloroglucinols with a terminal double bond from Hypericum perforatum L. (St John's Wort)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112290openalex-snapshot
Metabolomic fingerprinting and genetic discrimination of four Hypericum taxa from Greece
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113413openalex-snapshot
Polycyclic polyprenylated acylphloroglucinols from Hypericum beanii and their hepatoprotective activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114047openalex-snapshot
Hyperatins A–D, highly oxidized polycyclic polyprenylated acylphloroglucinols from Hypericum perforatum L. with hypoglycemic potential in liver cells
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114242openalex-snapshot
Polycyclic polyprenylated acylphloroglucinols from the pericarps of Garcinia multiflora champ. ex Benth. with cytotoxic property
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114450openalex-snapshot
Hypertums A−J, bioactive polycyclic polyprenylated acylphloroglucinols with diverse skeletons from Hypericum perforatum L. (St. John's wort)
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00551openalex-snapshot
Research Progress of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00889openalex-snapshot
Protoilludane, Illudalane, and Botryane Sesquiterpenoids from the Endophytic Fungus Phomopsis sp. TJ507A
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00176openalex-snapshot
Methylated Polycyclic Polyprenylated Acylphloroglucinol Derivatives from Hypericum ascyron
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01187openalex-snapshot
Hypersonins A–D, Polycyclic Polyprenylated Acylphloroglucinols with a 1,2-seco-Homoadamantane Architecture from Hypericum wilsonii
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02853openalex-snapshot
Longisglucinols A–C, Structurally Intriguing Polycyclic Polyprenylated Acylphloroglucinols with Anti-inflammatory Activity from Hypericum longistylum
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03078openalex-snapshot
Me2AlSEt-Promoted Domino Dieckmann Cyclization Enables the Total Synthesis of Polycyclic Polyprenylated Acylphloroglucinols
inferred← citeshttps://doi.org/10.1038/s41598-026-49336-yopenalex-snapshot
Tertiary alcohol-containing polycyclic polyprenylated acylphloroglucinols from Hypericum scabrum inhibit the proliferation of oral squamous cell carcinoma CAL-27 cells
inferred← citeshttps://doi.org/10.1039/c8ob02067aopenalex-snapshot
Bioactive polycyclic polyprenylated acylphloroglucinols from Hypericum perforatum
inferred← citeshttps://doi.org/10.1039/c8qo01268gopenalex-snapshot
Highly functionalized cyclohexanone-monocyclic polyprenylated acylphloroglucinols from Hypericum perforatum induce leukemia cell apoptosis
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/c9qo01158gopenalex-snapshot
Wilsonglucinols A–C, homoadamantane-type polycyclic polyprenylated acylphloroglucinols with unusual fused epoxy ring skeletons from Hypericum wilsonii
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/d0qo00259copenalex-snapshot
Discovery of new polycyclic polyprenylated acylphloroglucinols with diverse architectures as potent cyclooxygenase-2 inhibitors
inferred← citeshttps://doi.org/10.1039/d1qo00271fopenalex-snapshot
Norwilsonnol A, an immunosuppressive polycyclic polyprenylated acylphloroglucinol with a spiro[5-oxatricyclo[6.4.0.0 3,7 ]dodecane-6′,1-1′,2′-dioxane] system from Hypericum wilsonii
inferred← citeshttps://doi.org/10.1039/d1ra03533aopenalex-snapshot
Hyperacmosins K–M, three new polycyclic polyprenylated acylphloroglucinols from Hypericum acmosepalum
inferred← citeshttps://doi.org/10.1039/d1sc03356eopenalex-snapshot
Unprecedented polycyclic polyprenylated acylphloroglucinols with anti-Alzheimer's activity from St. John's wort
inferred← citeshttps://doi.org/10.1039/d4qo00444bopenalex-snapshot
(±)-Hypandrone A, a pair of polycyclic polyprenylated acylphloroglucinol enantiomers with a caged 7/6/5/6/6 pentacyclic skeleton from Hypericum androsaemum
inferred← citeshttps://doi.org/10.1039/d4qo01010hopenalex-snapshot
Unprecedented nor-seco -polycyclic polyprenylated acylphloroglucinols counteract myocardial cell injury via activation of the Akt/mTOR signaling pathway
inferred← citeshttps://doi.org/10.1080/10286020.2020.1739662openalex-snapshot
Hyperacmosins H-J, three new polycyclic polyprenylated acylphloroglucinol derivatives from Hypericum acmosepalum
inferred← citeshttps://doi.org/10.1080/10286020.2021.2016716openalex-snapshot
Four new polyprenylated acylphloroglucinol derivatives from Hypericum beanii
inferred← citeshttps://doi.org/10.1080/1040841x.2022.2036100openalex-snapshot
Photoactivity of hypericin: from natural product to antifungal application
inferred← citeshttps://doi.org/10.1080/14786419.2018.1539983openalex-snapshot
A new cytotoxic polycyclic polyprenylated acylphloroglucinol from Garcinia nujiangensis screened by the LC-PDA and LC-MS
inferred← citeshttps://doi.org/10.1080/14786419.2023.2278176openalex-snapshot
Hyperipersions A-C, three new acylphloroglucinols from the branches and leaves of Hypericum perforatum L. with antiangiogenic activities
inferred← citeshttps://doi.org/10.2174/1389557519666190926120211openalex-snapshot
Hypericum spp.: An Update on the Biological Activities and Metabolic Profiles
inferred← citeshttps://doi.org/10.3389/fphar.2020.00397openalex-snapshot
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes
inferred← citeshttps://doi.org/10.3389/fphar.2023.1247675openalex-snapshot
Hypericum sampsonii Hance: a review of its botany, traditional uses, phytochemistry, biological activity, and safety
inferred← citeshttps://doi.org/10.3390/molecules23030683openalex-snapshot
Hyperjaponol H, A New Bioactive Filicinic Acid-Based Meroterpenoid from Hypericum japonicum Thunb. ex Murray
inferred← citeshttps://doi.org/10.3390/molecules25246034openalex-snapshot
New Cyclic Diarylheptanoids from Platycarya strobilacea
inferred← citeshttps://doi.org/10.3390/molecules26226955openalex-snapshot
Regioisomers Salviprolin A and B, Unprecedented Rosmarinic Acid Conjugated Dinorditerpenoids from Salvia przewalskii Maxim
inferred← citeshttps://doi.org/10.3390/molecules27185932openalex-snapshot
Hyperacmosin R, a New Decarbonyl Prenylphloroglucinol with Unusual Spiroketal Subunit from Hypericum acmosepalum
inferred← citeshttps://doi.org/10.3390/molecules29081756openalex-snapshot
Four New Polyprenylated Acylphloroglucinols from Hypericum perforatum L.
inferred← citeshttps://doi.org/10.3390/ph18101591openalex-snapshot
Polyprenylated Acylphloroglucinols from Hypericum rochelii and Hypericum olympicum—Cytotoxic Effects on Non-Tumorigenic Cell Lines and Antibacterial Potential
inferred← citeshttps://doi.org/10.3390/pharmaceutics17030336openalex-snapshot
An Overview of the Bioactivity of Spontaneous Medicinal Plants Suitable for the Improvement of Lung Cancer Therapies
inferred← citeshttps://doi.org/10.3390/plants11192509openalex-snapshot
Hypericum Genus as a Natural Source for Biologically Active Compounds
inferred← citeshttps://doi.org/10.3390/plants12071500openalex-snapshot
Cytotoxic and Antibacterial Prenylated Acylphloroglucinols from Hypericum olympicum L.
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