On the public citation graph

Diverse Polycyclic Polyprenylated Acylphloroglucinol Congeners with Anti-Nonalcoholic Steatohepatitis Activity from Hypericum forrestii

0 signed · 91 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9783527634606.ch12openalex-snapshot
Polyprenylated Phloroglucinols and Xanthones
inferredcites →https://doi.org/10.1002/anie.201404437openalex-snapshot
Asymmetric, Stereodivergent Synthesis of (−)‐Clusianone Utilizing a Biomimetic Cationic Cyclization
inferredcites →https://doi.org/10.1002/anie.201812909openalex-snapshot
Total Synthesis and Anticancer Activity of (+)‐Hypercalin C and Congeners
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/hep.30300openalex-snapshot
DEAD Box Protein 5 Inhibits Liver Tumorigenesis by Stimulating Autophagy via Interaction with p62/SQSTM1
inferredcites →https://doi.org/10.1002/hlca.19890720820openalex-snapshot
New Cell Growth‐Inhibitory Cyclohexadienone Derivatives from Hypericum calycinum L.
inferredcites →https://doi.org/10.1002/hlca.200390173openalex-snapshot
Polyprenylated Phloroglucinol Derivatives from Hypericum sampsonii
inferredcites →https://doi.org/10.1007/s00018-018-2947-0openalex-snapshot
Molecular pathways of nonalcoholic fatty liver disease development and progression
inferredcites →https://doi.org/10.1007/s11426-016-0052-4openalex-snapshot
Polyprenylated acylphloroglucinols from the fruits of Hypericum henryi
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/10.1007/s13659-019-00229-wopenalex-snapshot
Dearomatized Isoprenylated Acylphloroglucinol Derivatives with Potential Antitumor Activities from Hypericum henryi
inferredcites →https://doi.org/10.1007/s13659-020-00245-1openalex-snapshot
Adipogenesis Inhibitory Activity of Hypersampsone P from Hypericum subsessile
inferredcites →https://doi.org/10.1016/j.bioorg.2019.103075openalex-snapshot
Human neutrophil elastase (HNE) inhibitory polyprenylated acylphloroglucinols from the flowers of Hypericum ascyron
inferredcites →https://doi.org/10.1016/j.fitote.2014.02.011openalex-snapshot
Cytotoxic polycyclic polyprenylated acylphloroglucinols from Hypericum attenuatum
inferredcites →https://doi.org/10.1016/j.jep.2020.112686openalex-snapshot
Ethnopharmacology of Hypericum species in China: A comprehensive review on ethnobotany, phytochemistry and pharmacology
inferredcites →https://doi.org/10.1016/j.phymed.2020.153294openalex-snapshot
Physalin D attenuates hepatic stellate cell activation and liver fibrosis by blocking TGF-β/Smad and YAP signaling
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.2018.08.002openalex-snapshot
Structural diversity and biological activities of phloroglucinol derivatives from Hypericum species
inferredcites →https://doi.org/10.1016/j.tet.2005.06.030openalex-snapshot
Structural revision of clusianone and 7-epi-clusianone and anti-HIV activity of polyisoprenylated benzophenones
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.tetasy.2017.09.015openalex-snapshot
Features of electronic circular dichroism and tips for its use in determining absolute configuration
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/j.tetlet.2015.08.033openalex-snapshot
Hypercohin K, a polycyclic polyprenylated acylphloroglucinol with an unusual spiro-fused cyclopropane ring from Hypericum cohaerens
inferredcites →https://doi.org/10.1016/j.tetlet.2017.04.044openalex-snapshot
seco-Polycyclic polyprenylated acylphloroglucinols with unusual carbon skeletons from Hypericum ascyron
inferredcites →https://doi.org/10.1016/j.tetlet.2018.09.071openalex-snapshot
Spirocyclic polycyclic polyprenylated acylphloroglucinols from the ethyl acetate fraction of Hypericum henryi
inferredcites →https://doi.org/10.1016/s0040-4020(98)01203-4openalex-snapshot
Prenylated benzophenone derivatives from Caribbean Clusia species (Guttiferae). Plukenetiones B-G and xerophenone A
inferredcites →https://doi.org/10.1016/s0040-4039(00)00832-7openalex-snapshot
On the structures of plukenetiones B, D, and E and their relationships to other polycyclic polyprenylated acylphloroglucinols
inferredcites →https://doi.org/10.1016/s1875-5364(20)30044-3openalex-snapshot
New meroterpenoids and C-methylated flavonoid isolated from Baeckea frutescens
inferredcites →https://doi.org/10.1021/acs.chemrev.7b00551openalex-snapshot
Research Progress of Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/acs.jmedchem.0c00618openalex-snapshot
Design and Structural Optimization of Dual FXR/PPARδ Activators
inferredcites →https://doi.org/10.1021/acs.jmedchem.9b01701openalex-snapshot
The Race to Bash NASH: Emerging Targets and Drug Development in a Complex Liver Disease
inferredcites →https://doi.org/10.1021/acs.jmedchem.9b02056openalex-snapshot
Congenetic Hybrids Derived from Dearomatized Isoprenylated Acylphloroglucinol with Opposite Effects on Cav3.1 Low Voltage-Gated Ca2+ Channel
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.5b00066openalex-snapshot
Hypermongones A–J, Rare Methylated Polycyclic Polyprenylated Acylphloroglucinols from the Flowers of Hypericum monogynum
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.5b00830openalex-snapshot
1,9-seco-Bicyclic Polyprenylated Acylphloroglucinols from Hypericum uralum
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.9b00354openalex-snapshot
Hypascyrins A–E, Prenylated Acylphloroglucinols from Hypericum ascyron
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b01285openalex-snapshot
Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019
inferredcites →https://doi.org/10.1021/acs.orglett.6b02725openalex-snapshot
Hypatulins A and B, Meroterpenes from Hypericum patulum
inferredcites →https://doi.org/10.1021/acs.orglett.9b03098openalex-snapshot
Hyperberins A and B, Type B Polycyclic Polyprenylated Acylphloroglucinols with Bicyclo[5.3.1]hendecane Core from Hypericum beanii
inferredcites →https://doi.org/10.1021/cr0500582openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/cr200055gopenalex-snapshot
Semipinacol Rearrangement in Natural Product Synthesis
inferredcites →https://doi.org/10.1021/jacs.6b09727openalex-snapshot
Syntheses of (+)-30-epi-, (−)-6-epi-, (±)-6,30-epi-13,14-Didehydroxyisogarcinol and (±)-6,30-epi-Garcimultiflorone A Utilizing Highly Diastereoselective, Lewis Acid-Controlled Cyclizations
inferredcites →https://doi.org/10.1021/jo048857sopenalex-snapshot
Modulation of Chemoselectivity by Protein Additives. Remarkable Effects in the Oxidation of Hyperforin
inferredcites →https://doi.org/10.1021/jo500027kopenalex-snapshot
Biomimetic Total Synthesis of (±)-Doitunggarcinone A and (+)-Garcibracteatone
inferredcites →https://doi.org/10.1021/np400287ropenalex-snapshot
Bioactive Polyprenylated Acylphloroglucinol Derivatives from Hypericum cohaerens
inferredcites →https://doi.org/10.1021/np980339nopenalex-snapshot
A Polyisoprenylated Benzophenone from Cuban Propolis
inferredcites →https://doi.org/10.1021/np9903752openalex-snapshot
Hyperforin Analogues from St. John's Wort (Hypericum perforatum)
inferredcites →https://doi.org/10.1021/ol302524qopenalex-snapshot
Biomimetic Total Synthesis of (±)-Garcibracteatone
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/ol9907825openalex-snapshot
Cytotoxic Polyprenylated Benzoylphloroglucinol Derivatives with an Unusual Adamantyl Skeleton from Hypericum sampsonii (Guttiferae)
inferredcites →https://doi.org/10.1038/nchem.2479openalex-snapshot
Counting on natural products for drug design
inferredcites →https://doi.org/10.1038/nrd.2017.146openalex-snapshot
Directing evolution: the next revolution in drug discovery?
inferredcites →https://doi.org/10.1038/nrd.2018.116openalex-snapshot
Expanding the medicinal chemistry synthetic toolbox
inferredcites →https://doi.org/10.1038/s41591-018-0104-9openalex-snapshot
Mechanisms of NAFLD development and therapeutic strategies
inferredcites →https://doi.org/10.1039/c8ob02067aopenalex-snapshot
Bioactive polycyclic polyprenylated acylphloroglucinols from Hypericum perforatum
inferredcites →https://doi.org/10.1039/c9cc09433dopenalex-snapshot
Taxodisones A and B: bioactive C 30 -terpenes with new skeletons from Taxodium distichum and their biosynthetic origin
inferredcites →https://doi.org/10.1039/c9ob01500kopenalex-snapshot
Przewalcyrones A–F, epoxychromene-containing polycyclic polyprenylated acylphloroglucinols with immunosuppressive activity from Hypericum przewalskii Maxim.
inferredcites →https://doi.org/10.1039/d0qo00152jopenalex-snapshot
Hyperforones A–C, benzoyl-migrated [5.3.1]-type polycyclic polyprenylated acylphloroglucinols from Hypericum forrestii
inferredcites →https://doi.org/10.1039/d0qo00259copenalex-snapshot
Discovery of new polycyclic polyprenylated acylphloroglucinols with diverse architectures as potent cyclooxygenase-2 inhibitors
inferredcites →https://doi.org/10.1074/jbc.m011538200openalex-snapshot
The Desymmetrization of Bicyclic β-Diketones by an Enzymatic Retro-Claisen Reaction
inferredcites →https://doi.org/10.1136/gutjnl-2016-312431openalex-snapshot
Current and upcoming pharmacotherapy for non-alcoholic fatty liver disease
inferredcites →https://doi.org/10.3390/cells9010037openalex-snapshot
Anti-NASH Drug Development Hitches a Lift on PPAR Agonism
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.2022.113166zenodo-depositor-declared
Kiiacylphnols A−H, eight undescribed polycyclic polyprenylated acylphloroglucinols with anticancer activities from Hypericum przewalskii Maxim
inferred← citeshttps://doi.org/10.1002/chem.202401908openalex-snapshot
Unique Reactivity of the 1,4‐Bis(silyloxy)‐1,3‐cyclopentadiene Moiety: Application to the Synthesis of 7‐Norbornanone Derivatives
inferred← citeshttps://doi.org/10.1002/chir.23393openalex-snapshot
ECD exciton chirality method today: a modern tool for determining absolute configurations
inferred← citeshttps://doi.org/10.1002/cjoc.202400739openalex-snapshot
Hyperkouytones A—O, New Polyprenylated Acylphloroglucinols from Hypericum kouytchense with Multidrug Resistance Reversal Activity
inferred← citeshttps://doi.org/10.1002/hep.32651openalex-snapshot
RNA helicase DEAD‐box protein 5 alleviates nonalcoholic steatohepatitis progression via tethering TSC complex and suppressing mTORC1 signaling
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106005openalex-snapshot
Diverse polycyclic polyprenylated acylphloroglucinols with anti-neuroinflammatory activity from Hypericum beanii
inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.110638openalex-snapshot
Structurally diverse polyprenylated acylphloroglucinols from Hypericum addingtonii with anti-hepatocellular carcinoma activity
inferred← citeshttps://doi.org/10.1016/j.cclet.2021.11.011openalex-snapshot
Hyperbenzones A and B, two 1,2-seco and rearranged polycyclic polyprenylated acylphloroglucinols from Hypericum beanii
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105389openalex-snapshot
Hyperxylones A and B, two polycyclic polyprenylated acylphloroglucinols with a benzoyl substituted bicyclo[3.2.1]octane core from Hypericum beanii
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.lfs.2024.123031openalex-snapshot
Identification of protein partners for small molecules reshapes the understanding of nonalcoholic steatohepatitis and drug discovery
inferred← citeshttps://doi.org/10.1016/j.phymed.2025.157159openalex-snapshot
Hyperacmotone A alleviates Non-alcoholic Steatohepatitis via regulating PPARα signaling
inferred← citeshttps://doi.org/10.1016/j.phymed.2026.157936openalex-snapshot
Hypercohin A alleviates hepatic steatosis via the mammalian target of rapamycin (mTOR)-dependent suppression of de novo lipogenesis and ferroptosis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114167openalex-snapshot
Garciyunnanones A–R: Caged polycyclic polyprenylated acylphloroglucinols decorated with a lavandulyl substituent from Garcinia yunnanensis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153987openalex-snapshot
In(OTf)3 catalyzed regioselective acyloin rearrangement of 1-acyl-1-indanols
inferred← citeshttps://doi.org/10.1016/s1875-5364(22)60199-7openalex-snapshot
Diverse sesquiterpenoids from Litsea lancilimba Merr. with potential neuroprotective effects against H2O2-induced SH-SY5Y cell injury
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/10.1016/s1875-5364(25)60910-1openalex-snapshot
First-in-class drug oroxylin A tablets for treating hepatic and gastrointestinal disorders: from preclinical development to clinical research
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.orglett.3c02374openalex-snapshot
Influence of Ring Strain on the Formation of Rearrangement vs Cyclization Isotwistane Products in the Acyl Radical Reaction of Bicyclo[2.2.2]octanone
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/10.2139/ssrn.7519518openalex-snapshot
Anemarrhenones G and H, epimeric polycyclic benzophenones with a novel cage-like skeleton from the fibrous roots of Anemarrhena asphodeloides
inferred← citeshttps://doi.org/10.3389/fntpr.2022.1086897openalex-snapshot
Computational methods and points for attention in absolute configuration determination
inferred← citeshttps://doi.org/10.3390/compounds4020025openalex-snapshot
New Compounds from Terrestrial Plants: A Perspective View
inferred← citeshttps://doi.org/10.3390/plants11192509openalex-snapshot
Hypericum Genus as a Natural Source for Biologically Active Compounds
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.