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Prenylated Acylphloroglucinols and Meroterpenoids from Hypericum Plants

https://doi.org/10.3987/rev-14-sr(k)1
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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/anie.200701552openalex-snapshot
Total Synthesis and Revised Structure of Biyouyanagin A
inferredcites →https://doi.org/10.1002/anie.200902908openalex-snapshot
Construction of Two Vicinal Quaternary Carbons by Asymmetric Allylic Alkylation: Total Synthesis of Hyperolactone C and (−)‐Biyouyanagin A
inferredcites →https://doi.org/10.1002/anie.201103873openalex-snapshot
The Chemistry of the Polycyclic Polyprenylated Acylphloroglucinols
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/cbdv.200900247openalex-snapshot
Prenylated Benzophenone Peroxide Derivatives from Hypericum sampsonii
inferredcites →https://doi.org/10.1002/cbdv.201100154openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols and Cytotoxic Constituents of Hypericum androsaemum
inferredcites →https://doi.org/10.1002/chem.201001474openalex-snapshot
Total Synthesis and Structural Revision of Biyouyanagin B
inferredcites →https://doi.org/10.1002/chem.201101082openalex-snapshot
Synthesis of the Anti‐HIV Agent (−)‐Hyperolactone C by Using Oxonium Ylide Formation–Rearrangement
inferredcites →https://doi.org/10.1002/jhet.5570380124openalex-snapshot
Synthesis of hyperolactones A and C
inferredcites →https://doi.org/10.1007/s13659-013-0032-9openalex-snapshot
Hypercohones A–C, acylphloroglucinol derivatives with homo-adamantane cores from Hypericum cohaerens
inferredcites →https://doi.org/10.1016/0031-9422(94)00862-nopenalex-snapshot
Spiro-lactones, hyperolactone A-D from Hypericum chinense
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.fitote.2012.08.022openalex-snapshot
Prenylated phloroglucinol derivatives from Hypericum sampsonii
inferredcites →https://doi.org/10.1016/j.lfs.2005.12.027openalex-snapshot
Hyperforin: More than an antidepressant bioactive compound?
inferredcites →https://doi.org/10.1016/j.phytochem.2005.04.024openalex-snapshot
An anti-staphylococcal acylphloroglucinol from Hypericum foliosum
inferredcites →https://doi.org/10.1016/j.phytochem.2006.08.017openalex-snapshot
Hyperforin
inferredcites →https://doi.org/10.1016/j.phytochem.2007.02.029openalex-snapshot
Sinaicinone, a complex adamantanyl derivative from Hypericum sinaicum
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.2011.01.032openalex-snapshot
Acylphloroglucinol and xanthones from Hypericum ellipticum
inferredcites →https://doi.org/10.1016/j.phytochem.2011.11.014openalex-snapshot
Phloroglucinol derivatives from Hypericum empetrifolium with antiproliferative activity on endothelial cells
inferredcites →https://doi.org/10.1016/j.phytol.2011.09.009openalex-snapshot
Four geranyl-bearing polyisoprenylated benzoylphloroglucinol derivatives from Hypericum sampsonii
inferredcites →https://doi.org/10.1016/j.tet.2011.06.079openalex-snapshot
Synthetic efforts toward [3.3.1] bridged bicyclic phloroglucinol natural products
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.2008.02.121openalex-snapshot
Takaneones A–C, prenylated butylphloroglucinol derivatives from Hypericum sikokumontanum
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/10.1016/j.tetlet.2012.01.052openalex-snapshot
Biyoulactones D and E, meroterpenoids from Hypericum chinense
inferredcites →https://doi.org/10.1016/s0040-4039(97)10713-4openalex-snapshot
Synthesis and absolute configuration of (+)-hyperolactone B
inferredcites →https://doi.org/10.1021/cr0500582openalex-snapshot
Polycyclic Polyprenylated Acylphloroglucinols
inferredcites →https://doi.org/10.1021/ja802805copenalex-snapshot
Total Synthesis, Revised Structure, and Biological Evaluation of Biyouyanagin A and Analogues Thereof
inferredcites →https://doi.org/10.1021/jo102511xopenalex-snapshot
Biomimetic Synthesis of Hyperolactones
inferredcites →https://doi.org/10.1021/np040149eopenalex-snapshot
Benzophenones from Hypericum carinatum
inferredcites →https://doi.org/10.1021/np0498962openalex-snapshot
A Direct Synthesis of Hyperolactone C
inferredcites →https://doi.org/10.1021/np0704147openalex-snapshot
Polyisoprenylated Benzoylphloroglucinol Derivatives from Hypericum sampsonii
inferredcites →https://doi.org/10.1021/np1004483openalex-snapshot
Norlignans, Acylphloroglucinols, and a Dimeric Xanthone from Hypericum chinense
inferredcites →https://doi.org/10.1021/np2003319openalex-snapshot
Antibacterial Acylphloroglucinols from Hypericum olympicum
inferredcites →https://doi.org/10.1021/np200741xopenalex-snapshot
Prenylated Acylphloroglucinols, Chipericumins A–D, from Hypericum chinense
inferredcites →https://doi.org/10.1021/np300237nopenalex-snapshot
Bi-, Tri-, and Polycyclic Acylphloroglucinols from Hypericum empetrifolium
inferredcites →https://doi.org/10.1021/np400287ropenalex-snapshot
Bioactive Polyprenylated Acylphloroglucinol Derivatives from Hypericum cohaerens
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/10.1021/ol050960wopenalex-snapshot
Biyouyanagin A, an Anti-HIV Agent from Hypericum chinense L. var. salicifolium
inferredcites →https://doi.org/10.1021/ol2021548openalex-snapshot
Biyoulactones A–C, New Pentacyclic Meroterpenoids from Hypericum chinense
inferredcites →https://doi.org/10.1021/ol403374hopenalex-snapshot
Bioinspired Total Synthesis of (±)-Yezo’otogirin C
inferredcites →https://doi.org/10.1021/ol802334yopenalex-snapshot
Consecutive Alkene Cross-Metathesis/Oxonium Ylide Formation−Rearrangement: Synthesis of the Anti-HIV Agent Hyperolactone C
inferredcites →https://doi.org/10.1039/a704159dopenalex-snapshot
First total synthesis of (±)-hyperolactone A
inferredcites →https://doi.org/10.1039/b600518gopenalex-snapshot
Phloroglucinol compounds of natural origin
inferredcites →https://doi.org/10.1039/b914364popenalex-snapshot
Phloroglucinol compounds of natural origin: Synthetic aspects
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/10.1073/pnas.1015258108openalex-snapshot
Design, synthesis, and biological evaluation of a biyouyanagin compound library
inferredcites →https://doi.org/10.1080/10286020.2012.680445openalex-snapshot
Three new phloroglucinol derivatives fromHypericum scabrum
inferredcites →https://doi.org/10.1080/14786419.2010.524647openalex-snapshot
Elegaphenone and 7-epi-clusianone, the major cytotoxic constituents ofHypericum elegans
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/10.1246/cl.2009.440openalex-snapshot
Geranyl Bearing Polyisoprenylated Benzoylphloroglucinol Derivatives from Hypericum sampsonii
inferredcites →https://doi.org/10.1248/cpb.58.336openalex-snapshot
Polyprenylated Benzoylphloroglucinol-Type Derivatives Including Novel Cage Compounds from Hypericum erectum
inferredcites →https://doi.org/10.1248/cpb.59.1250openalex-snapshot
Spirocyclic Acylphloroglucinol Derivatives from Hypericum beanii
inferredcites →https://doi.org/10.2165/00003088-200645050-00002openalex-snapshot
Hypericum Perforatum: A ???Modern??? Herbal Antidepressant

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.2021.112779zenodo-depositor-declared
(±)-hyperzewalsins A−D, four pairs of nor-monocyclic polyprenylated acylphloroglucinols with immunosuppressive activity from hypericum przewalskii maxim
inferred← citeshttps://doi.org/10.1002/chin.201511319openalex-snapshot
ChemInform Abstract: Prenylated Acylphloroglucinols and Meroterpenoids from Hypericum Plants
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/s11418-014-0853-9openalex-snapshot
Hypelodins A and B, polyprenylated benzophenones from Hypericum elodeoides
inferred← citeshttps://doi.org/10.1007/s11418-019-01350-3openalex-snapshot
Prenylated benzophenone derivatives from Hypericum patulum
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/s11418-021-01540-yopenalex-snapshot
Hyperdioxanes, dibenzo-1,4-dioxane derivatives from the roots of Hypericum ascyron
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105246openalex-snapshot
Discovery of bioactive polycyclic polyprenylated acylphloroglucinols from Hypericum wilsonii
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.08.014openalex-snapshot
Erecricins A–E, prenylated acylphloroglucinols from the roots of Hypericum erectum
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104363openalex-snapshot
Hypericum species: An analysis on the patent technologies
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.tet.2017.11.044openalex-snapshot
Phloroglucinol derivatives and a chromone glucoside from the leaves of Myrtus communis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.06.028openalex-snapshot
Merohyperins A–C, meroterpenes from the leaves of 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/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.8b01006openalex-snapshot
Prenylated Acylphloroglucinols from Hypericum faberi
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.6b02725openalex-snapshot
Hypatulins A and B, Meroterpenes from Hypericum patulum
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03594openalex-snapshot
gem-Diprenylation of Acylphloroglucinols by a Fungal Prenyltransferase of the Dimethylallyltryptophan Synthase Superfamily
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02739openalex-snapshot
Hyperdioxane A, a Conjugate of Dibenzo-1,4-dioxane and Sesquiterpene from Hypericum ascyron
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c07036openalex-snapshot
Organic–Inorganic Hybrid Nanoparticles Synthesized with Hypericum perforatum Extract: Potential Agents for Photodynamic Therapy at Ultra-low Power Light
inferred← citeshttps://doi.org/10.1021/np500827hopenalex-snapshot
Prenylated Benzophenones from Triadenum japonicum
inferred← citeshttps://doi.org/10.1039/d2ob00562jopenalex-snapshot
(±)-Walskiiglucinol A, a pair of rearranged acylphloroglucinol derivative enantiomers from Hypericum przewalskii
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/10.3390/molecules23123232openalex-snapshot
Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives
inferred← citeshttps://doi.org/10.3390/molecules27041279openalex-snapshot
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties
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