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Discovery of Structurally Intriguing Hache Inhibitors from Tropic Rhodomyrtus Tomentosa Leaves: Isolation, Configuration Assignment, Hache Inhibitory Activities, and Molecular Docking Studies

https://doi.org/10.2139/ssrn.4848548
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Total Synthesis of Myrtucommulone A
inferredcites →https://doi.org/10.1002/anie.201814421openalex-extracted
Isolation and Synthesis of Novel Meroterpenoids from Rhodomyrtus tomentosa: Investigation of a Reactive Enetrione Intermediate
inferredcites →https://doi.org/10.1007/s11101-020-09697-2openalex-extracted
Phloroglucinols from Myrtaceae: attractive targets for structural characterization, biological properties and synthetic procedures
inferredcites →https://doi.org/10.1016/j.bioorg.2020.104127openalex-extracted
Acylphloroglucinols with acetylcholinesterase inhibitory effects from the fruits of Eucalyptus robusta
inferredcites →https://doi.org/10.1016/j.bioorg.2020.104519openalex-extracted
Polymethylated acylphloroglucinols from Rhodomyrtus tomentosa exert acetylcholinesterase inhibitory effects
inferredcites →https://doi.org/10.1016/j.bioorg.2021.105303openalex-extracted
Non-volatile acylphloroglucinol components from Eucalyptus robusta inhibit Zika virus by impairing RdRp activity of NS5
inferredcites →https://doi.org/10.1016/j.bioorg.2021.105404openalex-extracted
Acylphloroglucinol trimers from Callistemon salignus seeds: Isolation, configurational assignment, hAChE inhibitory effects, and molecular docking studies
inferredcites →https://doi.org/10.1016/j.bioorg.2023.106836openalex-extracted
Oligomeric phloroglucinols with hAChE inhibitory and antibacterial activities from tropic Rhodomyrtus tomentosa
inferredcites →https://doi.org/10.1016/j.bioorg.2024.107152openalex-extracted
A comprehensive review of multi-target directed ligands in the treatment of Alzheimer’s disease
inferredcites →https://doi.org/10.1016/j.bmcl.2017.03.065openalex-extracted
Antiplasmodial β-triketones from the flowers of the Australian tree Angophora woodsiana
inferredcites →https://doi.org/10.1016/j.phytochem.2022.113394openalex-extracted
Phloroglucinols with hAChE and α-glucosidase inhibitory activities from the leaves of tropic Rhodomyrtus tomentosa
inferredcites →https://doi.org/10.1016/j.phytol.2017.05.013openalex-extracted
Rhodomyrtosones G and H, minor phloroglucinols from the leaves of Rhodomyrtus tomentosa
inferredcites →https://doi.org/10.1016/j.tet.2008.09.054openalex-extracted
New acylphloroglucinols from the leaves of Rhodomyrtus tomentosa
inferredcites →https://doi.org/10.1016/j.tet.2017.01.052openalex-extracted
Acylphloroglucinol derivatives from the twigs and leaves of Callistemon salignus
inferredcites →https://doi.org/10.1021/acs.jafc.1c08089openalex-extracted
Six Unusual Meroterpenoids from the Leaves of Psidium guajava L. and Their PTP1B Inhibitory Activities
inferredcites →https://doi.org/10.1021/acs.jafc.7b01762openalex-extracted
Meroterpenoids with Antitumor Activities from Guava (Psidium guajava)
inferredcites →https://doi.org/10.1021/acs.jnatprod.3c00139openalex-extracted
NMR Fingerprints of Formyl Phloroglucinol Meroterpenoids and Their Application to the Investigation of Eucalyptus gittinsii subsp. gittinsii
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b01005openalex-extracted
Isolation, Structure Elucidation, and Absolute Configuration of Syncarpic Acid-Conjugated Terpenoids from Rhodomyrtus tomentosa
inferredcites →https://doi.org/10.1021/acs.jnatprod.8b00430openalex-extracted
Eucalypglobulusals A–J, Formyl-Phloroglucinol–Terpene Meroterpenoids from Eucalyptus globulus Fruits
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00064openalex-extracted
Callistemonols A and B, Potent Antimicrobial Acylphloroglucinol Derivatives with Unusual Carbon Skeletons from Callistemon viminalis
inferredcites →https://doi.org/10.1021/acs.joc.2c00071openalex-extracted
Discovery and Biomimetic Synthesis of a Polycyclic Polymethylated Phloroglucinol Collection from Rhodomyrtus tomentosa
inferredcites →https://doi.org/10.1021/acs.joc.5b01570openalex-extracted
Divergent Total Syntheses of Rhodomyrtosones A and B
inferredcites →https://doi.org/10.1021/acs.orglett.0c02943openalex-extracted
The Biomimetic Total Syntheses of the Antiplasmodial Tomentosones A and B
inferredcites →https://doi.org/10.1021/acs.orglett.1c01616openalex-extracted
Rhodomentosones A and B: Two Pairs of Enantiomeric Phloroglucinol Trimers from Rhodomyrtus tomentosa and Their Asymmetric Biomimetic Synthesis
inferredcites →https://doi.org/10.1021/acs.orglett.8b02259openalex-extracted
Eucalyptusdimers A–C, Dimeric Phloroglucinol–Phellandrene Meroterpenoids from Eucalyptus robusta
inferredcites →https://doi.org/10.1021/acs.orglett.9b00108openalex-extracted
Isolation, Structure Elucidation, and Total Synthesis of Myrtuspirone A from Myrtus communis
inferredcites →https://doi.org/10.1021/acs.orglett.9b03299openalex-extracted
Biomimetic Synthesis of Psiguajdianone Guided Discovery of the Meroterpenoids from Psidium guajava
inferredcites →https://doi.org/10.1021/jo201602yopenalex-extracted
Tomentosones A and B, Hexacyclic Phloroglucinol Derivatives from the Thai Shrub Rhodomyrtus tomentosa
inferredcites →https://doi.org/10.1021/ol302849vopenalex-extracted
Isolation and Biomimetic Synthesis of (±)-Guajadial B, a Novel Meroterpenoid from Psidium guajava
inferredcites →https://doi.org/10.1039/c2ob26931gopenalex-extracted
Watsonianone A–C, anti-plasmodial β-triketones from the Australian tree, Corymbia watsoniana
inferredcites →https://doi.org/10.1039/c8ob02687dopenalex-extracted
Meroterpene-like compounds derived from β-caryophyllene as potent α-glucosidase inhibitors
inferredcites →https://doi.org/10.1039/c8qo00130hopenalex-extracted
Asymmetric total syntheses of callistrilones B, G and J
inferredcites →https://doi.org/10.1039/d1qo00989copenalex-extracted
A biomimetic synthesis-enabled stereochemical assignment of rhodotomentones A and B, two unusual caryophyllene-derived meroterpenoids from Rhodomyrtus tomentosa
inferredcites →https://doi.org/10.1093/ijnp/pyy091openalex-extracted
Antidepressant Effects of Rhodomyrtone in Mice with Chronic Unpredictable Mild Stress-Induced Depression
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