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Bioactive Asarone-Derived Phenylpropanoids from the Rhizome of Acorus tatarinowii Schott

https://doi.org/10.1021/acs.jnatprod.7b00457
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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/mrc.4393openalex-snapshot
Bioactive Nitrogenous Compounds from Acorus tatarinowii
inferredcites →https://doi.org/10.1002/ptr.5337openalex-snapshot
Anticonvulsant and Sedative Effects of Eudesmin isolated from Acorus tatarinowii on mice and rats
inferredcites →https://doi.org/10.1006/bbrc.1996.1637openalex-snapshot
6-Hydroxycatecholine, a Choline-Mimicking Analogue of the Selective Neurotoxin, 6-Hydroxydopamine
inferredcites →https://doi.org/10.1007/s12272-009-1303-1openalex-snapshot
Lignan constituents from Chloranthus japonicus Sieb.
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.bmcl.2015.08.001openalex-snapshot
A novel sesquiterpene and three new phenolic compounds from the rhizomes of Acorus tatarinowii Schott
inferredcites →https://doi.org/10.1016/j.carbpol.2015.07.018openalex-snapshot
Characterization of polysaccharides with antioxidant and immunological activities from Rhizoma Acori Tatarinowii
inferredcites →https://doi.org/10.1016/j.cclet.2016.06.051openalex-snapshot
A new bisbenzylisoquinoline alkaloid from Plumulanelumbinis
inferredcites →https://doi.org/10.1016/j.foodchem.2014.06.106openalex-snapshot
Extraction, chemical composition and antioxidant activity of flavonoids from Cyclocarya paliurus (Batal.) Iljinskaja leaves
inferredcites →https://doi.org/10.1016/j.foodchem.2016.07.105openalex-snapshot
Polyphenols from wolfberry and their bioactivities
inferredcites →https://doi.org/10.1016/j.neulet.2009.02.011openalex-snapshot
Neuroprotective effect of alpha-asarone on spatial memory and nitric oxide levels in rats injected with amyloid-β(25–35)
inferredcites →https://doi.org/10.1016/j.phymed.2013.09.020openalex-snapshot
An overview on traditional uses and pharmacological profile of Acorus calamus Linn. (Sweet flag) and other Acorus species
inferredcites →https://doi.org/10.1016/j.phymed.2017.04.003openalex-snapshot
Pharmacology and toxicology of α- and β-Asarone: A review of preclinical evidence
inferredcites →https://doi.org/10.1016/j.tetlet.2012.10.104openalex-snapshot
Syntheses of (−)-Tatarinoid A, (±)-Tatarinoid B, and (−)-Tatarinoid C
inferredcites →https://doi.org/10.1016/s0031-9422(98)00362-8openalex-snapshot
Glochidioboside, a glucoside of (7S,8R)-dihydrodehydrodiconiferyl alcohol from leaves of glochidion obovatum
inferredcites →https://doi.org/10.1016/s0367-326x(00)00240-9openalex-snapshot
Lignans from Strophanthus gratus
inferredcites →https://doi.org/10.1021/acs.jafc.6b01909openalex-snapshot
Antidiabetic Potential of Purple and Red Rice ( Oryza sativa L.) Bran Extracts
inferredcites →https://doi.org/10.1021/cr2003344openalex-snapshot
Assignment of the Absolute Configuration of Polyfunctional Compounds by NMR Using Chiral Derivatizing Agents
inferredcites →https://doi.org/10.1021/jo1022712openalex-snapshot
Glucokinase-Activating Sesquinlignans from the Rhizomes of Acorus tatarinowii Schott
inferredcites →https://doi.org/10.1021/jo961607uopenalex-snapshot
Intramolecular Regioselective Insertion into Unactivated Prochiral Carbon−Hydrogen Bonds with Diazoacetates of Primary Alcohols Catalyzed by Chiral Dirhodium(II) Carboxamidates. Highly Enantioselective Total Synthesis of Natural Lignan Lactones
inferredcites →https://doi.org/10.1021/np300417qopenalex-snapshot
α-Glucosidase Inhibitory Hydrolyzable Tannins from Eugenia jambolana Seeds
inferredcites →https://doi.org/10.1021/np900793eopenalex-snapshot
Compounds from Acorus tatarinowii: Determination of Absolute Configuration by Quantum Computations and cAMP Regulation Activity
inferredcites →https://doi.org/10.1021/ol100451popenalex-snapshot
Acortatarins A and B, Two Novel Antioxidative Spiroalkaloids with a Naturally Unusual Morpholine Motif from Acorus tatarinowii
inferredcites →https://doi.org/10.1038/srep22909openalex-snapshot
Antioxidant Lignans and Neolignans from Acorus tatarinowii
inferredcites →https://doi.org/10.1039/c4ra06481jopenalex-snapshot
New sesquiterpenoids from the rhizomes of Acorus tatarinowii
inferredcites →https://doi.org/10.1039/c4ra12049copenalex-snapshot
Acorus Linnaeus: a review of traditional uses, phytochemistry and neuropharmacology
inferredcites →https://doi.org/10.1039/c6ra27786aopenalex-snapshot
Anti-neuroinflammatory asarone derivatives from the rhizomes of Acorus tatarinowii
inferredcites →https://doi.org/10.1055/s-2000-8628openalex-snapshot
Phenylpropanes fromAcorus tatarinowii
inferredcites →https://doi.org/10.1080/10286020.2010.490522openalex-snapshot
Alkaloids and sesquiterpenoids fromAcorus tatarinowii
inferredcites →https://doi.org/10.1093/mutage/gew007openalex-snapshot
Comparative investigation of the mutagenicity of propenylic and allylic asarone isomers in the Ames fluctuation assay
inferredcites →https://doi.org/10.1111/j.0013-9580.2005.461007.xopenalex-snapshot
Study of Antiepileptic Effect of Extracts from Acorus tatarinowii Schott
inferredcites →https://doi.org/10.1248/cpb.41.772openalex-snapshot
Chalcones as Synthetic Intermediates. A Facile Route to (.+-.)-Magnosalicin, an Antiallergy Neolignan.
inferredcites →https://doi.org/10.3923/ajps.2011.182.189openalex-snapshot
An Update on Chemical Composition and Bioactivities of Acorus Species

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.2022.113143zenodo-depositor-declared
Liglaurates A–E, cytotoxic bis(lauric acid-12yl)lignanoates from the rhizomes of Drynaria roosii Nakaike
inferred← citeshttps://doi.org/10.1002/cbdv.202100252openalex-snapshot
Dimeric Acylphloroglucinol Derivatives with New Skeletons from Leptospermum scoparium
inferred← citeshttps://doi.org/10.1002/cbin.11197openalex-snapshot
Tatarinan T, an α‐asarone‐derived lignin, attenuates osteoclastogenesis induced by RANKL via the inhibition of NFATc1/c‐Fos expression
inferred← citeshttps://doi.org/10.1007/s10600-023-04087-4openalex-snapshot
Two New Biphenylpropanoids from the Rhizomes of Acorus tatarinowii
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105307openalex-snapshot
Bioactive phenylpropanoid derivatives from the fruits of Lycium ruthenicum Murr
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111609openalex-snapshot
Potential therapeutic natural products against Alzheimer's disease with Reference of Acetylcholinesterase
inferred← citeshttps://doi.org/10.1016/j.cej.2025.166385openalex-snapshot
Sustainable extraction and enrichment of natural phenylpropanoids with anti-glioma activities from Acorus gramineus
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104184openalex-snapshot
New phthalide derivatives from the Biscogniauxia sp. and their activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104189openalex-snapshot
Lignans from Isatis indigotica roots and their inhibitory effects on nitric oxide production
inferred← citeshttps://doi.org/10.1016/j.jplph.2023.154098openalex-snapshot
Functional analysis of a dirigent protein AtsDIR23 in Acorus tatarinowii
inferred← citeshttps://doi.org/10.1016/j.phrs.2019.104284openalex-snapshot
Lignans and Neolignans: Plant secondary metabolites as a reservoir of biologically active substances
inferred← citeshttps://doi.org/10.1016/j.phyplu.2021.100184openalex-snapshot
Advances on plant extracts and phytocompounds with acetylcholinesterase inhibition activity for possible treatment of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.phytochem.2019.112212openalex-snapshot
The asarone-derived phenylpropanoids from the rhizome of Acorus calamus var. angustatus Besser
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113626openalex-snapshot
Acorus calamus var. angustatus Besser: Insight into current research on ethnopharmacological use, phytochemistry, pharmacology, toxicology, and pharmacokinetics
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.03.008openalex-snapshot
Four anti-inflammatory aromadendrane sesquiterpenoid fucosides and other constituents from Pittosporum glabratum var. neriifolium
inferred← citeshttps://doi.org/10.1016/s1875-5364(21)60088-2openalex-snapshot
Biotransformation of α-asarone by Alternaria longipes CGMCC 3.2875
inferred← citeshttps://doi.org/10.1016/s1875-5364(24)60629-1openalex-snapshot
New pimarane diterpenoids with antibacterial activity from fungus Arthrinium sp. ZS03
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c05513openalex-snapshot
Quantitative Analysis of β-Asarone Derivatives in Acorus calamus and Herbal Food Products by HPLC-MS/MS
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c01998openalex-snapshot
Syntheses of Tetrahydropyran Type 8,7′-Neolignans Using a Ring-Expansion Reaction and Tetrahydrofuran Type 8,7′-Neolignans to Discover a Novel Phytotoxic Neolignan
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00356openalex-snapshot
Syntheses of Anti-Phytopathogenic Fungal 2,7′-Cyclo-7,8′-neolignan-Type Indanes and Preparation of 8′-Epimer
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00208openalex-snapshot
Enantiomeric Prenylated Neolignans from the Roots of Illicium verum with Analgesic Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00461openalex-snapshot
Colocynthenins A–D, Ring-A seco-Cucurbitane Triterpenoids from the Fruits of Citrullus colocynthis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00287openalex-snapshot
Structure-Based Molecular Networking for the Target Discovery of Oxahomoaporphine and 8-Oxohomoaporphine Alkaloids from Duguetia surinamensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00471openalex-snapshot
Cinerols, Nitrogenous Meroterpenoids from the Marine Sponge Dysidea cinerea
inferred← citeshttps://doi.org/10.1021/jacs.6c17816openalex-snapshot
Asymmetric Transfer Hydrogenation of Acyclic 1,4-Diketones for the Synthesis of Diversified Cyclic Products via Double Dynamic Kinetic Resolution
inferred← citeshttps://doi.org/10.1039/d1ob00008jopenalex-snapshot
Stereocontrolled syntheses of (−)- and (+)-γ-diisoeugenol along with optically active eight stereoisomers of 7,8′-epoxy-8,7′-neolignan
inferred← citeshttps://doi.org/10.1039/d6ra02514eopenalex-snapshot
Synthesis, characterization, and α-glucosidase inhibitory activity of methyl proline derivatives of phenylpropanoid
inferred← citeshttps://doi.org/10.1080/07060661.2026.2635443openalex-snapshot
First report of an Acorus tatarinowii leaf blight caused by Pestalotiopsis microspora in China
inferred← citeshttps://doi.org/10.1080/14786419.2022.2038595openalex-snapshot
Two new diterpenoids from the rhizomes of Zingiber officinale
inferred← citeshttps://doi.org/10.1080/14786419.2023.2216348openalex-snapshot
One undescribed glycoside benzofuran derivative and a new p -hydroxybenzoate glycoside from the leaves of Illicium dunnianum Tutcher
inferred← citeshttps://doi.org/10.1080/14786419.2023.2290684openalex-snapshot
Four new constituents from the fruits of Cyclocodon lancifolius (Roxburgh) Kurz
inferred← citeshttps://doi.org/10.1097/md.0000000000021674openalex-snapshot
Nonsurgical treatment of chronic subdural hematoma with Chinese herbal medicine
inferred← citeshttps://doi.org/10.1186/s13321-026-01192-8openalex-snapshot
Is scaffold hopping possible in machine learning using the electronic-structure-informatics (ESI) descriptor set? an application to natural-product-based drug discovery of α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.18311/jeoh/2022/29511openalex-snapshot
Therapeutic Efficacy of Natural Phytochemicals as Acetylcholinesterase Inhibitors Against Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fphar.2020.00397openalex-snapshot
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes
inferred← citeshttps://doi.org/10.3390/app122111007openalex-snapshot
Ultrasound-Assisted Extraction of β-Asarone from Sweet Flag (Acorus calamus) Rhizome
inferred← citeshttps://doi.org/10.3390/d15020176openalex-snapshot
The First Genome from the Basal Monocot Family Has Been Misnamed: Taxonomic Identity of Acorus tatarinowii (Acoraceae), a Source of Numerous Chemical Compounds of Pharmaceutical Importance
inferred← citeshttps://doi.org/10.3390/jcm9041176openalex-snapshot
Role of Vacha (Acorus calamus Linn.) in Neurological and Metabolic Disorders: Evidence from Ethnopharmacology, Phytochemistry, Pharmacology and Clinical Study
inferred← citeshttps://doi.org/10.3390/jox15050156openalex-snapshot
Phytochemical Profile and Acute Toxicity in CD-1 Mice of the Hydroethanolic Extract and Butanolic Fraction of Piper marginatum Jacq.
inferred← citeshttps://doi.org/10.3390/md19080416openalex-snapshot
New Drimane Sesquiterpenes and Polyketides from Marine-Derived Fungus Penicillium sp. TW58-16 and Their Anti-Inflammatory and α-Glucosidase Inhibitory Effects
inferred← citeshttps://doi.org/10.3390/molecules27041279openalex-snapshot
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties
inferred← citeshttps://doi.org/10.3390/molecules27134113openalex-snapshot
Comprehensive Phytochemical Profiling, Biological Activities, and Molecular Docking Studies of Pleurospermum candollei: An Insight into Potential for Natural Products Development
inferred← citeshttps://doi.org/10.3390/molecules28114525openalex-snapshot
Acorus tatarinowii Schott: A Review of Its Botany, Traditional Uses, Phytochemistry, and Pharmacology
inferred← citeshttps://doi.org/10.3390/molecules28207117openalex-snapshot
Ethnic, Botanic, Phytochemistry and Pharmacology of the Acorus L. Genus: A Review
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