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Bioactive Lignans from the Trunk of Abies holophylla
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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.1780openalex-snapshot
Lignans from the bark extract of Pinus sylvestris L.
inferredcites →https://doi.org/10.1002/omr.1270210208openalex-snapshot
13C NMR spectral analysis of dihydrobenzofuran lignans
inferredcites →https://doi.org/10.1007/s11094-007-0019-0openalex-snapshot
Antioxidant activity of polyphenols from the far-east plant Taxus cuspidata
inferredcites →https://doi.org/10.1007/s12272-011-1206-9openalex-snapshot
A new lignan glycoside from Juniperus rigida
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/0031-9422(82)80172-6openalex-snapshot
Two lignans from Cedrus deodara
inferredcites →https://doi.org/10.1016/j.bmcl.2011.02.003openalex-snapshot
Furostanol saponins from the rhizomes of Dioscorea japonica and their effects on NGF induction
inferredcites →https://doi.org/10.1016/j.bse.2003.07.004openalex-snapshot
3-O-Methylrhamnose in lower land plant primary cell walls
inferredcites →https://doi.org/10.1016/j.orggeochem.2007.02.005openalex-snapshot
Characterization of methyl sugars, 3-deoxysugars and methyl deoxysugars in marine high molecular weight dissolved organic matter
inferredcites →https://doi.org/10.1016/j.phytochem.2003.10.025openalex-snapshot
Neolignan and flavonoid glycosides in Juniperus communis var. depressa
inferredcites →https://doi.org/10.1016/j.phytochem.2006.01.019openalex-snapshot
Configurational analysis of cubebins and bicubebin from Aristolochia lagesiana and Aristolochia pubescens
inferredcites →https://doi.org/10.1016/j.phytochem.2011.11.011openalex-snapshot
Sesquiterpenoids and triterpenoids from Abies holophylla and their bioactivities
inferredcites →https://doi.org/10.1016/j.phytochem.2012.07.013openalex-snapshot
Terpene and lignan glycosides from the twigs and leaves of an endangered conifer, Cathaya argyrophylla
inferredcites →https://doi.org/10.1016/j.phytol.2012.04.002openalex-snapshot
Two new compounds from Abies holophylla
inferredcites →https://doi.org/10.1017/cbo9780511983665.009openalex-snapshot
Determination of structure
inferredcites →https://doi.org/10.1021/jf048945dopenalex-snapshot
Bioactive Lignans from a Cultivar of Helianthus annuus
inferredcites →https://doi.org/10.1021/jf061694jopenalex-snapshot
New Lignans from the Perisperm of Sesamum indicum
inferredcites →https://doi.org/10.1021/jo960719iopenalex-snapshot
MTPA vs MPA in the Determination of the Absolute Configuration of Chiral Alcohols by 1H NMR
inferredcites →https://doi.org/10.1021/np050089sopenalex-snapshot
Effect of Benzylic Oxygen on the Antioxidant Activity of Phenolic Lignans
inferredcites →https://doi.org/10.1021/np1005357openalex-snapshot
Caffeic Acid Esters and Lignans from Piper sanguineispicum
inferredcites →https://doi.org/10.1021/np200541mopenalex-snapshot
Bioactive Lignans from the Rhizomes of Acorus gramineus
inferredcites →https://doi.org/10.1021/np900443qopenalex-snapshot
Steroidal Saponins from Chlorophytum orchidastrum
inferredcites →https://doi.org/10.1055/s-0030-1250122openalex-snapshot
Two New Lignans from the Roots ofPulsatilla koreana
inferredcites →https://doi.org/10.1055/s-0031-1280020openalex-snapshot
Antimicrobial, Cytotoxic Lignans and Terpenoids from the Twigs ofPseudolarix kaempferi
inferredcites →https://doi.org/10.1071/ch9851631openalex-snapshot
Chemistry of the Podocarpaceae. LXIX. Further Lignans from te Wood of Dacrydium intermedium
inferredcites →https://doi.org/10.1246/cl.1995.513openalex-snapshot
Application of Modified Mosher’s Method to α-Aromatic Secondary Alcohols. Exception of the Rule and Conformational Analyses
inferredcites →https://doi.org/10.1248/cpb.44.1122openalex-snapshot
Studies on the Constiuents of Viburnum Species. Part XIII. Isolation and Absolute Structures of the Neolignan Glycosides with the Enantiometric Aglycones from the Leaves of Viburnum awabuki K. KOCH.
inferredcites →https://doi.org/10.1248/cpb.50.669openalex-snapshot
A New Lignan Glycoside from the Leaves of Sambucus sieboldiana (Miq.) Blume ex. Graebn.
inferredcites →https://doi.org/10.1515/hf.2005.067openalex-snapshot
Bioactive phenolic substances in industrially important tree species. Part 4: Identification of two new 7-hydroxy divanillyl butyrolactol lignans in some spruce, fir, and pine species
inferredcites →https://doi.org/10.1515/znb-2011-0715openalex-snapshot
Benzoic Acid Allopyranosides and Lignan Glycosides from the Twigs of Keteleeria evelyniana
inferredcites →https://doi.org/10.4014/jmb.0811.630openalex-snapshot
Comparative Analysis of Chemical Compositions and Antimicrobial Activities of Essential Oils from Abies holophylla and Abies koreana
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.2021.112962zenodo-depositor-declared
Glycosylated constituents isolated from the trunk of Abies holophylla and their anti-inflammatory and neurotrophic activity
inferred← citeshttps://doi.org/10.1002/cbdv.71650openalex-snapshot
Constituents From the Flowers of Viburnum macrocephalum f. macrocephalum and Their α ‐Amylase and α ‐Glucosidase Inhibitory Activities
inferred← citeshttps://doi.org/10.1002/cssc.202201875openalex-snapshot
Lignin Stabilization and Carbohydrate Nature in H‐transfer Reductive Catalytic Fractionation: The Role of Solvent Fractionation of Lignin Oil in Structural Profiling**
inferred← citeshttps://doi.org/10.1002/iub.2369openalex-snapshot
Boosting the autophagy‐lysosomal pathway by phytochemicals: A potential therapeutic strategy against Alzheimer's disease
inferred← citeshttps://doi.org/10.1007/978-981-13-1453-7_12openalex-snapshot
Neuroprotective Potential of Small Molecule Phytochemicals in Stroke Therapy
inferred← citeshttps://doi.org/10.1007/978-981-16-8158-5_17openalex-snapshot
Preventive Role and Mechanism of Herbal Medicine in Alzheimer’s Disease with Special Reference to Phenolic Compounds
inferred← citeshttps://doi.org/10.1007/s10600-023-03933-9openalex-snapshot
Chemical Constituents of Iberis amara Seeds
inferred← citeshttps://doi.org/10.1007/s11745-016-4172-7openalex-snapshot
Neuroprotective Fatty Acids from the Stem Bark of Sorbus commixta
inferred← citeshttps://doi.org/10.1007/s12272-014-0468-4openalex-snapshot
Isolation of a dihydrobenzofuran lignan, icariside E4, with an antinociceptive effect from Tabebuia roseo-alba (Ridley) Sandwith (Bignoniaceae) bark
inferred← citeshttps://doi.org/10.1016/j.bbii.2024.100048openalex-snapshot
Natural products as potential modulators of pro-inflammatory cytokines signalling in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.11.041openalex-snapshot
Phenylpropanoids and lignans from Prunus tomentosa seeds as efficient β-amyloid (Aβ) aggregation inhibitors
inferred← citeshttps://doi.org/10.1016/j.bse.2017.12.004openalex-snapshot
Chemical constituents from Tsuga longibracteata and its chemotaxonomic study
inferred← citeshttps://doi.org/10.1016/j.bse.2019.01.004openalex-snapshot
Sesquiterpenoids and lignans from the fruits of Illicium simonsii Maxim
inferred← citeshttps://doi.org/10.1016/j.cbi.2015.07.008openalex-snapshot
Kinetics and molecular docking studies of cholinesterase inhibitors derived from water layer of Lycopodiella cernua (L.) Pic. Serm. (II)
inferred← citeshttps://doi.org/10.1016/j.ejphar.2020.173651openalex-snapshot
α-Conidendrin inhibits the expression of intercellular adhesion molecule-1 induced by tumor necrosis factor-α in human lung adenocarcinoma A549 cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2015.03.011openalex-snapshot
Lignans from the root of Paeonia lactiflora and their anti-β-amyloid aggregation activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105664openalex-snapshot
Neurotrophic neolignans of Pinus koraiensis twigs
inferred← citeshttps://doi.org/10.1016/j.foodchem.2015.08.091openalex-snapshot
Phenolics from strawberry cv. Falandi and their antioxidant and α-glucosidase inhibitory activities
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.114601openalex-snapshot
Lignans with α-glucosidase, protein tyrosine phosphatase 1B, and aldose reductase inhibitory activities from the fruits of Viburnum cylindricum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114259openalex-snapshot
Major specialized natural products from the endangered plant Heptacodium miconioides, potential medicinal uses and insights into its longstanding unresolved systematic classification
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114798openalex-snapshot
Glycosidic phenylpropanoid dimers and trimers from Castanopsis choboensis and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2017.05.009openalex-snapshot
A new δ-tocotrienolic acid derivative and other constituents from the cones of Cedrus atlantica and their in vitro antimicrobial activity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.10.030openalex-snapshot
Holophyllin A, a rearranged abietane-type diterpenoid from the trunk of Abies holophylla
inferred← citeshttps://doi.org/10.1016/s1875-5364(21)60048-1openalex-snapshot
New oligomeric neolignans from the leaves of Magnolia officinalis var. biloba
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01053openalex-snapshot
Diterpenes from the Trunk of Abies holophylla and Their Potential Neuroprotective and Anti-inflammatory Activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00582openalex-snapshot
Wasabisides A–E, Lignan Glycosides from the Roots of Wasabia japonica
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b01124openalex-snapshot
Derivatives of the Lignan 7′-Hydroxymatairesinol with Antioxidant Properties and Enhanced Lipophilicity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00245openalex-snapshot
Structural Characterization of Terpenoids from Abies holophylla Using Computational and Statistical Methods and Their Biological Activities
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02184openalex-snapshot
Honolignols A–C, Three Racemic Forms of Honokiol-Derived Dimeric Neolignans from Magnolia Officinalis Var. Biloba
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03159openalex-snapshot
Stereoselective Total Synthesis of Formosanol, Tsugacetal, and Methyl β-Conidendral
inferred← citeshttps://doi.org/10.1021/np500488vopenalex-snapshot
Phenolic Glycosides from the Twigs of Salix glandulosa
inferred← citeshttps://doi.org/10.1038/s41598-024-78823-3openalex-snapshot
NO classifier prediction of anti neuroinflammatory agents using text mining of 3D molecular fingerprints
inferred← citeshttps://doi.org/10.1038/srep43646openalex-snapshot
Holophyllane A: A Triterpenoid Possessing an Unprecedented B-nor-3,4-seco-17,14-friedo-lanostane Architecture from Abies holophylla
inferred← citeshttps://doi.org/10.1039/c6np00021eopenalex-snapshot
Recent advances in research on lignans and neolignans
inferred← citeshttps://doi.org/10.1039/d5fd00109aopenalex-snapshot
Mass-resolved UV–Vis–GPC mapping diagnoses catalyst ageing in RCF lignin streams
inferred← citeshttps://doi.org/10.1155/2015/814068openalex-snapshot
Phytochemicals That Regulate Neurodegenerative Disease by Targeting Neurotrophins: A Comprehensive Review
inferred← citeshttps://doi.org/10.3389/fphar.2018.00548openalex-snapshot
Anti-neuroinflammatory Potential of Natural Products in Attenuation of Alzheimer's Disease
inferred← citeshttps://doi.org/10.3390/ijms22020965openalex-snapshot
Terpenoids from Abies holophylla Attenuate LPS-Induced Neuroinflammation in Microglial Cells by Suppressing the JNK-Related Signaling Pathway
inferred← citeshttps://doi.org/10.3746/jkfn.2020.49.6.569openalex-snapshot
Antioxidant and Anti-Inflammatory Effects of Abies holophylla Leaf Extract in LPS-Induced RAW 264.7 Cells
inferred← citeshttps://doi.org/10.3987/com-14-13035openalex-snapshot
A New Cyclic Triterpene Saponin from Phyteuma japonicum
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