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Lignans from the Fruit of Schisandra glaucescens with Antioxidant and Neuroprotective Properties
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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/cbdv.200900367openalex-snapshot
7,8‐Secolignans from Schisandra wilsoniana and Their Anti‐HIV‐1 Activities
inferredcites →https://doi.org/10.1002/hlca.201100033openalex-snapshot
Triterpenoids from the Stems of Schisandra glaucescens
inferredcites →https://doi.org/10.1002/jnr.20089openalex-snapshot
Dibenzocyclooctadiene lignans from Schisandra chinensis protect primary cultures of rat cortical cells from glutamate‐induced toxicity
inferredcites →https://doi.org/10.1002/ptr.3269openalex-snapshot
Protective effects of dibenzocyclooctadiene lignans from Schisandra chinensis against beta‐amyloid and homocysteine neurotoxicity in PC12 cells
inferredcites →https://doi.org/10.1016/0031-9422(90)85206-uopenalex-snapshot
Arylnaphthalene neolignans from Virola calophylla
inferredcites →https://doi.org/10.1016/j.fitote.2012.04.007openalex-snapshot
Cycloartane triterpenoids from the stems of Schisandra glaucescens and their bioactivity
inferredcites →https://doi.org/10.1016/j.fitote.2013.05.006openalex-snapshot
Neuroprotective compounds from the bulbs of Lycoris radiata
inferredcites →https://doi.org/10.1016/j.phytochem.2004.01.004openalex-snapshot
Aryltetralone lignans and 7,8-seco-lignans from Holostylis reniformis
inferredcites →https://doi.org/10.1016/j.phytochem.2007.05.003openalex-snapshot
Lignans, an amide and anti-platelet activities from Piper philippinum
inferredcites →https://doi.org/10.1016/j.phytol.2012.12.008openalex-snapshot
Lignans from the fruit of Schisandra sphenanthera, and their inhibition of HSV-2 and adenovirus
inferredcites →https://doi.org/10.1016/s0031-9422(00)83546-3openalex-snapshot
Lignans from Piper cubeba
inferredcites →https://doi.org/10.1016/s0031-9422(00)94440-6openalex-snapshot
Neolignans from Virola carinata☆
inferredcites →https://doi.org/10.1016/s0031-9422(99)00457-4openalex-snapshot
Two glycosides from the stem bark of Tetracentron sinense
inferredcites →https://doi.org/10.1016/s0040-4020(01)98893-3openalex-snapshot
New lignans from the heartwood of cleistanthus collinus
inferredcites →https://doi.org/10.1021/ci6005646openalex-snapshot
Generating Conformer Ensembles Using a Multiobjective Genetic Algorithm
inferredcites →https://doi.org/10.1021/cr9904009openalex-snapshot
Quantum Mechanical Continuum Solvation Models
inferredcites →https://doi.org/10.1021/np034002jopenalex-snapshot
New Bioactive Polyphenols fromTheobromagrandiflorum(“Cupuaçu”)
inferredcites →https://doi.org/10.1021/np100607sopenalex-snapshot
Microbial Transformations of Aryltetralone and Aryltetralin Lignans by Cunninghamella echinulata and Beauveria bassiana
inferredcites →https://doi.org/10.1021/np1009288openalex-snapshot
Dibenzocyclooctadiene Lignans with Antineurodegenerative Potential from Kadsura ananosma
inferredcites →https://doi.org/10.1021/np200937hopenalex-snapshot
Dibenzocyclooctadiene Lignans fromKadsura polyspermaand Their Antineurodegenerative Activities
inferredcites →https://doi.org/10.1021/ol200188nopenalex-snapshot
Schiglautone A, a New Tricyclic Triterpenoid with a Unique 6/7/9-Fused Skeleton from the Stems of Schisandra glaucescens
inferredcites →https://doi.org/10.1055/s-0029-1185537openalex-snapshot
Dibenzocyclooctadiene Lignans and Lanostane Derivatives from the Roots ofKadsura coccineaand their Protective Effects on Primary Rat Hepatocyte Injury Induced byt-Butyl Hydroperoxide
inferredcites →https://doi.org/10.1055/s-0031-1298214openalex-snapshot
Lanostane Triterpenoids from the Stems ofSchisandra glaucescens
inferredcites →https://doi.org/10.1055/s-0032-1327895openalex-snapshot
Neuroprotective Lignans from the Stems of Schisandra glaucescens
inferredcites →https://doi.org/10.1055/s-2005-916220openalex-snapshot
New Cytotoxic Tetrahydrofuran- and Dihydrofuran-Type Lignans from the Stem ofBeilschmiedia tsangii
inferredcites →https://doi.org/10.1080/10286020.2013.784277openalex-snapshot
Two new compounds fromSchisandra glaucescens
inferredcites →https://doi.org/10.1080/10286020.2013.824428openalex-snapshot
Four new lignans from Schisandra sphenanthera
inferredcites →https://doi.org/10.1139/v81-250openalex-snapshot
The structure of chicanine, a new lignan from Schisandra sp .
inferredcites →https://doi.org/10.1177/1934578x0900401123openalex-snapshot
Two New Lignans from the Fruits of Schisandra sphenanthera
inferredcites →https://doi.org/10.1248/cpb.35.501openalex-snapshot
Gas-liquid chromatographic separation of aldose enantiomers as trimethylsilyl ethers of methyl 2-(polyhydroxyalkyl)-thiazolidine-4(R)-carboxylates.
inferredcites →https://doi.org/10.1590/s0103-50532012005000054openalex-snapshot
7,8-secolignans from Schisandra neglecta and their anti-HIV-1 activities
inferredcites →https://doi.org/10.3892/etm.2014.1891openalex-snapshot
Effect of Fuzheng Huayu capsule combined with Pegasys on genotype 1 hepatitis C fibrosis and cell apoptosis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Diterpenoids from the Root Bark of Acanthopanax Gracilistylus and Their Inhibitory Effects on Neutrophil Elastase, Cyclooxygenase-1, and Cyclooxygenase-2 in Vitro
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inferred← citeshttps://doi.org/10.1016/j.bse.2021.104328openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fitote.2016.07.005openalex-snapshot
Triterpenoids from the fruit of Schisandra glaucescens
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105142openalex-snapshot
Lignans and sesquiterpenes from Schisandra tomentella A. C. Smith
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106021openalex-snapshot
Diterpenoids from Acanthopanacis Cortex and their anti-inflammatory activity studies
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106415openalex-snapshot
Schisandraceae family fruits: Exploring chemophenetic significance, UPLC/MSn database, phytochemistry, and pharmacological potential
inferred← citeshttps://doi.org/10.1016/j.foodchem.2022.132143openalex-snapshot
Why natural antioxidants are readily recognized by biological systems? 3D architecture plays a role!
inferred← citeshttps://doi.org/10.1016/j.indcrop.2017.08.053openalex-snapshot
Potential antioxidants for biodiesel from a softwood lignin pyrolyzate
inferred← citeshttps://doi.org/10.1016/j.jep.2015.02.009openalex-snapshot
Effects of Schisandra chinensis extracts on cough and pulmonary inflammation in a cough hypersensitivity guinea pig model induced by cigarette smoke exposure
inferred← citeshttps://doi.org/10.1016/j.jep.2016.11.011openalex-snapshot
Effects of the stem extracts of Schisandra glaucescens Diels on collagen-induced arthritis in Balb/c mice
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114208openalex-snapshot
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Anticancer activity of lignan compounds against breast cancer proteins (BRCA1 and BRCA2): A computational approach
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00292openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.1c01780openalex-snapshot
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Design, synthesis and anticancer activities of novel otobain derivatives
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Triflimide-catalyzed allylsilane annulations of benzylic alcohols for the divergent synthesis of indanes and tetralins
inferred← citeshttps://doi.org/10.1039/c7ra06322aopenalex-snapshot
Preparation, characterization and the adsorption characteristics of lignin/silica nanocomposites from cellulosic ethanol residue
inferred← citeshttps://doi.org/10.1055/a-1916-4510openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/10286020.2016.1234456openalex-snapshot
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