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Antioxidant and Anti-inflammatory Active Dihydrobenzofuran Neolignans from the Seeds of Prunus tomentosa

https://doi.org/10.1021/jf502171z
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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.200800022openalex-snapshot
Tarennanosides A–H, Eight New Lignan Glucosides from Tarenna attenuata and Their Protective Effect on H2O2‐Induced Impairment in PC12 Cells
inferredcites →https://doi.org/10.1002/hlca.201000116openalex-snapshot
Neolignans and Caffeoyl Derivatives from Selaginella moellendorffii
inferredcites →https://doi.org/10.1007/bf01053993openalex-snapshot
Lignin degradation byPhanerochaete chrysosporium: Metabolism of a phenolic phenylcoumaran substructure model compound
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Saponins in Tribulus terrestris – Chemistry and Bioactivity
inferredcites →https://doi.org/10.1007/s11418-007-0182-3openalex-snapshot
Lignan glycosides and flavonoids from Saraca asoca with antioxidant activity
inferredcites →https://doi.org/10.1007/s12272-001-1174-9openalex-snapshot
Anti-oxidative and inhibitory activities on nitric oxide (NO) and prostaglandin E2 (COX-2) production of flavonoids from seeds of Prunus tomentosa Thunberg
inferredcites →https://doi.org/10.1007/s12272-010-1006-7openalex-snapshot
Inflammation and Alzheimer’s disease
inferredcites →https://doi.org/10.1016/0031-9422(90)80144-6openalex-snapshot
Flavanone xyloside and lignans from Prunus jamasakura bark
inferredcites →https://doi.org/10.1016/j.fitote.2011.12.025openalex-snapshot
Antiparasitic antioxidant phenylpropanoids and iridoid glycosides from Tecoma mollis
inferredcites →https://doi.org/10.1016/j.fitote.2013.08.007openalex-snapshot
Five new fawcettimine-related alkaloids from Lycopodium japonicum Thunb
inferredcites →https://doi.org/10.1016/j.fitote.2013.09.011openalex-snapshot
Cytotoxic and antioxidant dihydrobenzofuran neolignans from the seeds of Crataegus pinnatifida
inferredcites →https://doi.org/10.1016/j.fitote.2014.01.012openalex-snapshot
New lignans from the bioactive fraction of Sambucus williamsii Hance and proliferation activities on osteoblastic-like UMR106 cells
inferredcites →https://doi.org/10.1016/j.foodchem.2009.09.092openalex-snapshot
Polymethoxy flavones are responsible for the anti-inflammatory activity of citrus fruit peel
inferredcites →https://doi.org/10.1016/j.foodchem.2011.09.102openalex-snapshot
Compounds in functional food fenugreek spice exhibit anti-inflammatory and antioxidant activities
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Antioxidant properties and phytochemical composition of China-grown pomegranate seeds
inferredcites →https://doi.org/10.1016/j.foodchem.2012.11.010openalex-snapshot
Comparative analyses of seeds of wild fruits of Rubus and Sambucus species from Southern Italy: Fatty acid composition of the oil, total phenolic content, antioxidant and anti-inflammatory properties of the methanolic extracts
inferredcites →https://doi.org/10.1016/j.foodchem.2013.01.101openalex-snapshot
Influence of triterpenoids present in apple peel on inflammatory gene expression associated with inflammatory bowel disease (IBD)
inferredcites →https://doi.org/10.1016/j.foodchem.2013.05.053openalex-snapshot
Total phenolics, antioxidant activity, and functional properties of ‘Tommy Atkins’ mango peel and kernel as affected by drying methods
inferredcites →https://doi.org/10.1016/j.foodchem.2014.03.089openalex-snapshot
Valorization of pomegranate peel from 12 cultivars: Dietary fibre composition, antioxidant capacity and functional properties
inferredcites →https://doi.org/10.1016/j.niox.2006.03.009openalex-snapshot
Estrogen regulation of nitric oxide and inducible nitric oxide synthase (iNOS) in immune cells: Implications for immunity, autoimmune diseases, and apoptosis
inferredcites →https://doi.org/10.1016/j.phytochem.2005.06.019openalex-snapshot
Phenylpropanoid glucosides from leaves of Coussarea hydrangeifolia (Rubiaceae)
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Two new neolignan glycosides from Pittosporum glabratum Lindl.
inferredcites →https://doi.org/10.1016/j.pupt.2007.08.003openalex-snapshot
Inhibition of iNOS expression and NO production by anti-inflammatory steroids
inferredcites →https://doi.org/10.1016/j.scienta.2008.05.022openalex-snapshot
Characterization of Tomentosa cherry (Prunus tomentosa Thunb.) genotypes using SSR markers and morphological traits
inferredcites →https://doi.org/10.1016/s0031-9422(00)80653-6openalex-snapshot
Carbon-13 NMR spectroscopy of steroidal sapogenins and steroidal saponins
inferredcites →https://doi.org/10.1016/s0040-4020(98)00725-xopenalex-snapshot
On the absolute structure of optically active neolignans containing a dihydrobenzo[b]furan skeleton
inferredcites →https://doi.org/10.1016/s0891-5849(00)00252-5openalex-snapshot
Reactive oxygen species, cell signaling, and cell injury
inferredcites →https://doi.org/10.1021/jf1033398openalex-snapshot
Maple Syrup Phytochemicals Include Lignans, Coumarins, a Stilbene, and Other Previously Unreported Antioxidant Phenolic Compounds
inferredcites →https://doi.org/10.1021/jf301888yopenalex-snapshot
Metabolite Profiling of Jaboticaba (Myrciaria cauliflora) and Other Dark-Colored Fruit Juices
inferredcites →https://doi.org/10.1021/jf400487gopenalex-snapshot
Bioactive and Marker Compounds from Two Edible Dark-Colored Myrciaria Fruits and the Synthesis of Jaboticabin
inferredcites →https://doi.org/10.1021/jf801792nopenalex-snapshot
Lignans and Other Constituents of the Fruits of Euterpe oleracea (Açai) with Antioxidant and Cytoprotective Activities
inferredcites →https://doi.org/10.1021/jo010136vopenalex-snapshot
Determination of Absolute Configuration of Acyclic 1,2-Diols with Mo2(OAc)4. 1. Snatzke's Method Revisited
inferredcites →https://doi.org/10.1021/np000145jopenalex-snapshot
Steroidal Saponins from Dracaena surculosa
inferredcites →https://doi.org/10.1021/np200117yopenalex-snapshot
Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations
inferredcites →https://doi.org/10.1021/np9901478openalex-snapshot
Novel Oligorhamnosides from the Stem Bark of Cleistopholis glauca
inferredcites →https://doi.org/10.1038/nature01322openalex-snapshot
Inflammation and cancer
inferredcites →https://doi.org/10.1111/j.1753-4887.2007.tb00354.xopenalex-snapshot
Obesity, Metabolic Syndrome, and Type 2 Diabetes: Inflammatory Basis of Glucose Metabolic Disorders
inferredcites →https://doi.org/10.1146/annurev.nutr.23.011702.073237openalex-snapshot
BIOACTIVE COMPOUNDS IN NUTRITION AND HEALTH-RESEARCH METHODOLOGIES FOR ESTABLISHING BIOLOGICAL FUNCTION: The Antioxidant and Anti-inflammatory Effects of Flavonoids on Atherosclerosis
inferredcites →https://doi.org/10.1248/cpb.48.1084openalex-snapshot
Isolation of Lignan Glucosides and Neolignan Sulfate from the Leaves of Glochidion zeylanicum (Gaertn) A. Juss.
inferredcites →https://doi.org/10.1248/cpb.48.1862openalex-snapshot
Four New Compounds, Ficusal, Ficusesquilignan A, B, and Ficusolide Diacetate from the Heartwood of Ficus microcarpa.
inferredcites →https://doi.org/10.1248/cpb.53.110openalex-snapshot
New Phenolics from the Roots of Symplocos caudata WALL
inferredcites →https://doi.org/10.1248/cpb.c12-00174openalex-snapshot
Antioxidant and Anti-nitric Oxide Components from Quercus glauca
inferredcites →https://doi.org/10.1301/nr.2007.dec.s152-s156openalex-snapshot
Obesity, Metabolic Syndrome, and Type 2 Diabetes: Inflammatory Basis of Glucose Metabolic Disorders
inferredcites →https://doi.org/10.1515/hfsg.1992.46.1.39openalex-snapshot
13C NMR Spectroscopic Studies of Phenylcoumaran and 1,2-Diarylpropane Type Lignin Model Compounds. Part 2. Substituent Effects on13C Chemical Shifts of Aromatic Carbons
inferredcites →https://doi.org/10.2174/1385272803666220131193916openalex-snapshot
Transition Metal Complexes as Auxiliary Chromophores in Chiroptical Studies on Carbohydrates

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Additional file 1 of Investigating the binding affinity, molecular dynamics, and ADMET properties of 2,3-dihydrobenzofuran derivatives as an inhibitor of fungi, bacteria, and virus protein
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