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Structures and Radical-Scavenging Activities of Phenolic Constituents from the Bark of Picea jezoensis var. jezoensis
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0031-9422(92)83753-lopenalex-snapshot
Lignans from leaves of Juniperus chinensis
inferredcites →https://doi.org/10.1016/0031-9422(94)00807-6openalex-snapshot
21α-hydroxy-3β-methoxyserrat-14-en-30-al and other triterpenoids from the cuticle of Picea jezoensis
inferredcites →https://doi.org/10.1016/s0031-9422(00)89347-4openalex-snapshot
13C NMR spectral analysis of lignans from Araucaria angustifolia
inferredcites →https://doi.org/10.1016/s0040-4020(02)00154-0openalex-snapshot
Jezananals A and B: two novel skeletal triterpene aldehydes from the stem bark of Picea jezoensis var. jezoensis
inferredcites →https://doi.org/10.1016/s0140-6736(82)90293-8openalex-snapshot
FIRST PROOF THAT VITAMIN E IS MAJOR LIPID-SOLUBLE, CHAIN-BREAKING ANTIOXIDANT IN HUMAN BLOOD PLASMA
inferredcites →https://doi.org/10.1016/s0304-3835(01)00650-4openalex-snapshot
Cancer chemopreventive agents, serratane-type triterpenoids from Picea jezoensis
inferredcites →https://doi.org/10.1021/ed060p465openalex-snapshot
The intriguing biological role of vitamin E
inferredcites →https://doi.org/10.1021/ja00783a034openalex-snapshot
Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters
inferredcites →https://doi.org/10.1021/jf980431popenalex-snapshot
19F Nuclear Magnetic Resonance Spectroscopy for the Quantitative Detection and Classification of Carbonyl Groups in Lignins
inferredcites →https://doi.org/10.1021/jf9804591openalex-snapshot
Methodology for Identification of Phenolic Acids in Complex Phenolic Mixtures by High-Resolution Two-Dimensional Nuclear Magnetic Resonance. Application to Methanolic Extracts of Two Oregano Species
inferredcites →https://doi.org/10.1021/np020282bopenalex-snapshot
Triterpenoid Constituents Isolated from the Bark of Abies sachalinensis
inferredcites →https://doi.org/10.1021/np049686popenalex-snapshot
Resveratrol Derivatives from the Roots of Vitis thunbergii
inferredcites →https://doi.org/10.1055/s-2001-17360openalex-snapshot
Triterpene Constituents from the Stem Bark of Pinus luchuensis and their DNA Topoisomerase II Inhibitory Effect
inferredcites →https://doi.org/10.1055/s-2003-45153openalex-snapshot
Two New Anti-Tumor Promoting Serratane-Type Triterpenoids from the Stem Bark ofPicea jezoensisvar.jezoensis
inferredcites →https://doi.org/10.1248/cpb.37.2016openalex-snapshot
Effects of the interaction of tannins with Co-existing substances. VI. Effects of tannins and related polyphenols on superoxide anion radical, and on 1,1-diphenyl-2-picrylhydrazyl radical.
inferredcites →https://doi.org/10.3987/com-02-9596openalex-snapshot
Structures and Radical Scavenging Activities of Novel Norstilbene Dimer, Longusone A, and New Stilbene Dimers, Longusols A, B, and C, from Egyptian Herbal Medicine Cyperus longus
inferredcites →https://doi.org/10.3987/com-02-9632openalex-snapshot
Six Flavonostilbenes from Gnetum afircanum and Gnetum gnemon
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.2022.113128zenodo-depositor-declared
Stilbenes: Source plants, chemistry, biosynthesis, pharmacology, application and problems related to their clinical Application-A comprehensive review
inferred← citeshttps://doi.org/10.1002/cbdv.201000147openalex-snapshot
Anti‐Tumor‐Initiating Effects of Spiro‐biflavonoids from Abies sachalinensis
inferred← citeshttps://doi.org/10.1002/hlca.200900032openalex-snapshot
Phenolic Compounds Isolated from the Bark of Abies sachalinensis
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.07.016openalex-snapshot
Anti-tumor-initiating effects of phenolic compounds isolated from the bark of Picea jezoensis var. jezoensis
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.109880openalex-snapshot
Three-step synthesis of flavanostilbenes with a 2-cyclohepten-1-one core by Cu-mediated [5 + 2] cycloaddition/decarboxylation cascade
inferred← citeshttps://doi.org/10.1016/j.foodchem.2012.05.050openalex-snapshot
Picea mariana bark: A new source of trans-resveratrol and other bioactive polyphenols
inferred← citeshttps://doi.org/10.1016/j.phytochem.2015.02.022openalex-snapshot
Interconverting flavonostilbenes with antibacterial activity from Sophora alopecuroides
inferred← citeshttps://doi.org/10.1016/j.phytol.2012.08.007openalex-snapshot
Polygonflavanol A, a novel flavonostilbene glycoside from the roots of Polygonum multiflorum
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70011-xopenalex-snapshot
Chapter 5.3: Five-membered ring systems: furans and benzofurans
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b04871openalex-snapshot
Preparative Isolation of Piceatannol Derivatives from Passion Fruit ( Passiflora edulis ) Seeds by High-Speed Countercurrent Chromatography Combined with High-Performance Liquid Chromatography and Screening for α-Glucosidase Inhibitory Activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00689openalex-snapshot
Flavonostilbenes Isolated from the Stems of Rhamnoneuron balansae as Potential SIRT1 Activators
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00445openalex-snapshot
Synthesis of cis-Oriented Vicinal Diphenylethylenes through a Lewis Acid-Promoted Annulation of Oxotriphenylhexanoates
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00010openalex-snapshot
Cajanusflavanols A–C, Three Pairs of Flavonostilbene Enantiomers from Cajanus cajan
inferred← citeshttps://doi.org/10.1021/np100181copenalex-snapshot
Antioxidant and Anti-inflammatory Phenylpropanoid Derivatives from Calamus quiquesetinervius
inferred← citeshttps://doi.org/10.1021/ol1018147openalex-snapshot
Stereocontrolled Synthesis of Contiguous C(sp3)−C(aryl) Bonds by Lanthanide(III)-Catalyzed Domino Aryl-Claisen [3,3]-Sigmatropic Rearrangements
inferred← citeshttps://doi.org/10.1039/c2np20049jopenalex-snapshot
Natural stilbenoids: distribution in the plant kingdom and chemotaxonomic interest in Vitaceae
inferred← citeshttps://doi.org/10.3390/molecules16032191openalex-snapshot
Tannins of Constant Structure in Medicinal and Food Plants—Hydrolyzable Tannins and Polyphenols Related to Tannins
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