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Four New 2-(2-Phenylethyl)-4H-chromen-4-one Derivatives from the Resinous Wood of Aquilaria sinensis and Their Inhibitory Activities on Neutrophil Pro-Inflammatory Responses
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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/ejoc.201200725openalex-snapshot
Nine 2‐(2‐Phenylethyl)chromone Derivatives from the Resinous Wood of Aquilaria sinensis and Their Inhibition of LPS‐Induced NO Production in RAW 264.7 Cells
inferredcites →https://doi.org/10.1002/ffj.2034openalex-snapshot
The volatile and semi‐volatile constituents of agarwood, the infected heartwood of Aquilaria species: a review
inferredcites →https://doi.org/10.1002/hlca.201100409openalex-snapshot
Sesquiterpenoids and 2‐(2‐Phenylethyl)‐4H‐chromen‐4‐one (=2‐(2‐Phenylethyl)‐4H‐1‐benzopyran‐4‐one) Derivatives from Aquilaria malaccensis Agarwood
inferredcites →https://doi.org/10.1002/hlca.201200069openalex-snapshot
Eight New 2‐(2‐Phenylethyl)chromone (=2‐(2‐Phenylethyl)‐4 H ‐1‐benzopyran‐4‐one) Derivatives from Aquilaria malaccensis Agarwood
inferredcites →https://doi.org/10.1007/s11882-003-0029-2openalex-snapshot
Neutrophils in asthma pathophysiology
inferredcites →https://doi.org/10.1016/0022-1759(74)90109-4openalex-snapshot
Single-step separation of red blood cells, granulocytes and mononuclear leukocytes on discontinuous density gradients of Ficoll-Hypaque
inferredcites →https://doi.org/10.1016/0031-9422(73)80509-6openalex-snapshot
Sesquiterpenes from Cacalia hastata
inferredcites →https://doi.org/10.1016/0031-9422(80)83072-xopenalex-snapshot
Neue sesquiterpene und norditerpene aus vertretern der gattung Libanothamnus
inferredcites →https://doi.org/10.1016/0031-9422(93)85039-topenalex-snapshot
Fragrant sesquiterpenes from agarwood
inferredcites →https://doi.org/10.1016/j.fitote.2016.01.011openalex-snapshot
2-(2-Phenylethyl)chromone derivatives in artificial agarwood from Aquilaria sinensis
inferredcites →https://doi.org/10.1016/j.micinf.2003.09.009openalex-snapshot
Oxidative killing of microbes by neutrophils
inferredcites →https://doi.org/10.1016/j.phytochem.2011.11.017openalex-snapshot
2-(2-Phenylethyl)chromones from Chinese eaglewood
inferredcites →https://doi.org/10.1016/j.phytochem.2017.04.011openalex-snapshot
5,6,7,8-Tetrahydro-2-(2-phenylethyl)chromones from artificial agarwood of Aquilaria sinensis and their inhibitory activity against acetylcholinesterase
inferredcites →https://doi.org/10.1016/j.tet.2012.01.041openalex-snapshot
Chlorinated chromone and diphenyl ether derivatives from the mangrove-derived fungus Pestalotiopsis sp. PSU-MA69
inferredcites →https://doi.org/10.1016/j.tetlet.2005.04.072openalex-snapshot
Three novel diepoxy tetrahydrochromones from agarwood artificially produced by intentional wounding
inferredcites →https://doi.org/10.1016/s0957-4166(01)00089-1openalex-snapshot
A practical and efficient preparation of (−)-(4aS,5R)-4,4a,5,6,7,8-hexahydro-4a,5-dimethyl-2(3H)-naphthalenone: a key intermediate in the synthesis of (−)-dehydrofukinone
inferredcites →https://doi.org/10.1021/jm980441hopenalex-snapshot
1-Benzopyran-4-one Antioxidants as Aldose Reductase Inhibitors
inferredcites →https://doi.org/10.1038/labinvest.3780067openalex-snapshot
Neutrophils: Molecules, Functions and Pathophysiological Aspects
inferredcites →https://doi.org/10.1055/s-0033-1350647openalex-snapshot
2-(2-Phenylethyl)chromone Derivatives in Chinese Agarwood “Qi-Nan” from Aquilaria sinensis
inferredcites →https://doi.org/10.1071/ch9742505openalex-snapshot
The occurrence of Ergosta-4,6,8(14),22-tetraen-3-one in several fungi
inferredcites →https://doi.org/10.1111/j.1600-0609.1988.tb00219.xopenalex-snapshot
The human neutrophil. Function and dysfunction
inferredcites →https://doi.org/10.1172/jci107236openalex-snapshot
Biological Defense Mechanisms. THE PRODUCTION BY LEUKOCYTES OF SUPEROXIDE, A POTENTIAL BACTERICIDAL AGENT
inferredcites →https://doi.org/10.1248/cpb.30.3791openalex-snapshot
Studies on the agarwood (Jinko). I. Structures of 2-(2-phenylethyl) chromone derivatives.
inferredcites →https://doi.org/10.1248/cpb.36.2417openalex-snapshot
Studies on the agalwood (jinko). VII. Structures of phenylethylchromone derivatives AH7, AH8 and AH9.
inferredcites →https://doi.org/10.1248/cpb.39.207openalex-snapshot
Studies on agalwood (Jinko). X. Structures of 2-(2-phenylethyl)chromone derivatives.
inferredcites →https://doi.org/10.1248/cpb.50.419openalex-snapshot
Six New 2-(2-Phenylethyl)chromones from Agarwood.
inferredcites →https://doi.org/10.1248/cpb.51.560openalex-snapshot
Four New 2-(2-Phenylethyl)chromone Derivatives from Withered Wood of Aquilaria sinensis
inferredcites →https://doi.org/10.3390/molecules18033086openalex-snapshot
Whole-tree Agarwood-Inducing Technique: An Efficient Novel Technique for Producing High-Quality Agarwood in Cultivated Aquilaria sinensis Trees
inferredcites →https://doi.org/10.3390/molecules21030274openalex-snapshot
Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing
inferredcites →https://doi.org/10.3390/molecules21070911openalex-snapshot
Characterization and Analysis of 2-(2-Phenylethyl)-chromone Derivatives from Agarwood (Aquilaria crassna) by Artificial Holing for Different Times
inferredcites →https://doi.org/10.3390/molecules21111433openalex-snapshot
Four New 2-(2-Phenylethyl)chromone Derivatives from Chinese Agarwood Produced via the Whole-Tree Agarwood-Inducing Technique
inferredcites →https://doi.org/10.4049/jimmunol.150.10.4591openalex-snapshot
Cyclosporin H is a potent and selective formyl peptide receptor antagonist. Comparison with N-t-butoxycarbonyl-L-phenylalanyl-L-leucyl-L-phenylalanyl-L- leucyl-L-phenylalanine and cyclosporins A, B, C, D, and E
inferredcites →https://doi.org/10.5012/bkcs.2005.26.9.1464openalex-snapshot
Cytotoxic Activity of Ergosta-4,6,8(14),22-tetraen-3-one from the Sclerotia of Polyporus umbellatus
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/cbdv.202200490openalex-snapshot
Chemical and Bioactivity Diversity of 2‐(2‐Phenylethyl)chromones in Agarwood: A Review
inferred← citeshttps://doi.org/10.1007/s10600-020-03083-2openalex-snapshot
Flavones and Steroids from Leaves and Barks of Aquilaria subintegra
inferred← citeshttps://doi.org/10.1016/j.bcp.2025.116806openalex-snapshot
Discovery of a novel C2-functionalized chromen-4-one scaffold for the development of p38α MAPK signaling inhibitors to mitigate neutrophilic inflammatory responses
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104413openalex-snapshot
Aquilaria sinensis (Lour.) Spreng: Phytochemical review and Chemotaxonomic values
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114397openalex-snapshot
Occurrence, synthesis and biological activity of 2-(2-phenyethyl)chromones
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.04.007openalex-snapshot
Four new guaiane sesquiterpenoids from agarwood of Aquilaria filaria
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105177openalex-snapshot
Seven new 2-(2-phenylethyl) chromone derivatives from agarwood of Aquilaria agallocha with inhibitory effects on nitric oxide production
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105421openalex-snapshot
Seven new 2-(2-phenethyl)chromone derivatives from agarwood of Aquilaria walla
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106012openalex-snapshot
Chemical composition and bioactivity variability of two-step extracts derived from traditional and “QiNan” agarwood (Aquilaria spp.)
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107170openalex-snapshot
Hybrids of 2-phenylchromone with phenylpropanoid from the agarwood of Aquilaria sinensis against renal fibrosis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.114129openalex-snapshot
The formation and quality evaluation of agarwood induced by the fungi in Aquilaria sinensis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.120147openalex-snapshot
2-(2-Phenylethyl)chromone dimers as melanin production inhibitors from agarwood of Gyrinops walla Gaertn
inferred← citeshttps://doi.org/10.1016/j.nexres.2025.101117openalex-snapshot
A critical review on agarwood: biosynthesis, therapeutic potential, trade, and conservation challenges
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112578openalex-snapshot
2-(2-Phenylethyl)chromone derivatives: Promising α-glucosidase inhibitors in agarwood from Aquilaria filaria
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.09.008openalex-snapshot
Filarones A and B, new anti-inflammatory dimeric 2-(2-phenethyl)chromones from agarwood of Aquilaria filaria
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c02632openalex-snapshot
Biosynthesis and Medicinal Value of Flavonoids and Chromones in Agarwood
inferred← citeshttps://doi.org/10.1039/c9ob02690hopenalex-snapshot
Synthesis of chromone-containing polycyclic compounds via palladium-catalyzed [2 + 2 + 1] annulation
inferred← citeshttps://doi.org/10.1039/d0np00042fopenalex-snapshot
Natural products in agarwood and Aquilaria plants: chemistry, biological activities and biosynthesis
inferred← citeshttps://doi.org/10.1080/10408398.2022.2124396openalex-snapshot
The structure characteristics, biosynthesis and health benefits of naturally occurring rare flavonoids
inferred← citeshttps://doi.org/10.1080/13880209.2023.2287658openalex-snapshot
Network pharmacology integrated with experimental verification reveals the antipyretic characteristics and mechanism of Zi Xue powder
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/antibiotics13111074openalex-snapshot
The Therapeutic Potential of Agarwood as an Antimicrobial and Anti-Inflammatory Agent: A Scoping Review
inferred← citeshttps://doi.org/10.3390/f12111532openalex-snapshot
Comparative Analysis of Biological Activity of Artificial and Wild Agarwood
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