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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

https://doi.org/10.1002/ejoc.201200725
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4020-8261-0openalex-snapshot
Smallholder Tree Growing for Rural Development and Environmental Services
inferredcites →https://doi.org/10.1007/s11418-007-0177-0openalex-snapshot
Sedative effects of vapor inhalation of agarwood oil and spikenard extract and identification of their active components
inferredcites →https://doi.org/10.1016/j.cclet.2008.05.034openalex-snapshot
A new cytotoxic 2-(2-phenylethyl)chromone from Chinese eaglewood
inferredcites →https://doi.org/10.1016/j.jep.2008.02.005openalex-snapshot
Antinociceptive and anti-inflammatory activities of Aquilaria sinensis (Lour.) Gilg. Leaves extract
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.tetlet.2005.04.072openalex-snapshot
Three novel diepoxy tetrahydrochromones from agarwood artificially produced by intentional wounding
inferredcites →https://doi.org/10.1016/s0006-2952(03)00422-2openalex-snapshot
Inhibition of lipopolysaccharide-induced nitric oxide production by flavonoids in RAW264.7 macrophages involves heme oxygenase-1
inferredcites →https://doi.org/10.1016/s0040-4039(01)95098-1openalex-snapshot
The structure of agarotetrol, a novel highly oxygenated chromone from agarwood(jinko)
inferredcites →https://doi.org/10.1016/s0378-8741(97)00075-5openalex-snapshot
Effect of the aqueous extract of Aquilaria agallocha stems on the immediate hypersensitivity reactions
inferredcites →https://doi.org/10.1021/ar50056a001openalex-snapshot
Exciton chirality method and its application to configurational and conformational studies of natural products
inferredcites →https://doi.org/10.1021/np0503808openalex-snapshot
Neuroprotective 2-(2-Phenylethyl)chromones of Imperata cylindrica
inferredcites →https://doi.org/10.1097/00000658-199503000-00003openalex-snapshot
The Emerging Multifaceted Roles of Nitric Oxide
inferredcites →https://doi.org/10.1107/s0108767383001762openalex-snapshot
On enantiomorph-polarity estimation
inferredcites →https://doi.org/10.1152/physrev.00029.2006openalex-snapshot
Nitric Oxide and Peroxynitrite in Health and Disease
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.33.5088openalex-snapshot
A new chromone from agarwood and pyrolysis products of chromone derivatives.
inferredcites →https://doi.org/10.1248/cpb.34.2766openalex-snapshot
Studies on the agalwood (jinko). IV Structures of 2-(2-phenylethyl)chromone derivatives, agarotetrol and isoagarotetrol.
inferredcites →https://doi.org/10.1248/cpb.34.3033openalex-snapshot
Studies on the agalwood (Jinko). VI Structures of three 2-(2-phenylethyl)-5,6,7,8-tetrahydrochromone derivatives, AH1A, AH2a and AH2b.
inferredcites →https://doi.org/10.1248/cpb.34.4889openalex-snapshot
The structures of AH10 and AH11, nobel bi-phenylethylchromones from agalwood.
inferredcites →https://doi.org/10.1248/cpb.35.4680openalex-snapshot
The structures of AH15 and AH18, new bi- and tri-phenylethylchromones from agalwood.
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.37.124openalex-snapshot
Studies on the agalwood(Jinko). VIII. Structures of bi-phenylethylchromone derivatives.
inferredcites →https://doi.org/10.1248/cpb.37.1428openalex-snapshot
The structure of AH16, new tetrahydroxy-2-(2-phenylethyl)chromone from agalwood.
inferredcites →https://doi.org/10.1248/cpb.39.1869openalex-snapshot
Studies on the Agalwood (Jinko). XI. Structure of Dioxan-Linked Bi-phenylethylchromone Derivative.
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.40.778openalex-snapshot
Studies on the Agalwood "Jikno". XII. Structures of Pentahydroxy-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/10.1271/bbb.100122openalex-snapshot
Agarwood Induced Laxative EffectsviaAcetylcholine Receptors on Loperamide-Induced Constipation in Mice
inferredcites →https://doi.org/10.1631/jzus.b1000330openalex-snapshot
Antitumor and antimicrobial activities of endophytic fungi from medicinal parts of Aquilaria sinensis
inferredcites →https://doi.org/10.22377/ijgp.v2i1.395openalex-snapshot
Antioxidant activity of ethyl acetate extract of Aquilaria agallocha on nitrite-induced methaemoglobin formation P.
inferredcites →https://doi.org/10.3390/molecules14125165openalex-snapshot
A New 2-(2-Phenylethyl)Chromone from Chinese Eaglewood
inferredcites →https://doi.org/10.4103/0973-8258.41185openalex-snapshot
Antioxidant activity of ethyl acetate extract of Aquilaria agallocha on nitrite-induced methaemoglobin formation
inferredcites →https://doi.org/10.4103/0973-8258.82099openalex-snapshot
Anti-inflammatory effects of the ethyl acetate extract of Aquilaria crassna inhibits LPS-induced tumour necrosis factor-alpha production by attenuating P38 MAPK activation

What points at this work

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

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Chemical and Bioactivity Diversity of 2‐(2‐Phenylethyl)chromones in Agarwood: A Review
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Chromones: A Promising Ring System for New Anti‐inflammatory Drugs
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Dysifragilones A–C, Unusual Sesquiterpene Aminoquinones and Inhibitors of NO Production from the South China Sea Sponge Dysidea fragilis
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Identification and quantification of 5,6,7,8‐tetrahydro‐2‐(2‐phenylethyl)chromones in Chinese eaglewood by HPLC with diode array detection and MS
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Fingerprint combining with quantitative analysis of multi‐components by single marker for quality control of Chenxiang Huaqi tablets
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Agarwood as a neuroprotective agent: a comprehensive review of existing evidence and potential avenues for future research
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Production of 2-(2-phenylethyl)chromones in Aquilaria sinensis calli under different treatments
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Chemical constituents with NO production inhibitory and cytotoxic activities from Litsea cubeba
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Three new 5,6,7,8-tetrahydroxy-5,6,7,8-tetrahydrochromone derivatives enantiomeric to agarotetrol from agarwood
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Five new 2-(2-phenylethyl)chromone derivatives from agarwood
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Identification of a diarylpentanoid-producing polyketide synthase in the biosynthesis of 2-(2-phenylethyl)chromones in agarwood
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Euchrestifolines A–O, fifteen novel carbazole alkaloids with potent anti-ferroptotic activity from Murraya euchrestifolia
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Qualitative and Quantitative Analysis of Flidersiachromones in Three Agarwood Samples by HPLC-MS/MS
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Mass spectrometry imaging guided molecular networking to expedite discovery and structural analysis of agarwood natural products
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Rolling deformation characteristics of Chinese eaglewood leaf during drying and rehydration
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Anti-inflammatory 5,6,7,8-tetrahydro-2-(2-phenylethyl)chromones from agarwood of Aquilaria sinensis
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Gastroprotective 2-(2-phenylethyl)chromone-sesquiterpene hybrids from the resinous wood of Aquilaria sinensis (Lour.) Gilg
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5-Hydroxy-2-(2-phenylethyl)chromone (5-HPEC): A novel non-nitrogenous ligand for 5-HT2B receptor
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Aquilaria sinensis (Lour.) Spreng: Phytochemical review and Chemotaxonomic values
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A full solution for multi-component quantification-oriented quality assessment of herbal medicines, Chinese agarwood as a case
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Chromones as a privileged scaffold in drug discovery: A review
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Occurrence, synthesis and biological activity of 2-(2-phenyethyl)chromones
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2-(2-Phenylethyl)chromone derivatives from Chinese agarwood induced by artificial holing
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Anti-neuroinflammatory sesquiterpenes from Chinese eaglewood
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2-(2-Phenylethyl)chromone derivatives in artificial agarwood from Aquilaria sinensis
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Three new sesquiterpenoids from agarwood of Aquilaria crassna
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.08.011openalex-snapshot
Lignans from the stem bark of Syringa pinnatifolia
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Anti-inflammatory 2-(2-phenylethyl)chromone derivatives from Chinese agarwood
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Four new bi-2-(2-phenylethyl)chromone derivatives of agarwood from Aquilaria crassna
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Four new bi-phenylethylchromones from artificial agarwood
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Aquilariaenes A-H, eight new diterpenoids from Chinese eaglewood
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Seven new 2-(2-phenylethyl) chromone derivatives from agarwood of Aquilaria agallocha with inhibitory effects on nitric oxide production
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Dimeric 2-(2-phenethyl)chromones from agarwood of Aquilaria filaria
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Chemical analysis of different parts from agarwood columns by artificially agarwood-inducing method based on GC–MS and UPLC-TOF-MS
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GYF-17, a chloride substituted 2-(2-phenethyl)-chromone, suppresses LPS-induced inflammatory mediator production in RAW264.7 cells by inhibiting STAT1/3 and ERK1/2 signaling pathways
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Natural chromones as potential anti-inflammatory agents: Pharmacological properties and related mechanisms
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Aquilaria spp. (agarwood) as source of health beneficial compounds: A review of traditional use, phytochemistry and pharmacology
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An integrated strategy of marker ingredients searching and near infrared spectroscopy rapid evaluation for the quality control of Chinese eaglewood
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The protective effects of Aquilariae Lignum Resinatum extract on 5-Fuorouracil-induced intestinal mucositis in mice
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5,6,7,8-Tetrahydro-2-(2-phenylethyl)chromones from artificial agarwood of Aquilaria sinensis and their inhibitory activity against acetylcholinesterase
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LC-MS-guided isolation of anti-inflammatory 2-(2-phenylethyl)chromone dimers from Chinese agarwood (Aquilaria sinensis)
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Bi-2-(2-phenethyl)chromone derivatives from agarwood of Aquilaria filaria in the Philippines
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Three new 2-(2-phenylethyl)chromone derivatives from artificial holing agarwood of Aquilaria sinensis
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H2O2 and NADPH oxidases involve in regulation of 2-(2-phenylethyl)chromones accumulation during salt stress in Aquilaria sinensis calli
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An efficient procedure for the preparation of natural products bearing the 2-(2-phenylethyl)chromone skeleton
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Advance in Studies on Chemical Constituents, Pharmacology and Quality Control of Aquilaria sinensis
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Synthesis and Characterization of 5-Hydroxy-2-(2-phenylethyl)chromone (5-HPEC) and Its Analogues as Non-nitrogenous 5-HT2BLigands
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Anti-inflammatory Dimeric 2-(2-Phenylethyl)chromones from the Resinous Wood of Aquilaria sinensis
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Highly Regio- and Enantioselective Catalytic 1,6-Conjugate Addition of Grignard Reagents to Cyclic Dienones
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Soft-enolization Baker–Venkataraman Rearrangement Enabled Total Synthesis of Dirchromones and Related 2-Substituted Chromones
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Phytochemical Constituents of Aquilaria malaccensis Leaf Extract and Their Anti-Inflammatory Activity against LPS/IFN-γ-Stimulated RAW 264.7 Cell Line
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Chromone: A Valid Scaffold in Medicinal Chemistry
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Identification of a diarylpentanoid-producing polyketide synthase revealing an unusual biosynthetic pathway of 2-(2-phenylethyl)chromones in agarwood
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Overview of sesquiterpenes and chromones of agarwood originating from four main species of the genus Aquilaria
inferred← citeshttps://doi.org/10.1039/c9ra02597aopenalex-snapshot
UPLC-MS-guided isolation of single ether linkage dimeric 2-(2-phenylethyl)chromones from Aquilaria sinensis
inferred← citeshttps://doi.org/10.1039/d0np00042fopenalex-snapshot
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A quarter-century journey into 4-chromone derivatives: synthesis, reactions, and pioneering applications thereof
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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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Phenylethylchromones with In Vitro Antitumor Promoting Activity from Aquilaria filaria
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A new prenylated flavone from Pleione bulbocodioides
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New 2-(2-Phenylethyl)chromone derivatives from agarwood originating from Aquilaria sinensis
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Compounds from Aquilaria sinensis against renal fibrosis in vitro
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The structure characteristics, biosynthesis and health benefits of naturally occurring rare flavonoids
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New 2-(2-phenylethyl)chromone derivatives from agarwood and their inhibitory effects on tumor cells
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Human health-related properties of chromones: an overview
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Metabolites associated with endophytic fungi in agarwood: fungal compounds and host metabolites triggered by fungi
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Insect-Resistance of Aquilaria sinensis (Lour.) Leaves is Associated with Volatile Compounds
inferred← citeshttps://doi.org/10.1155/2020/4575030openalex-snapshot
Chemical Constituents and Anti-Inflammatory Effect of Incense Smoke from Agarwood Determined by GC-MS
inferred← citeshttps://doi.org/10.1177/1934578x1601100624openalex-snapshot
New 2-(2-Phenylethyl)chromone Derivatives and Inhibitors of Phosphodiesterase (PDE) 3A from Agarwood
inferred← citeshttps://doi.org/10.1186/s12870-016-0803-7openalex-snapshot
Salinity stress induces the production of 2-(2-phenylethyl)chromones and regulates novel classes of responsive genes involved in signal transduction in Aquilaria sinensis calli
inferred← citeshttps://doi.org/10.1186/s12870-021-03378-8openalex-snapshot
Effects of various artificial agarwood-induction techniques on the metabolome of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1186/s12870-025-07357-1openalex-snapshot
Integrated proteomic and metabolomic analyses reveal the salt-induced agarwood formation mechanism of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1186/s13020-025-01073-6openalex-snapshot
In-depth characterization of minor 2-(2-phenylethyl)chromone oligomers from Chinese agarwood by integrating offline two-dimensional liquid chromatography and hybrid ion trap time-of-flight mass spectrometry
inferred← citeshttps://doi.org/10.1255/ejms.1289openalex-snapshot
A Rapid and Highly Specific Method to Evaluate the Presence of 2-(2-Phenylethyl) Chromones in Agarwood by Supercritical Fluid Chromatography-Mass Spectrometry
inferred← citeshttps://doi.org/10.1371/journal.pone.0327514openalex-snapshot
Effects of different clones and inducing time on agarwood quality in grafted Qi-Nan Aquilaria sinensis (Lour.) spreng
inferred← citeshttps://doi.org/10.14233/ajchem.2023.23442openalex-snapshot
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inferred← citeshttps://doi.org/10.2171/jao.53.242openalex-snapshot
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inferred← citeshttps://doi.org/10.3126/ijasbt.v9i1.35984openalex-snapshot
Economic Value of Agarwood and Its Prospects of Cultivation
inferred← citeshttps://doi.org/10.3389/fpls.2024.1320226openalex-snapshot
Anatomical, chemical and endophytic fungal diversity of a Qi-Nan clone of Aquilaria sinensis (Lour.) Spreng with different induction times
inferred← citeshttps://doi.org/10.3390/ijms17050771openalex-snapshot
Analysis of 2-(2-Phenylethyl)chromones by UPLC-ESI-QTOF-MS and Multivariate Statistical Methods in Wild and Cultivated Agarwood
inferred← citeshttps://doi.org/10.3390/molecules181012324openalex-snapshot
Characterization and Determination of 2-(2-Phenylethyl)chromones in Agarwood by GC-MS
inferred← citeshttps://doi.org/10.3390/molecules201119736openalex-snapshot
New Flavones, a 2-(2-Phenylethyl)-4H-chromen-4-one Derivative, and Anti-Inflammatory Constituents from the Stem Barks of Aquilaria sinensis
inferred← citeshttps://doi.org/10.3390/molecules21050555openalex-snapshot
Five 2-(2-Phenylethyl)chromones from Sodium Chloride-Elicited Aquilaria sinensis Cell Suspension Cultures
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.3390/molecules22101612openalex-snapshot
Discriminative Analysis of Different Grades of Gaharu (Aquilaria malaccensis Lamk.) via 1H-NMR-Based Metabolomics Using PLS-DA and Random Forests Classification Models
inferred← citeshttps://doi.org/10.3390/molecules23020289openalex-snapshot
2-(2-Phenylethyl)-4H-chromen-4-one Derivatives from the Resinous Wood of Aquilaria sinensis with Anti-Inflammatory Effects in LPS-Induced Macrophages
inferred← citeshttps://doi.org/10.3390/molecules23020342openalex-snapshot
Chemical Constituents and Pharmacological Activity of Agarwood and Aquilaria Plants
inferred← citeshttps://doi.org/10.3390/molecules26164886openalex-snapshot
Overview of the Antioxidant and Anti-Inflammatory Activities of Selected Plant Compounds and Their Metal Ions Complexes
inferred← citeshttps://doi.org/10.3390/molecules27113386openalex-snapshot
Agarwood—The Fragrant Molecules of a Wounded Tree
inferred← citeshttps://doi.org/10.3390/molecules30091984openalex-snapshot
2-(2-Phenylethyl)chromone-Sesquiterpene Hybrids from Agarwood of Aquilaria sinensis: Characterization and Biological Activity Evaluation
inferred← citeshttps://doi.org/10.56042/ijnpr.v11i3.30892openalex-snapshot
Aquilaria species as potential anti-inflammatory agents–A review on in vitro and in vivo studies
inferred← citeshttps://doi.org/10.6084/m9.figshare.17193888openalex-snapshot
Additional file 1 of Effects of various artificial agarwood-induction techniques on the metabolome of Aquilaria sinensis
inferred← citeshttps://doi.org/10.6084/m9.figshare.17193891openalex-snapshot
Additional file 2 of Effects of various artificial agarwood-induction techniques on the metabolome of Aquilaria sinensis
inferred← citeshttps://doi.org/10.6084/m9.figshare.17193894openalex-snapshot
Additional file 3 of Effects of various artificial agarwood-induction techniques on the metabolome of Aquilaria sinensis
inferred← citeshttps://doi.org/10.6084/m9.figshare.17193897openalex-snapshot
Additional file 4 of Effects of various artificial agarwood-induction techniques on the metabolome of Aquilaria sinensis
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