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Eight New 2‐(2‐Phenylethyl)chromone (=2‐(2‐Phenylethyl)‐4 H ‐1‐benzopyran‐4‐one) Derivatives from Aquilaria malaccensis Agarwood

https://doi.org/10.1002/hlca.201200069
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Outgoing claims: the papers this work cites, builds on, or argues with.

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/10.1016/0031-9422(93)85039-topenalex-snapshot
Fragrant sesquiterpenes from agarwood
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/s0040-4020(01)82208-0openalex-snapshot
Terpenoids—LXII
inferredcites →https://doi.org/10.1016/s0040-4039(01)82745-3openalex-snapshot
Structure, stereochemistry and absolute configuration of agarol, a new sesquiterpene alcohol from agarwood oil
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/10.1080/00275514.1996.12026716openalex-snapshot
Phaeoacremonium gen. nov. Associated with Wilt and Decline Diseases of Woody Hosts and Human Infections
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.34.4889openalex-snapshot
The structures of AH10 and AH11, nobel bi-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.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

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4007110openalex-extracted
inferred← citeshttps://doi.org/10.1002/pca.70082openalex-snapshot
Phytochemical Diversity and Evolving Strategies for the Quality Evaluation of Agarwood
inferred← citeshttps://doi.org/10.1007/978-3-030-14116-5_169-1openalex-snapshot
Aquilaria malaccensis Lam. Thymelaeaceae
inferred← citeshttps://doi.org/10.1007/978-3-030-38389-3_169openalex-snapshot
Aquilaria malaccensis Lam. Thymelaeaceae
inferred← citeshttps://doi.org/10.1007/978-3-031-26629-4_1openalex-snapshot
Naturally Occurring Organohalogen Compounds—A Comprehensive Review
inferred← citeshttps://doi.org/10.1007/s10600-018-2252-zopenalex-snapshot
A New 2-(2-Phenylethyl)Chromone From Aquilaria sinensis
inferred← citeshttps://doi.org/10.1007/s11101-017-9518-0openalex-snapshot
A review of chemistry, quality and analysis of infected agarwood tree (Aquilaria sp.)
inferred← citeshttps://doi.org/10.1007/s11676-018-00875-9openalex-snapshot
Identification of chemical compounds in agarwood-producing species Aquilaria malaccensis and Gyrinops versteegii
inferred← citeshttps://doi.org/10.1007/s13659-022-00334-3openalex-snapshot
Bioassay-guided isolation of cytotoxic constituents from the flowers of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1007/s40242-018-7273-4openalex-snapshot
Qualitative and Quantitative Analysis of Flidersiachromones in Three Agarwood Samples by HPLC-MS/MS
inferred← citeshttps://doi.org/10.1016/j.chroma.2018.05.018openalex-snapshot
A full solution for multi-component quantification-oriented quality assessment of herbal medicines, Chinese agarwood as a case
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.2014.07.011openalex-snapshot
2-(2-Phenylethyl)chromone derivatives from Chinese agarwood induced by artificial holing
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.01.011openalex-snapshot
2-(2-Phenylethyl)chromone derivatives in artificial agarwood from Aquilaria sinensis
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.02.009openalex-snapshot
Anti-inflammatory 2-(2-phenylethyl)chromone derivatives from Chinese agarwood
inferred← citeshttps://doi.org/10.1016/j.fitote.2017.03.008openalex-snapshot
Four new bi-2-(2-phenylethyl)chromone derivatives of agarwood from Aquilaria crassna
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.02.031openalex-snapshot
Five new epoxy-5,6,7,8-tetrahydro-2-(2-phenylethyl)chromones from Chinese agarwood by artificial holing
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.2023.105564openalex-snapshot
Eight new 2-(2-phenylethyl)chromone derivatives from agarwood of Aquilaria sinensis with anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106312openalex-snapshot
Anti-inflammatory 5,6,7,8-tetrahydro-2-(2-phenylethyl) chromone derivatives from the stems of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.119841openalex-snapshot
Analysis of the quality and characteristic chemical components of agarwood based on the drilling method for Qi-Nan agarwood
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.122698openalex-snapshot
Bioactivity and in silico insights into 2-(2-phenylethyl)-4H-chromen-4-one and sesquiterpenoid constituents from agarwood (Aquilaria sinensis) as anti-inflammatory agents
inferred← citeshttps://doi.org/10.1016/j.intimp.2016.03.044openalex-snapshot
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
inferred← citeshttps://doi.org/10.1016/j.intimp.2018.12.048openalex-snapshot
GYF-21, an epoxide 2‑(2‑phenethyl)‑chromone derivative, suppresses dysfunction of B cells mainly via inhibiting BAFF activated signaling pathways
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.phytol.2018.05.008openalex-snapshot
Three new 2-(2-phenylethyl)chromone derivatives from artificial holing agarwood of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1016/j.phytol.2022.07.009openalex-snapshot
Three new 2-(2-phenylethyl)chromones from ‘Chong-lou’ agarwood of Aquilaria sinensis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151355openalex-snapshot
Malacinones A and B, two novel sesquiterpenoids with 6/6/5 tricyclic ring system from the agarwood of Aquilaria malaccensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00462openalex-snapshot
Aquilanols A and B, Macrocyclic Humulene-Type Sesquiterpenoids from the Agarwood of Aquilaria malaccensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00635openalex-snapshot
Adiponectin-Secretion-Promoting Phenylethylchromones from the Agarwood of Aquilaria malaccensis
inferred← citeshttps://doi.org/10.1021/cr400265zopenalex-snapshot
Chromone: A Valid Scaffold in Medicinal Chemistry
inferred← citeshttps://doi.org/10.1039/c8ra09409hopenalex-snapshot
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
Natural products in agarwood and Aquilaria plants: chemistry, biological activities and biosynthesis
inferred← citeshttps://doi.org/10.1055/a-0645-1437openalex-snapshot
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
inferred← citeshttps://doi.org/10.1055/s-0042-110858openalex-snapshot
Phenylethylchromones with In Vitro Antitumor Promoting Activity from Aquilaria filaria
inferred← citeshttps://doi.org/10.1080/14786419.2014.991323openalex-snapshot
Natural occurring 2-(2-phenylethyl) chromones, structure elucidation and biological activities
inferred← citeshttps://doi.org/10.1080/14786419.2019.1672066openalex-snapshot
Three new 5,6,7,8-tetrahydro-2-(2-phenylethyl)chromones and one new dimeric 2-(2-phenylethyl)chromone from agarwood of Aquilaria crassna Pierre ex Lecomte in Laos
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/10.22376/ijpbs.2017.8.3.p67-72openalex-snapshot
Screening of anticancer activities from agarwood's Methanol extract (gyrinops verstegii [gilg.] Domke)
inferred← citeshttps://doi.org/10.3126/ijasbt.v9i1.35984openalex-snapshot
Economic Value of Agarwood and Its Prospects of Cultivation
inferred← citeshttps://doi.org/10.33545/26631067.2020.v2.i2a.49openalex-snapshot
Boosting up the economy of Pakistan through agarwood production
inferred← citeshttps://doi.org/10.3389/fpls.2019.00122openalex-snapshot
Agarwood Induction: Current Developments and Future Perspectives
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/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/molecules21111433openalex-snapshot
Four New 2-(2-Phenylethyl)chromone Derivatives from Chinese Agarwood Produced via the Whole-Tree Agarwood-Inducing Technique
inferred← citeshttps://doi.org/10.3390/molecules23020342openalex-snapshot
Chemical Constituents and Pharmacological Activity of Agarwood and Aquilaria Plants
inferred← citeshttps://doi.org/10.3390/molecules23061261openalex-snapshot
Monitoring the Chemical Profile in Agarwood Formation within One Year and Speculating on the Biosynthesis of 2-(2-Phenylethyl)Chromones
inferred← citeshttps://doi.org/10.3390/molecules27113386openalex-snapshot
Agarwood—The Fragrant Molecules of a Wounded Tree
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