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Overview of sesquiterpenes and chromones of agarwood originating from four main species of the genus Aquilaria

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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/ffj.2730070602openalex-snapshot

New Nor‐sesquiterpenoids with 10‐epi‐eudesmane skeleton from agarwood (Aquilaria agallocha Roxb.)

inferredcites →https://doi.org/10.1002/ffj.2730080604openalex-snapshot

New compounds identified in agarwood (Aquilaria agallocha Roxb.)

inferredcites →https://doi.org/10.1002/ffj.2730100306openalex-snapshot

Agarwood oil (Aquilaria agallocha Roxb.). Its composition and eight new valencane‐, eremophilane‐ and vetispirane‐ derivatives

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.201100442openalex-snapshot

Two New 2‐(2‐Phenylethyl)chromen‐4‐ones from Aquilaria sinensis ( Lour. ) Gilg

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/s00606-005-0312-xopenalex-snapshot

TrnL-trnF sequence data imply paraphyly of Aquilaria and Gyrinops (Thymelaeaceae) and provide new perspectives for agarwood identification

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/10.1007/s11418-018-1201-2openalex-snapshot

Three new 5,6,7,8-tetrahydroxy-5,6,7,8-tetrahydrochromone derivatives enantiomeric to agarotetrol from agarwood

inferredcites →https://doi.org/10.1016/0031-9422(89)80391-7openalex-snapshot

Tri-2-(2-phenylethyl)chromones from agalwood

inferredcites →https://doi.org/10.1016/0031-9422(91)83206-zopenalex-snapshot

Guaiane sesquiterpenes from agarwood

inferredcites →https://doi.org/10.1016/0031-9422(91)83727-3openalex-snapshot

Three sesquiterpenes from agarwood

inferredcites →https://doi.org/10.1016/0031-9422(93)85039-topenalex-snapshot

Fragrant sesquiterpenes from agarwood

inferredcites →https://doi.org/10.1016/j.bmc.2006.01.023openalex-snapshot

New sesquiterpene from Vietnamese agarwood and its induction effect on brain-derived neurotrophic factor mRNA expression in vitro

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.fitote.2014.07.011openalex-snapshot

2-(2-Phenylethyl)chromone derivatives from Chinese agarwood induced by artificial holing

inferredcites →https://doi.org/10.1016/j.fitote.2014.11.010openalex-snapshot

Five new eudesmane-type sesquiterpenoids from Chinese agarwood induced by artificial holing

inferredcites →https://doi.org/10.1016/j.fitote.2015.08.009openalex-snapshot

Anti-neuroinflammatory sesquiterpenes from Chinese eaglewood

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.fitote.2016.05.014openalex-snapshot

Five new 5,11-epoxyguaiane sesquiterpenes in agarwood “Qi-Nan” from Aquilaria sinensis

inferredcites →https://doi.org/10.1016/j.fitote.2016.07.014openalex-snapshot

Three new sesquiterpenoids from agarwood of Aquilaria crassna

inferredcites →https://doi.org/10.1016/j.fitote.2017.02.009openalex-snapshot

Anti-inflammatory 2-(2-phenylethyl)chromone derivatives from Chinese agarwood

inferredcites →https://doi.org/10.1016/j.fitote.2017.03.008openalex-snapshot

Four new bi-2-(2-phenylethyl)chromone derivatives of agarwood from Aquilaria crassna

inferredcites →https://doi.org/10.1016/j.fitote.2017.05.012openalex-snapshot

Four new bi-phenylethylchromones from artificial agarwood

inferredcites →https://doi.org/10.1016/j.jep.2016.06.055openalex-snapshot

Aquilaria spp. (agarwood) as source of health beneficial compounds: A review of traditional use, phytochemistry and pharmacology

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.phytochem.2017.08.007openalex-snapshot

Dimeric sesquiterpenoid-4H-chromone derivatives from agarwood of Aquilaria crassna and their cytotoxicity

inferredcites →https://doi.org/10.1016/j.phytol.2014.03.003openalex-snapshot

Fragrant agarofuran and eremophilane sesquiterpenes in agarwood ‘Qi-Nan’ from Aquilaria sinensis

inferredcites →https://doi.org/10.1016/j.phytol.2016.07.017openalex-snapshot

New guaiane and acorane sesquiterpenes in high quality agarwood Qi-Nan from Aquilaria sinensis

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/s0031-9422(00)83839-xopenalex-snapshot

Agarol, a new sesquiterpene from Aquilaria agallocha

inferredcites →https://doi.org/10.1016/s0031-9422(00)84975-4openalex-snapshot

Three fragrant sesquiterpenes of agarwood

inferredcites →https://doi.org/10.1016/s0031-9422(00)98539-xopenalex-snapshot

Jinkohol, a prezizane sesquiterpene alcohol from agarwood

inferredcites →https://doi.org/10.1016/s0040-4020(01)82208-0openalex-snapshot

Terpenoids—LXII

inferredcites →https://doi.org/10.1016/s0040-4020(01)88332-0openalex-snapshot

Preparation of (−)-guaia-1(10),11-dien-15,2-olide and (−)-2α-hydroxyguaia-1(10),11-dien-15-oic acid, fragrant sesquiterpenes in agarwood (Aquilaria agallocha Roxb.)

inferredcites →https://doi.org/10.1016/s0040-4020(01)99225-7openalex-snapshot

Terpenoids—XLVII

inferredcites →https://doi.org/10.1016/s0040-4020(01)99363-9openalex-snapshot

Terpenoids—xli

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/10.1021/acs.jnatprod.7b00462openalex-snapshot

Aquilanols A and B, Macrocyclic Humulene-Type Sesquiterpenoids from the Agarwood of Aquilaria malaccensis

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00919openalex-snapshot

Anti-inflammatory Dimeric 2-(2-Phenylethyl)chromones from the Resinous Wood of Aquilaria sinensis

inferredcites →https://doi.org/10.1021/np50017a010openalex-snapshot

Plant Anticancer Agents. XIX. Constituents of Aquilaria malaccensis

inferredcites →https://doi.org/10.1021/np50048a024openalex-snapshot

A New and a Known Derivatives of 2-(2-Phenylethyl) Chromone from a Kind of Agarwood ("Kanankoh," in Japanese) Originating from Aquilaria agallocha

inferredcites →https://doi.org/10.1038/aps.2012.163openalex-snapshot

New targets for the antitumor activity of gambogic acid in hematologic malignancies

inferredcites →https://doi.org/10.1039/p19830000601openalex-snapshot

Jinkoh-eremol and jinkohol II, two new sesquiterpene alcohols from agarwood

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/10.1080/10286020.2012.704910openalex-snapshot

Two new sesquiterpene derivatives from Chinese eaglewood

inferredcites →https://doi.org/10.1080/10286020.2016.1187602openalex-snapshot

A new 2-(2-phenylethyl)chromone glycoside in Chinese agarwood “Qi-Nan” from Aquilaria sinensis

inferredcites →https://doi.org/10.1080/10286020.2016.1268602openalex-snapshot

Qinanmer, a new compound from Chinese agarwood ‘Qi-Nan’ originating from Aquilaria sinensis

inferredcites →https://doi.org/10.1080/10286020.2017.1379998openalex-snapshot

Two new 2-(2-Hydroxy-2-phenylethyl)chromens from agarwood originating from Aquilaria crassna

inferredcites →https://doi.org/10.1080/10286020903508424openalex-snapshot

Two new 2-(2-phenylethyl)chromones from Chinese eaglewood

inferredcites →https://doi.org/10.1080/10412905.2011.9700468openalex-snapshot

Identification of Odor-active Components of Agarwood Essential Oils from Thailand by Solid Phase Microextraction-GC/MS and GC-O

inferredcites →https://doi.org/10.1080/14786410412331280122openalex-snapshot

Three 2-(2-phenylethyl) chromones and two terpenes from agarwood

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.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/10.1590/s0101-20612010000500033openalex-snapshot

Segurança alimentar de hortaliças orgânicas: aspectos sanitários e nutricionais

inferredcites →https://doi.org/10.19540/j.cnki.cjcmm.2017.0202openalex-snapshot

[A new sesquiterpene from Chinese agarwood induced by artificial holing].

inferredcites →https://doi.org/10.3329/bjp.v4i1.851openalex-snapshot

Analysis of essential oil of eaglewood tree (Aquilaria agallocha Roxb.) by gas chromatography mass spectrometry

inferredcites →https://doi.org/10.3329/bjp.v4i2.2800openalex-snapshot

Chemical composition of leaf and seed essential oil of Coriandrum sativum L. from Bangladesh

inferredcites →https://doi.org/10.3329/bjp.v6i1.7902openalex-snapshot

Mathematical modeling for extraction of essential oil from Aquilaria crassna by hydrodistillation and quality of agarwood oil

inferredcites →https://doi.org/10.3390/molecules14125165openalex-snapshot

A New 2-(2-Phenylethyl)Chromone from Chinese Eaglewood

inferredcites →https://doi.org/10.3390/molecules16064884openalex-snapshot

Comparison of Compositions and Antimicrobial Activities of Essential Oils from Chemically Stimulated Agarwood, Wild Agarwood and Healthy Aquilaria sinensis (Lour.) Gilg Trees

inferredcites →https://doi.org/10.3390/molecules21030274openalex-snapshot

Sesquiterpenoids from Chinese Agarwood Induced by Artificial Holing

inferredcites →https://doi.org/10.3390/molecules21030281openalex-snapshot

Three New Sesquiterpenoids and One New Sesquiterpenoid Derivative from Chinese Eaglewood

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/10.3390/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

inferredcites →https://doi.org/10.4268/cjcmm20121323openalex-snapshot

Sesquiterpenes and monoterpene from Aquilaria sinensis

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112554zenodo-depositor-declared

Neuroprotective compounds from the resinous heartwood of Aquilaria sinensis

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112630zenodo-depositor-declared

Sesquiterpene derivatives from the agarwood of Aquilaria malaccensis and their anti-inflammatory effects on NO production of macrophage RAW 264.7 cells

inferred← citeshttps://doi.org/10.1002/cbdv.71113openalex-snapshot

Aquisinoids A and B: Two New Sesquiterpenoid‐Benzaldehyde Hybrids From Aquilaria Sinensis

inferred← citeshttps://doi.org/10.1002/ffj.70016openalex-snapshot

Characterisation of the Aroma‐Active Compounds of Essential Oil of Kezixiang by Different Extraction Processes Using GC × GC – TOF – MS and GC –O– MS

inferred← citeshttps://doi.org/10.1002/ffj.70066openalex-snapshot

Comparative Metabolic Study of Agarwood From China and Southeast Asia Based on GC – MS , Chemometrics and Bio‐Activity

inferred← citeshttps://doi.org/10.1002/pca.70082openalex-snapshot

Phytochemical Diversity and Evolving Strategies for the Quality Evaluation of Agarwood

inferred← citeshttps://doi.org/10.1007/978-3-030-92030-2_2openalex-snapshot

The Chemistry of Agarwood Odorants

inferred← citeshttps://doi.org/10.1007/978-981-16-8690-0_52openalex-snapshot

kNN: Classification of Agarwood Types in Oil and Wooden Using E-nose

inferred← citeshttps://doi.org/10.1007/s00284-024-04048-2openalex-snapshot

Endophytic Microbial Community Structure and Dynamics Influence Agarwood Formation in Aquilaria malaccensis Lam.

inferred← citeshttps://doi.org/10.1007/s11101-025-10117-6openalex-snapshot

Agarwood as a neuroprotective agent: a comprehensive review of existing evidence and potential avenues for future research

inferred← citeshttps://doi.org/10.1007/s11418-020-01410-zopenalex-snapshot

Five new 2-(2-phenylethyl)chromone derivatives from agarwood

inferred← citeshttps://doi.org/10.1007/s11418-023-01743-5openalex-snapshot

Identification of a diarylpentanoid-producing polyketide synthase in the biosynthesis of 2-(2-phenylethyl)chromones in agarwood

inferred← citeshttps://doi.org/10.1007/s11676-022-01542-wopenalex-snapshot

Identification of sesquiterpene synthase genes in the genome of Aquilaria sinensis and characterization of an α-humulene synthase

inferred← citeshttps://doi.org/10.1007/s12298-021-01040-zopenalex-snapshot

Genome-wide detection and classification of terpene synthase genes in Aquilaria agallochum

inferred← citeshttps://doi.org/10.1007/s13659-021-00313-0openalex-snapshot

Sesquiterpenoids and 2-(2-Phenylethyl)chromone Derivatives from the Resinous Heartwood of Aquilaria sinensis

inferred← citeshttps://doi.org/10.1007/s44372-025-00188-2openalex-snapshot

Treatment with metal–organic frameworks (MOFs) elicits secondary metabolite accumulation in Aquilaria crassna (agarwood) callus culture

inferred← citeshttps://doi.org/10.1016/b978-0-443-40578-5.00004-0openalex-snapshot

Right time for drug development from volatile oils

inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103789openalex-snapshot

Anti-inflammatory 5,6,7,8-tetrahydro-2-(2-phenylethyl)chromones from agarwood of Aquilaria sinensis

inferred← citeshttps://doi.org/10.1016/j.biteb.2023.101337openalex-snapshot

The induction techniques of resinous agarwood formation: A review

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.2020.104542openalex-snapshot

Six new dimeric 2-(2-phenylethyl)chromones from artificial agarwood of Aquilaria sinensis

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.2024.106012openalex-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.2024.106143openalex-snapshot

Four new guaiane sesquiterpenes from Agarwood of Aquilaria sinensis and their biological activity toward renal fibrosis

inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106156openalex-snapshot

Chemical analysis of different parts from agarwood columns by artificially agarwood-inducing method based on GC–MS and UPLC-TOF-MS

inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106296openalex-snapshot

Synthesis and pharmacological activity evaluation of 2-(2-Phenylethyl)chromone analogues: The principal components in agarwood

inferred← citeshttps://doi.org/10.1016/j.foodchem.2023.136400openalex-snapshot

Rapid screening and characterization of 2-(2-phenylethyl)chromones in agarwood by UHPLC-Q-Exactive Orbitrap-MS

inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e35874openalex-snapshot

Comparative transcriptome analysis reveals the differences in wound-induced agarwood formation between Chi-Nan and ordinary germplasm of Aquilaria sinensis

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.123758openalex-snapshot

Genome-wide investigation of Cytochrome P450 superfamily of Aquilaria agallocha: Association with terpenoids and phenylpropanoids biosynthesis

inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115263openalex-snapshot

Three candidate 2-(2-phenylethyl)chromone-producing type III polyketide synthases from Aquilaria sinensis (Lour.) Gilg have multifunctions synthesizing benzalacetones, quinolones and pyrones

inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115908openalex-snapshot

E3 ubiquitin ligase RING3 mediates AsWRKY44 degradation to promote wound-induced sesquiterpene biosynthesis in Aquilaria sinensis

inferred← citeshttps://doi.org/10.1016/j.indcrop.2024.118835openalex-snapshot

Cloning and functional analysis of novel terpene synthase genes from Aquilaria sinensis and insights into the biosynthesis of sesquiterpene

inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.122628openalex-snapshot

Sesquiterpenoids in Agarwood: Composition, biosynthesis, and metabolic regulation

inferred← citeshttps://doi.org/10.1016/j.jchromb.2021.123056openalex-snapshot

An integrated chemical characterization based on FT-NIR, GC–MS and LC-MS for the comparative metabolite profiling of wild and cultivated agarwood

inferred← citeshttps://doi.org/10.1016/j.jep.2024.119037openalex-snapshot

Sesquiterpene-enriched extract of Chinese agarwood (Aquilaria sinensis) alleviates bile reflux gastritis through suppression of gastric mucosal cell apoptosis via the Wnt/β-catenin signaling pathway

inferred← citeshttps://doi.org/10.1016/j.jfluchem.2020.109717openalex-snapshot

Synthesis, experimental and theoretical study of novel 2-haloalkyl (-CF2H, -CCl2H, -CF2CF3)-, 3-bromo and bromomethyl substituted chromones

inferred← citeshttps://doi.org/10.1016/j.micres.2026.128576openalex-snapshot

Fungal-induced rapid agarwood formation in Aquilaria malaccensis with resin quality equivalent to natural agarwood

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.pmpp.2025.102806openalex-snapshot

Integrative pathophysiology of agarwood formation: from fungal entry to metabolite accumulation

inferred← citeshttps://doi.org/10.1021/acs.jafc.3c06394openalex-snapshot

Characterization of SchTPSs Enables Construction of Yeast for the Bioproduction of α-Cadinol and the Related Sesquiterpenes

inferred← citeshttps://doi.org/10.1021/acs.jafc.4c02440openalex-snapshot

Identification of O-Methyltransferases Potentially Contributing to the Structural Diversity of 2-(2-Phenylethyl)chromones in Agarwood

inferred← citeshttps://doi.org/10.1021/acs.jafc.4c06383openalex-snapshot

Sesquiterpenoids in Agarwood: Biosynthesis, Microbial Induction, and Pharmacological Activities

inferred← citeshttps://doi.org/10.1021/acs.jafc.5c02632openalex-snapshot

Biosynthesis and Medicinal Value of Flavonoids and Chromones in Agarwood

inferred← citeshttps://doi.org/10.1021/acsomega.3c05783openalex-snapshot

Agarperoxinols A and B: Two Unprecedented Tricyclic 6/6/7 Rearranged Humulene-Type Sesquiterpenoids That Attenuated the Neuroinflammation in LPS-Stimulated Microglial Models

inferred← citeshttps://doi.org/10.1038/s41467-022-27971-zopenalex-snapshot

Identification of a diarylpentanoid-producing polyketide synthase revealing an unusual biosynthetic pathway of 2-(2-phenylethyl)chromones in agarwood

inferred← citeshttps://doi.org/10.1038/s41598-025-04230-xopenalex-snapshot

Optimization and induction effect evaluation of complex inducer of Aquilaria sinensis based on factorial design

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/10.1039/d3gc03708hopenalex-snapshot

A synthetic biology and green bioprocess approach to recreate agarwood sesquiterpenoid mixtures

inferred← citeshttps://doi.org/10.1080/00032719.2021.2005081openalex-snapshot

Characterization of Agarwood by Gas Chromatography–Mass Spectrometry and a Random Forest Model

inferred← citeshttps://doi.org/10.1080/10286020.2026.2661019openalex-snapshot

Compounds from Aquilaria sinensis against renal fibrosis in vitro

inferred← citeshttps://doi.org/10.1080/14786419.2022.2162516openalex-snapshot

A high performance thin layer chromatography (HPTLC) method for the quality assessment of agarwood ( Aquilaria malaccensis ) oil from Northeast India

inferred← citeshttps://doi.org/10.1088/1755-1315/1114/1/012042openalex-snapshot

Diversity of agarwood-inducing fungi from Gyrinops versteegii tree

inferred← citeshttps://doi.org/10.1101/2023.05.08.539809openalex-snapshot

Genome-wide analysis of Respiratory burst oxidase homolog ( Rboh ) genes in Aquilaria species and its association with agarwood formation

inferred← citeshttps://doi.org/10.1101/2023.08.04.551930openalex-snapshot

Genome and transcriptome mining revealed evolutionary insights and tissue-specific expression patterns of Cytochrome P450 superfamily in Aquilaria sinensis

inferred← citeshttps://doi.org/10.1101/2024.08.23.609323openalex-snapshot

Treatment with Metal-Organic Frameworks (MOFs) elicits secondary metabolite accumulation in Aquilaria crassna (Agarwood) callus culture

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/10.1155/2021/5593730openalex-snapshot

Remarkable Phytochemical Characteristics of Chi-Nan Agarwood Induced from New-Found Chi-Nan Germplasm of Aquilaria sinensis Compared with Ordinary Agarwood

inferred← citeshttps://doi.org/10.1186/s12864-021-07965-9openalex-snapshot

A tetraploidization event shaped the Aquilaria sinensis genome and contributed to the ability of sesquiterpenes synthesis

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/10.1371/journal.pone.0277136openalex-snapshot

Fusarium oxysporum infection-induced formation of agarwood (FOIFA): A rapid and efficient method for inducing the production of high quality agarwood

inferred← citeshttps://doi.org/10.15451/ec2026-09-15-20-1-23openalex-snapshot

Agarwood in peril: A systematic review of Philippine Aquilaria lam. (Thymelaeaceae) integrating taxonomy, conservation, and pharmacology

inferred← citeshttps://doi.org/10.21203/rs.3.rs-3861587/v1openalex-snapshot

Examining the Trend in Agarwood Oil Studies for the 5 Recent Years (2019-2023): A Bibliometric Analysis

inferred← citeshttps://doi.org/10.2147/dddt.s559380openalex-snapshot

Anti-Inflammatory Properties of Agarwood (Aquilaria Spp.): An Integrated Review of Phytochemistry, Molecular Mechanisms, and Therapeutic Applications

inferred← citeshttps://doi.org/10.2171/jao.53.242openalex-snapshot

Pivotal enzyme that involved in the biosynthesis of agarwood fragrances leading to development of artificial agarwood

inferred← citeshttps://doi.org/10.2174/1871520621666211013115500openalex-snapshot

Computational Exploration of Anti-Cancer Potential of GUAIANE Dimers from Xylopia vielana by Targeting B-Raf Kinase Using Chemo-Informatics, Molecular Docking, and MD Simulation Studies

inferred← citeshttps://doi.org/10.3389/fphar.2024.1357381openalex-snapshot

Utilizing metabolomics and network analysis to explore the effects of artificial production methods on the chemical composition and activity of agarwood

inferred← citeshttps://doi.org/10.3389/fpls.2023.1326080openalex-snapshot

Genome-wide analysis of respiratory burst oxidase homolog (Rboh) genes in Aquilaria species and insight into ROS-mediated metabolites biosynthesis and resin deposition

inferred← citeshttps://doi.org/10.3389/fpls.2024.1437105openalex-snapshot

2-(2-Phenylethyl)chromones increase in Aquilaria sinensis with the formation of agarwood

inferred← citeshttps://doi.org/10.3390/f15010106openalex-snapshot

Physiological and Endophytic Fungi Changes in Grafting Seedlings of Qi-Nan Clones (Aquilaria sinensis)

inferred← citeshttps://doi.org/10.3390/f15101753openalex-snapshot

Screening and Site Adaptability Evaluation of Qi-Nan Clones (Aquilaria sinensis) in Southern China

inferred← citeshttps://doi.org/10.3390/ijms26178468openalex-snapshot

Agarwood in the Modern Era: Integrating Biotechnology and Pharmacology for Sustainable Use

inferred← citeshttps://doi.org/10.3390/molecules27113483openalex-snapshot

Effective Components and Molecular Mechanism of Agarwood Essential Oil Inhalation and the Sedative and Hypnotic Effects Based on GC-MS-Qtof and Molecular Docking

inferred← citeshttps://doi.org/10.3390/molecules27165350openalex-snapshot

Anti-Cancer Effect of Sesquiterpene and Triterpenoids from Agarwood of Aquilaria sinensis

inferred← citeshttps://doi.org/10.3390/molecules28041667openalex-snapshot

Comprehensive Comparisons between Grafted Kynam Agarwood and Normal Agarwood on Traits, Composition, and In Vitro Activation of AMPK

inferred← citeshttps://doi.org/10.3390/molecules28093900openalex-snapshot

An Enantiospecific Synthesis of 5-epi-α-Bulnesene

inferred← citeshttps://doi.org/10.3390/molecules29020468openalex-snapshot

Solid-Phase Microextraction/Gas Chromatography–Time-of-Flight Mass Spectrometry Approach Combined with Network Pharmacology Analysis to Evaluate the Quality of Agarwood from Different Regions against Anxiety Disorder

inferred← citeshttps://doi.org/10.3390/molecules30020352openalex-snapshot

Characterization and Analysis of 2-(2-Phenylethyl)chromone Derivatives and Sesquiterpenoids from Agarwood of Four “Qi-Nan” Clones (Aquilaria sinensis) with Different Induction Times

inferred← citeshttps://doi.org/10.3390/plants15162474openalex-snapshot

Phytochemical Investigation of Gyrinops vidalii Leaves and Evaluation of the α-Glucosidase Inhibitory Activity of the Isolated Metabolites and Molecular Docking of the Active Compounds

inferred← citeshttps://doi.org/10.36808/if/2026/v152i6/171205openalex-snapshot

Agarwood (Aquilaria malaccensis) Cultivation in Tripura: Opportunities for Sustainable Livelihoods, Trade, and Economic Growth

inferred← citeshttps://doi.org/10.3923/ajps.2024.146.167openalex-snapshot

An Updated Review of Aquilaria Species: Distribution, Chemical Constituents and Authentication Methods

inferred← citeshttps://doi.org/10.6084/m9.figshare.16584338openalex-snapshot

Additional file 1 of A tetraploidization event shaped the Aquilaria sinensis genome and contributed to the ability of sesquiterpenes synthesis

inferred← citeshttps://doi.org/10.6084/m9.figshare.16584341openalex-snapshot

Additional file 2 of A tetraploidization event shaped the Aquilaria sinensis genome and contributed to the ability of sesquiterpenes synthesis

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

inferred← citeshttps://doi.org/10.7717/peerj.15818openalex-snapshot

Identification and characterization of novel sesquiterpene synthases TPS9 and TPS12 from Aquilaria sinensis

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