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Sesquiterpenes from Artemisia argyi: Absolute Configurations and Biological Activities

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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/(sici)1520-636x(1997)9:5/6<578::aid-chir27>3.0.co;2-kopenalex-snapshot
Application of [Mo2(OAc)4] for determination of absolute configuration of brassinosteroid vic-diols by circular dichroism
inferredcites →https://doi.org/10.1002/chir.1041openalex-snapshot
Absolute stereochemistry of guaianolides, of matricin and its epimers, of yarrow proazulenes, and of chamazulene carboxylic acid
inferredcites →https://doi.org/10.1002/chir.20473openalex-snapshot
The use of X‐ray crystallography to determine absolute configuration
inferredcites →https://doi.org/10.1002/ejoc.200700880openalex-snapshot
Synthesis of Biologically Active Guaianolides with a trans ‐Annulated Lactone Moiety
inferredcites →https://doi.org/10.1002/hlca.200900017openalex-snapshot
Three New Sesquiterpenoids from Chrysanthemum indicum L.
inferredcites →https://doi.org/10.1002/nt.2620010602openalex-snapshot
Search for chlorinated sesquiterpene lactones in the neurotoxic thistle Centaurea solstitialis by liquid chromatography‐mass spectrometry, and model studies on their possible artifactual formation
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/0031-9422(80)85022-9openalex-snapshot
11,13-Dehydrodesacetylmatricarin and other sesquiterpene lactones from Artemisia ludoviciana var. Ludoviciana and the identity of artecanin and chyrsartemin B
inferredcites →https://doi.org/10.1016/0031-9422(90)85114-uopenalex-snapshot
Sesquiterpene lactones from Artemisia herba-alba
inferredcites →https://doi.org/10.1016/0031-9422(95)00763-6openalex-snapshot
Circular dichroism of C-7, C-6 trans-fused guaianolides of Centaurea scoparia
inferredcites →https://doi.org/10.1016/0031-9422(96)00142-2openalex-snapshot
Sesquiterpene lactones from Artemisia lerchiana
inferredcites →https://doi.org/10.1016/j.bse.2004.07.003openalex-snapshot
Sesquiterpene lactones and flavonoids of Achillea depressa
inferredcites →https://doi.org/10.1016/j.fitote.2012.12.005openalex-snapshot
NO inhibitory guaianolide-derived terpenoids from Artemisia argyi
inferredcites →https://doi.org/10.1016/j.phytochem.2006.02.026openalex-snapshot
Cytotoxic constituents of Achillea clavennae from Montenegro
inferredcites →https://doi.org/10.1016/j.tet.2012.04.046openalex-snapshot
Artanomadimers A–F: six new dimeric guaianolides from Artemisia anomala
inferredcites →https://doi.org/10.1016/j.tetlet.2013.07.023openalex-snapshot
Arvestolides A–C, new rare sesquiterpenes from the aerial parts of Artemisia vestita
inferredcites →https://doi.org/10.1016/s0031-9422(00)81057-2openalex-snapshot
Sesquiterpene lactones of artemisia klotzchiana
inferredcites →https://doi.org/10.1016/s0031-9422(02)00197-8openalex-snapshot
Guaianolides from Viguiera gardneri inhibit the transcription factor NF-κB
inferredcites →https://doi.org/10.1016/s0040-4020(01)92818-2openalex-snapshot
Circular dichroism and optical rotatory dispersion of sesquiterpene lactones
inferredcites →https://doi.org/10.1016/s0040-4039(01)87872-2openalex-snapshot
Circular dichroism of sesquiterpene lactones
inferredcites →https://doi.org/10.1016/s0040-4039(01)97799-8openalex-snapshot
The determination of the stereochemistry of five-membered α,β-unsaturated lactones with an exomethylene double bond based on the allylic long-range couplings of exomethylene protons
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/cr000665jopenalex-snapshot
The Assignment of Absolute Configuration by NMR
inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
inferredcites →https://doi.org/10.1021/ja00864a043openalex-snapshot
Inherently Dissymetric Chromophores. Optical Rotatory Dispersion of α,β-Unsaturated Ketones and Conformational Analysis of Cyclohexenones
inferredcites →https://doi.org/10.1021/jm049937ropenalex-snapshot
Quantitative Structure−Activity Relationship of Sesquiterpene Lactones as Inhibitors of the Transcription Factor NF-κB
inferredcites →https://doi.org/10.1021/jo010136vopenalex-snapshot
Determination of Absolute Configuration of Acyclic 1,2-Diols with Mo2(OAc)4. 1. Snatzke's Method Revisited
inferredcites →https://doi.org/10.1021/np0103113openalex-snapshot
Dimeric Guaianolides and a Fulvenoguaianolide from Artemisia myriantha
inferredcites →https://doi.org/10.1021/np0202475openalex-snapshot
New Chemical Constituents of Euphorbia q uinquecostata and Absolute Configuration Assignment by a Convenient Mosher Ester Procedure Carried Out in NMR Tubes
inferredcites →https://doi.org/10.1021/np049954jopenalex-snapshot
Polyol Monoterpenes and Sesquiterpene Lactones from the Pacific Northwest Plant Artemisia s uksdorfii
inferredcites →https://doi.org/10.1021/np0603065openalex-snapshot
Sesquiterpenes from Thapsia nitida var. meridionalis and Thapsia nitida var. nitida
inferredcites →https://doi.org/10.1021/np900462uopenalex-snapshot
Dimeric Guaianolides and Sesquiterpenoids from Artemisia anomala
inferredcites →https://doi.org/10.1039/b606168kopenalex-snapshot
Eudesmane sesquiterpenoids from the Asteraceae family
inferredcites →https://doi.org/10.1039/c3np70047jopenalex-snapshot
Natural sesquiterpenoids
inferredcites →https://doi.org/10.1039/jr9650007211openalex-snapshot
1328. Optical rotatory dispersion. Part XXIV. Lactones
inferredcites →https://doi.org/10.1055/s-0030-1249957openalex-snapshot
Highly Oxygenated Guaianolides fromArtemisia dubia
inferredcites →https://doi.org/10.1107/s0021889807059870openalex-snapshot
Determination of absolute structure using Bayesian statistics on Bijvoet differences
inferredcites →https://doi.org/10.2174/138527210792927717openalex-snapshot
Determination of Absolute Configuration of Natural Products: Theoretical Calculation of Electronic Circular Dichroism as a Tool
inferredcites →https://doi.org/10.2174/138945011798109437openalex-snapshot
Perspectives on Sesquiterpene Lactones in Inflammation and Cancer
inferredcites →https://doi.org/10.2174/1568011053765976openalex-snapshot
Anti-Cancer Potential of Sesquiterpene Lactones: Bioactivity and Molecular Mechanisms

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.2021.112733zenodo-depositor-declared
Guaianolide sesquiterpene lactones from Achillea millefolium L
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112955zenodo-depositor-declared
Guaianolides from Artemisia codonocephala suppress interleukine-1β secretion in macrophages
inferred← citeshttps://doi.org/10.1002/chin.201443192openalex-snapshot
ChemInform Abstract: Sesquiterpenes from Artemisia argyi: Absolute Configurations and Biological Activities.
inferred← citeshttps://doi.org/10.1002/cjoc.202300166openalex-snapshot
Guaiane‐type Sesquiterpenoid Dimers from Artemisia zhongdianensis and Antihepatoma Carcinoma Activity via the p38MAPK Pathway
inferred← citeshttps://doi.org/10.1002/cjoc.202300631openalex-snapshot
Artemsieverolactones A—H, Eight Guaiane‐Type Sesquiterpenoid Trimers from Artemisia sieversiana
inferred← citeshttps://doi.org/10.1002/ejoc.201403487openalex-snapshot
Dysifragilones A–C, Unusual Sesquiterpene Aminoquinones and Inhibitors of NO Production from the South China Sea Sponge Dysidea fragilis
inferred← citeshttps://doi.org/10.1007/s11101-023-09910-yopenalex-snapshot
Artemisia argyi H. Lév. & Vaniot: a comprehensive review on traditional uses, phytochemistry, and pharmacological activities
inferred← citeshttps://doi.org/10.1007/s12272-016-0838-1openalex-snapshot
A new rearranged eudesmane sesquiterpene and bioactive sesquiterpenes from the twigs of Lindera glauca (Sieb. et Zucc.) Blume
inferred← citeshttps://doi.org/10.1007/s12272-023-01466-xopenalex-snapshot
Artemongolins A–K, undescribed germacrane-guaiane sesquiterpenoid dimers from Artemisia mongolica and their antihepatoma activities
inferred← citeshttps://doi.org/10.1016/j.apsb.2020.12.006openalex-snapshot
New guaiane-type sesquiterpenoid dimers from Artemisia atrovirens and their antihepatoma activity
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103268openalex-snapshot
Bioactivity-based analysis and chemical characterization of hypoglycemic and antioxidant components from Artemisia argyi
inferred← citeshttps://doi.org/10.1016/j.bioorg.2019.103551openalex-snapshot
Polyhydroxyl guaianolide terpenoids as potential NF-кB inhibitors induced cytotoxicity in human gastric adenocarcinoma cell line
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106056openalex-snapshot
Artemzhongdianolides A1-A21, antihepatic fibrosis guaiane-type sesquiterpenoid dimers from Artemisia zhongdianensis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109059openalex-snapshot
Sesquiterpenoids from Eupatorium chinense L. induce G0/G1 cell cycle arrest and apoptosis in AGS cell via DNA-PK/AKT/p53 pathway
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.115180openalex-snapshot
Artemisia: a promising plant for the treatment of cancer
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.10.077openalex-snapshot
New terpenoids and thiophene derivatives from the aerial parts of Artemisia sieversiana
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2026.109250openalex-snapshot
Green synthesis of Artemisia argyi-mediated CuFe2O4 nanoparticles: Experimental and theoretical insights into anticancer activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.12.004openalex-snapshot
Lactone ring-opening seco-guaianolide involved heterodimers linked via an ester bond from Artemisia argyi with NO inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104372openalex-snapshot
Sesquiterpenoids from Artemisia argyi and their COXs inhibitory activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104900openalex-snapshot
Cytotoxic guaianolides and seco-guaianolides from Artemisia atrovirens
inferred← citeshttps://doi.org/10.1016/j.jare.2024.12.047openalex-snapshot
Dimeric guaianolide sesquiterpenoids from the flowers of Chrysanthemum indicum ameliorate hepatic steatosis through mitigating SIRT1-mediated lipid accumulation and ferroptosis
inferred← citeshttps://doi.org/10.1016/j.jare.2026.08.044openalex-snapshot
A dual-target modulator of STK11 and PP2Acα from the flowers of Chrysanthemum indicum mitigates drug-induced liver injury
inferred← citeshttps://doi.org/10.1016/j.jpba.2019.112835openalex-snapshot
Quantitative determination of characteristic components from compound of Lysionotus pauciflorus Maxim. by LC–MS/MS and its application to a pharmacokinetic study
inferred← citeshttps://doi.org/10.1016/j.nxmate.2026.103029openalex-snapshot
Electronic structure, reactivity, topological features, and computational pharmacology of Pallensin: An underexplored eudesmanolide-type sesquiterpene lactone
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113428openalex-snapshot
Sesquiterpenoids and triterpenoids with anti-inflammatory effects from Artemisia vulgaris L
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113912openalex-snapshot
Sesquiterpenoids from aged Artemisia argyi and their 3D-QSAR for anti-HBV activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114019openalex-snapshot
Guaianolide sesquiterpenes and their activity from Artemisia mongolica
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114100openalex-snapshot
Artemyriantholides A–K, guaiane-type sesquiterpenoid dimers from Artemisia myriantha var. pleiocephala and their antihepatoma activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114518openalex-snapshot
Artemsieverlides A–M, diverse sesquiterpenoid dimers with antihepatic fibrosis activity isolated from Artemisia sieversiana based on molecular networking
inferred← citeshttps://doi.org/10.1016/j.phytol.2017.11.009openalex-snapshot
Four new sesquiterpenoids from Dendranthema morifolium (Ramat.) kitam flowers
inferred← citeshttps://doi.org/10.1016/j.phytol.2020.01.009openalex-snapshot
Artemargyinolide E, a new sesquiterpene lactone from Artemisia argyi inhibits inflammatory responses via down-regulating NF-κB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.10.008openalex-snapshot
Structural, spectroscopic, and computational characterization of the cleavage product of dimolybdenum(II) core under aerobic conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.081openalex-snapshot
Artesin A, a new cage-shaped dimeric guaianolide from Artemisia sieversiana
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.10.102openalex-snapshot
Structures and absolute stereochemistry of guaiane sesquiterpenoids from the gorgonian Menella woodin
inferred← citeshttps://doi.org/10.1016/s1875-5364(23)60411-xopenalex-snapshot
2,3-Seco and 3-nor guaianolides fromAchillea alpina with antidiabetic activity
inferred← citeshttps://doi.org/10.1021/acs.biochem.4c00706openalex-snapshot
Discovery of Peptidic Siderophore Degradation by Screening Natural Product Profiles in Marine-Derived Bacterial Mono- and Cocultures
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00803openalex-snapshot
A Survey of Recently Discovered Naturally Occurring Organohalogen Compounds
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00844openalex-snapshot
Chlorinated Guaiane-Type Sesquiterpene Lactones of Natural Origin
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00867openalex-snapshot
Highly Oxidized Guaianolide Sesquiterpenoids with Potential Anti-inflammatory Activity from Chrysanthemum indicum
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02681openalex-snapshot
Artemisians A–D, Diseco-guaianolide Involved Heterodimeric [4 + 2] Adducts from Artemisia argyi
inferred← citeshttps://doi.org/10.1038/s41598-017-18841-6openalex-snapshot
New anti-inflammatory guaianes from the Atlantic hydrotherm-derived fungus Graphostroma sp. MCCC 3A00421
inferred← citeshttps://doi.org/10.1039/c8ra01672kopenalex-snapshot
Heteroatom-doped porous carbons derived from moxa floss of different storage years for supercapacitors
inferred← citeshttps://doi.org/10.1039/d2ob02182jopenalex-snapshot
Artemongolides A–F, undescribed sesquiterpenoid dimers from Artemisia mongolica and their antihepatic fibrosis activities
inferred← citeshttps://doi.org/10.1080/10286020.2018.1543281openalex-snapshot
Triterpenoids with α-glucosidase inhibitory activity from Artemisia argyi
inferred← citeshttps://doi.org/10.1080/14786419.2017.1332603openalex-snapshot
Two new flavonoids from Artemisia argyi with their anticoagulation activities
inferred← citeshttps://doi.org/10.1080/14786419.2019.1610754openalex-snapshot
Three new sesquiterpenoids with cytotoxic activity from Artemisia argyi
inferred← citeshttps://doi.org/10.1080/14786419.2019.1680665openalex-snapshot
Sesquiterpenoids from Artemisia argyi and their NO production inhibitory activity in RAW264.7 cells
inferred← citeshttps://doi.org/10.1177/1934578x1701201004openalex-snapshot
Further Guaianolides from Chrysophthalmum montanum
inferred← citeshttps://doi.org/10.1186/s12906-024-04578-zopenalex-snapshot
Isolation and anti-neuroinflammation activity of sesquiterpenoids from Artemisia argyi: computational simulation and experimental verification
inferred← citeshttps://doi.org/10.1248/bpb.b16-00336openalex-snapshot
DNA Barcode for Identifying Folium Artemisiae Argyi from Counterfeits
inferred← citeshttps://doi.org/10.2174/1389557519666190611124539openalex-snapshot
Natural Terpenoids as Neuroinflammatory Inhibitors in LPS-stimulated BV-2 Microglia
inferred← citeshttps://doi.org/10.3389/fchem.2021.698700openalex-snapshot
Guaianolide Sesquiterpenes With Significant Antiproliferative Activities From the Leaves of Artemisia argyi
inferred← citeshttps://doi.org/10.3390/biom10060867openalex-snapshot
Anti-Apoptotic and Antioxidant Effects of 3-Epi-Iso-Seco-Tanapartholide Isolated from Artemisia argyi against Iodixanol-Induced Kidney Epithelial Cell Death
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