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Pseudoguaianolides and Guaianolides from Inula hupehensis as Potential Anti-inflammatory Agents
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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/anie.198500941openalex-snapshot
Synthesis and Biological Activity of α‐Methylene‐γ‐butyrolactones
inferredcites →https://doi.org/10.1002/anie.200903108openalex-snapshot
The Renaissance of α‐Methylene‐γ‐butyrolactones: New Synthetic Approaches
inferredcites →https://doi.org/10.1002/cbdv.200690041openalex-snapshot
Chemical Constituents of Plants from the Genus Inula
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Intramolecular van der waals interactions and chemical shifts: A model for β‐ and γ‐effects
inferredcites →https://doi.org/10.1007/bf02975329openalex-snapshot
Synthesis of sesquiterpene derivatives as potential antitumor agents; Elemane derivatives
inferredcites →https://doi.org/10.1016/0022-1759(86)90368-6openalex-snapshot
Rapid colorimetric assay for cell growth and survival
inferredcites →https://doi.org/10.1016/0031-9422(79)80042-4openalex-snapshot
Zwei neue pseudoguajanolide aus Telekia speciosa
inferredcites →https://doi.org/10.1016/0031-9422(81)85105-9openalex-snapshot
Seven sesquiterpene lactones from Inula britannica var. chinensis
inferredcites →https://doi.org/10.1016/0031-9422(89)80291-2openalex-snapshot
A seco-guaianolide and other sesquiterpene lactones from Postia bombycina
inferredcites →https://doi.org/10.1016/j.bmcl.2008.12.043openalex-snapshot
Japonicones A–D, bioactive dimeric sesquiterpenes from Inula japonica Thunb.
inferredcites →https://doi.org/10.1016/j.foodchem.2009.10.045openalex-snapshot
Antimicrobial activities of some thymol derivatives from the roots of Inula hupehensis
inferredcites →https://doi.org/10.1016/j.tet.2010.09.091openalex-snapshot
New sesquiterpenes from Inula japonica Thunb. with their inhibitory activities against LPS-induced NO production in RAW264.7 macrophages
inferredcites →https://doi.org/10.1016/s0031-9422(00)82383-3openalex-snapshot
Sesquiterpene lactones from Bedfordia arborescens
inferredcites →https://doi.org/10.1016/s0031-9422(00)83174-xopenalex-snapshot
Pseudoguaianolides carabrone derivatives from Loxothysanus sinuatus
inferredcites →https://doi.org/10.1016/s0031-9422(00)84954-7openalex-snapshot
Pseudoguaianolides and other sesquiterpene lactones from Gaillardia species
inferredcites →https://doi.org/10.1016/s0031-9422(00)88614-8openalex-snapshot
Sesquiterpene lactones. Constituents of diploid and polyploid Ambrosia dumosa Gray
inferredcites →https://doi.org/10.1016/s0031-9422(00)89261-4openalex-snapshot
Carpesiolin from Carpesium abrotanoides
inferredcites →https://doi.org/10.1016/s0040-4020(01)92203-3openalex-snapshot
Optical rotatory dispersion
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/s0040-4020(01)98399-1openalex-snapshot
The constituents of helenium aromaticum (Hook) Bailey
inferredcites →https://doi.org/10.1016/s0968-0896(00)00202-9openalex-snapshot
Structural requirements of sesquiterpene lactones to inhibit LPS-induced nitric oxide synthesis in RAW 264.7 macrophages
inferredcites →https://doi.org/10.1016/s0968-0896(97)00003-5openalex-snapshot
Helenanolide-type sesquiterpene lactones—III. Rates and stereochemistry in the reaction of helenalin and related helenanolides with sulfhydryl containing biomolecules
inferredcites →https://doi.org/10.1021/ja00168a020openalex-snapshot
Ab initio IGLO studies of the conformational dependencies of .alpha.-, .beta.-, and .gamma.-substituent effects in the carbon-13 NMR spectra of aliphatic and alicyclic hydrocarbons
inferredcites →https://doi.org/10.1021/ja00445a001openalex-snapshot
Proximity and conformational effects on carbon-13 chemical shifts at the .gamma. position in hydrocarbons
inferredcites →https://doi.org/10.1021/ja00997a001openalex-snapshot
Carbon-13 magnetic resonance. VII. Steric perturbation of the carbon-13 chemical shift
inferredcites →https://doi.org/10.1021/ja01497a055openalex-snapshot
Syntheses in the Cardiac Aglycone Field. III.1 The Conversion of a 14α- to a 14β-Hydroxy Group in the Androstane Series. The Ultraviolet Spectra of Δ15-Androsten-17-ones
inferredcites →https://doi.org/10.1021/jo01059a002openalex-snapshot
The Sesquiterpenoid Lactones of Helenium Bigelovii Gray
inferredcites →https://doi.org/10.1021/np000211hopenalex-snapshot
Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla
inferredcites →https://doi.org/10.1021/np050437qopenalex-snapshot
Sesquiterpene Lactones from Inula britannica and Their Cytotoxic and Apoptotic Effects on Human Cancer Cell Lines
inferredcites →https://doi.org/10.1021/np100124aopenalex-snapshot
Sesquiterpenoids from Inula lineariifolia Inhibit Nitric Oxide Production
inferredcites →https://doi.org/10.1021/np960506oopenalex-snapshot
Sesquiterpene Lactones and Thymol Esters from Vicoa pentanema
inferredcites →https://doi.org/10.1021/np990271ropenalex-snapshot
Acylated Flavonol Glycosides from the Flower of Inula britannica
inferredcites →https://doi.org/10.1023/a:1010391930508openalex-snapshot
Crystal Structure and Absolute Configuration of 6α-Acetoxy-4-oxo-(1αH, 7αH, 8βH, 10βH)-15(4 → 5β)abeo-guaia-2,11(13)-dien-8,12-olide
inferredcites →https://doi.org/10.1039/c0cc03572fopenalex-snapshot
Neojaponicone A, a bioactive sesquiterpene lactone dimer with an unprecedented carbon skeleton from Inula japonica
inferredcites →https://doi.org/10.1055/s-0029-1186065openalex-snapshot
Japonicones E–L, Dimeric Sesquiterpene Lactones fromInula japonicaThunb.
inferredcites →https://doi.org/10.1055/s-2003-41123openalex-snapshot
Sesquiterpenes and Other Constituents from the Aerial Parts ofInula japonica
inferredcites →https://doi.org/10.1055/s-2003-45141openalex-snapshot
Anti-Inflammatory Compounds of Plant Origin. Part I. Action on Arachidonic Acid Pathway, Nitric Oxide and Nuclear Factor κ B (NF-κB)
inferredcites →https://doi.org/10.1055/s-2005-873189openalex-snapshot
New Sesquiterpene Dimers fromInula britannicaInhibit NF-κB Activation and NO and TNF-α Production in LPS-Stimulated RAW264.7 Cells
inferredcites →https://doi.org/10.1055/s-2006-957843openalex-snapshot
Cytotoxicity and NMR Spectral Assigments of Ergolide and Bigelovin
inferredcites →https://doi.org/10.1074/jbc.273.50.33508openalex-snapshot
The Anti-inflammatory Sesquiterpene Lactone Helenalin Inhibits the Transcription Factor NF-κB by Directly Targeting p65
inferredcites →https://doi.org/10.1139/v68-251openalex-snapshot
Franserin and confertin: new pseudoguaianolides isolated from franseria and ambrosia species
inferredcites →https://doi.org/10.1248/bpb.29.455openalex-snapshot
Anti-diabetic and Hypolipidemic Effects of Aqueous-Extract from the Flower of Inula japonica in Alloxan-Induced Diabetic Mice
inferredcites →https://doi.org/10.4049/jimmunol.163.10.5617openalex-snapshot
The Antiinflammatory Sesquiterpene Lactone Parthenolide Inhibits NF-κB by Targeting the IκB Kinase Complex
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.4674500openalex-extracted
Carpesabrolide a, a Succinic Acid-Guaiane Merosesquiterpenoid with Anti-Inflammatory Activity from Carpesium Abrotanoides
inferred← citeshttps://doi.org/10.1002/cbdv.201400080openalex-snapshot
Metabolomic Profile of the Genus Inula
inferred← citeshttps://doi.org/10.1002/cbdv.201400316openalex-snapshot
Essential Oils and Diethyl Ether Extracts of Serbian Xeranthemum cylindraceum and X. annum: Chemical Composition, Antimicrobial Activity, and Chemotaxonomic Implications
inferred← citeshttps://doi.org/10.1002/cbdv.202400265openalex-snapshot
Sesquiterpene Acids and Lactones from Inula Confertiflora with their Antibacterial Activities
inferred← citeshttps://doi.org/10.1002/cbdv.202402492openalex-snapshot
Sesquiterpene Monomers and Dimers From the Flower of Inula japonica Thunb. With Selective Antiproliferation Against Breast Cancer Cells
inferred← citeshttps://doi.org/10.1002/rcm.6677openalex-snapshot
Identification and structural characterization of dimeric sesquiterpene lactones in Inula japonica Thunb. by high‐performance liquid chromatography/electrospray ionization with multi‐stage mass spectrometry
inferred← citeshttps://doi.org/10.1007/s00764-022-00218-9openalex-snapshot
Simultaneous high-performance thin-layer chromatography analysis of phytoconstituents and antioxidant potential of Inula grandiflora Willd. from India
inferred← citeshttps://doi.org/10.1007/s10600-013-0754-2openalex-snapshot
Chemical Constituents from Inula wissmanniana
inferred← citeshttps://doi.org/10.1007/s10600-016-1719-zopenalex-snapshot
Butyrolactones from the Fermentation Products of the Endophytic Fungus Aspergillus versicolor
inferred← citeshttps://doi.org/10.1007/s12272-013-0135-1openalex-snapshot
Five new sesquiterpene lactones from Inula hupehensis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103973openalex-snapshot
Sesquiterpenoids isolated from the flower of Inula japonica as potential antitumor leads for intervention of paclitaxel-resistant non-small-cell lung cancer
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105066openalex-snapshot
Bioactive sesquiterpenes from Inula helenium
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105817openalex-snapshot
Natural terpenoids with anti-inflammatory activities: Potential leads for anti-inflammatory drug discovery
inferred← citeshttps://doi.org/10.1016/j.bse.2012.02.016openalex-snapshot
Terpenoids from Inula sericophylla Franch. and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.bse.2025.105014openalex-snapshot
Chemical constituents from Dictamnus dasycarpus Turcz. and their chemotaxonomy value
inferred← citeshttps://doi.org/10.1016/j.bse.2025.105018openalex-snapshot
Chemical constituents from the flowers of Inula japonica: Chemotaxonomic significance and antidiabetic activity
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.07.018openalex-snapshot
Selective cytotoxicity, inhibition of cell cycle progression, and induction of apoptosis in human breast cancer cells by sesquiterpenoids from Inula lineariifolia Turcz.
inferred← citeshttps://doi.org/10.1016/j.fct.2018.12.029openalex-snapshot
Bioassay-guided isolation of cytotoxic compounds from Chrysophthalmum montanum (DC.) Boiss
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.03.013openalex-snapshot
New sesquiterpenic acids from Inula wissmanniana
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.2019.104292openalex-snapshot
Bioactive sesquiterpenoids and sesquiterpenoid glucosides from the flowers of Inula japonica
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104408openalex-snapshot
Sesquiterpenes and diterpenes from Euphorbia thymifolia
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104454openalex-snapshot
Lineariifolianoids M-O, three rare sesquiterpene lactone dimers inhibiting NO production from Inula lineariifolia
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105762openalex-snapshot
Six undescribed guaianolide-type sesquiterpenes from the aerial parts of Daphne penicillata
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106987openalex-snapshot
Sesquiterpenoid monomers and dimers from the flower of Inula japonica Thunb. with antihepatoma activity
inferred← citeshttps://doi.org/10.1016/j.indcrop.2015.03.039openalex-snapshot
Confertin and scopoletin from leaf and root extracts of Hypochaeris radicata have anti-inflammatory and antioxidant activities
inferred← citeshttps://doi.org/10.1016/j.jep.2014.04.010openalex-snapshot
The genus Inula and their metabolites: From ethnopharmacological to medicinal uses
inferred← citeshttps://doi.org/10.1016/j.phytochem.2013.10.006openalex-snapshot
Bioactive eudesmane and germacrane derivatives from Inula wissmanniana Hand.-Mazz.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113712openalex-snapshot
Seven undescribed compounds from the flower heads of Helianthus annuus L.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114377openalex-snapshot
Undescribed cytotoxic butenolides; asperterreunolides A-E, isolated from endophytic fungus Aspergillus terreus derived from Artemisia arborescens L. supported with in silico study
inferred← citeshttps://doi.org/10.1016/j.phytol.2016.03.014openalex-snapshot
Antioxidant aromatic butenolides from an insect-associated Aspergillus iizukae
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.09.014openalex-snapshot
Aspidsaponins E-H, Four new steroidal saponins from the rhizomes of Aspidistra elatior Blume and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.prmcm.2023.100263openalex-snapshot
Novel multi-target therapeutic potential of the genus Inula: Advances and opportunities for neuroprotection
inferred← citeshttps://doi.org/10.1016/j.sajb.2017.03.040openalex-snapshot
Antioxidant potential and carbohydrate digestive enzyme inhibitory effects of five Inula species and their major compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.01.116openalex-snapshot
Hookerolides A–D, the first naturally occurring C17-pseudoguaianolides from Inula hookeri
inferred← citeshttps://doi.org/10.1016/s1875-5364(17)30062-6openalex-snapshot
Novel natural product therapeutics targeting both inflammation and cancer
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00947openalex-snapshot
Structures and Biological Activities of Polyacylated ent-Kaurane Diterpenoid Glycosides from the Aerial Parts of Inula hupehensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00208openalex-snapshot
Guaianolides and a seco-Eudesmane from the Resinous Exudates of Cushion Bush ( Leucophyta brownii ) and Evaluation of Their Cytostatic and Anti-inflammatory Activity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01106openalex-snapshot
Sesquiterpenes from Inula japonica with Inhibitory Effects on Nitric Oxide Production in Murine Macrophage RAW 264.7 Cells
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03284openalex-snapshot
Heliaquanoids A–E, Five Sesquiterpenoid Dimers from Inula helianthus-aquatica
inferred← citeshttps://doi.org/10.1039/c3fo60041fopenalex-snapshot
Anti-inflammatory effects of phenolic compounds isolated from the flowers of Nymphaea mexicana Zucc.
inferred← citeshttps://doi.org/10.1039/c6ra23092jopenalex-snapshot
Lineariifolianoids I–L, four rare sesquiterpene lactone dimers inhibiting NO production from Inula lineariifolia
inferred← citeshttps://doi.org/10.1039/c7cc05416eopenalex-snapshot
A one-pot tandem chemoselective allylation/cross-coupling via temperature control of a multi-nucleophile/electrophile system
inferred← citeshttps://doi.org/10.1039/d4ra00292jopenalex-snapshot
Carpesabrolide A, a novel meroterpenoid with anti-inflammatory activity from Carpesium abrotanoides
inferred← citeshttps://doi.org/10.1039/d5np00077gopenalex-snapshot
Non-strigolactone natural products interfering with parasitic weed development
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In silico prediction of natural compounds as potential multi-target inhibitors of structural proteins of SARS-CoV-2
inferred← citeshttps://doi.org/10.1080/10496475.2022.2128137openalex-snapshot
Polyphenols in Different Plant Parts of Inula grandiflora Collected from Two Habitats of Uttarakhand Himalayas
inferred← citeshttps://doi.org/10.1080/14786419.2025.2513587openalex-snapshot
Three new ent -kaurene diterpenoid glucosides from the flowers of Inula japonica Thunb.
inferred← citeshttps://doi.org/10.1080/22311866.2013.782757openalex-snapshot
Chemistry and Biochemistry of Terpenoids fromCurcumaand Related Species
inferred← citeshttps://doi.org/10.1111/tpj.13760openalex-snapshot
Discovery of a non‐stereoselective cytochrome P450 catalyzing either 8α‐ or 8β‐hydroxylation of germacrene A acid from the Chinese medicinal plant, Inula hupehensis
inferred← citeshttps://doi.org/10.1142/s0192415x21500166openalex-snapshot
Medicinal Inula Species: Phytochemistry, Biosynthesis, and Bioactivities
inferred← citeshttps://doi.org/10.1517/13543784.2014.868882openalex-snapshot
Inulasesquiterpenoids: structural diversity, cytotoxicity and anti-tumor activity
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Inhibition of Various Cancer Cells Proliferation of Bornyl Acetate and Essential Oil from Inula graveolens (Linnaeus) Desf.
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Anti-Inflammatory, Antiallergic, and COVID-19 Main Protease (Mpro) Inhibitory Activities of Butenolides from a Marine-Derived Fungus Aspergillus terreus
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Phenyl Derivated Butyrolactones from the Fermentation Products of an Endophytic Fungus Aspergillus terreus
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