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Anti-Inflammatory Compounds from Atractylodes macrocephala

https://doi.org/10.3390/molecules24101859
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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/ptr.2040openalex-snapshot
Atractylenolide I and atractylenolide III inhibit Lipopolysaccharide‐induced TNF‐ α and NO production in macrophages
inferredcites →https://doi.org/10.1006/abio.2001.5059openalex-snapshot
A Cell-Based Assay System for Monitoring NF-κB Activity in Human HaCaT Transfectant Cells
inferredcites →https://doi.org/10.1007/s10156-008-0619-yopenalex-snapshot
Role of nuclear IκB proteins in the regulation of host immune responses
inferredcites →https://doi.org/10.1016/j.autrev.2016.07.022openalex-snapshot
Parkinson's disease: Autoimmunity and neuroinflammation
inferredcites →https://doi.org/10.1016/j.bbalip.2014.07.008openalex-snapshot
Prostaglandin E2-induced inflammation: Relevance of prostaglandin E receptors
inferredcites →https://doi.org/10.1016/j.biopha.2017.06.036openalex-snapshot
Inducible nitric oxide synthase: Good or bad?
inferredcites →https://doi.org/10.1016/j.bse.2010.12.023openalex-snapshot
Chemical constituents of Atractylodes chinensis (DC.) Koidz.
inferredcites →https://doi.org/10.1016/j.cellimm.2011.06.019openalex-snapshot
Stimulation of Fas (CD95) induces production of pro-inflammatory mediators through ERK/JNK-dependent activation of NF-κB in THP-1 cells
inferredcites →https://doi.org/10.1016/j.ejphar.2009.04.001openalex-snapshot
Inhibitory effect of atractylenolide I on angiogenesis in chronic inflammation in vivo and in vitro
inferredcites →https://doi.org/10.1016/j.ijbiomac.2014.02.019openalex-snapshot
Atractylodes macrocephala polysaccharides induces mitochondrial-mediated apoptosis in glioma C6 cells
inferredcites →https://doi.org/10.1016/j.jep.2007.08.002openalex-snapshot
Screening for the anti-inflammatory activity of fractions and compounds from Atractylodes macrocephala koidz
inferredcites →https://doi.org/10.1016/j.jep.2013.10.005openalex-snapshot
Bioactivity-guided isolation of polyacetylenes with inhibitory activity against NO production in LPS-activated RAW264.7 macrophages from the rhizomes of Atractylodes macrocephala
inferredcites →https://doi.org/10.1016/j.jep.2018.08.023openalex-snapshot
The traditional uses, phytochemistry, and pharmacology of Atractylodes macrocephala Koidz.: A review
inferredcites →https://doi.org/10.1016/j.lfs.2004.10.042openalex-snapshot
Inhibition of inducible nitric oxide synthase and cyclooxygenase II by Platycodon grandiflorum saponins via suppression of nuclear factor-κB activation in RAW 264.7 cells
inferredcites →https://doi.org/10.1016/j.msec.2017.03.291openalex-snapshot
In vitro antibacterial and cytotoxic activities of plasma-modified polyethylene terephthalate nonwoven dressing with aqueous extract of Rhizome Atractylodes macrocephala
inferredcites →https://doi.org/10.1021/np970430bopenalex-snapshot
5-Lipoxygenase and Cyclooxygenase-1 Inhibitory Active Compounds from Atractylodes lancea
inferredcites →https://doi.org/10.1038/cr.2009.137openalex-snapshot
The nuclear signaling of NF-κB: current knowledge, new insights, and future perspectives
inferredcites →https://doi.org/10.1055/s-2006-961013openalex-snapshot
Acetylene ausAtractylis koreana
inferredcites →https://doi.org/10.1080/10286020.2016.1247351openalex-snapshot
Two new compounds from Atractylodes macrocephala with neuroprotective activity
inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06112.xopenalex-snapshot
Activation of p38 MAPK in the substantia nigra leads to nuclear translocation of NF‐κB in MPTP‐treated mice: implication in Parkinson’s disease
inferredcites →https://doi.org/10.1128/mcb.21.9.6461-6469.2001openalex-snapshot
Mitogen-Activated Protein Kinase p38 Controls the Expression and Posttranslational Modification of Tristetraprolin, a Regulator of Tumor Necrosis Factor Alpha mRNA Stability
inferredcites →https://doi.org/10.1146/annurev-physiol-022516-034348openalex-snapshot
Macrophages and the Recovery from Acute and Chronic Inflammation
inferredcites →https://doi.org/10.1152/ajpcell.2001.280.3.c441openalex-snapshot
IFN-γ + LPS induction of iNOS is modulated by ERK, JNK/SAPK, and p38mapkin a mouse macrophage cell line
inferredcites →https://doi.org/10.1155/2014/926381openalex-snapshot
The Metabolism of Polysaccharide from Atractylodes macrocephala Koidz and Its Effect on Intestinal Microflora
inferredcites →https://doi.org/10.1155/2016/2926819openalex-snapshot
Evaluation of Medicinal Categorization of Atractylodes japonica Koidz. by Using Internal Transcribed Spacer Sequencing Analysis and HPLC Fingerprinting Combined with Statistical Tools
inferredcites →https://doi.org/10.1155/2019/8245071openalex-snapshot
Key CMM Combinations in Prescriptions for Treating Mastitis and Working Mechanism Analysis Based on Network Pharmacology
inferredcites →https://doi.org/10.1186/s12199-018-0740-1openalex-snapshot
Inflammation and cancer
inferredcites →https://doi.org/10.1196/annals.1352.026openalex-snapshot
Transcription Factor NF‐κB: A Sensor for Smoke and Stress Signals
inferredcites →https://doi.org/10.1248/cpb.c15-00805openalex-snapshot
Inflammatory Inhibitory Activity of Sesquiterpenoids from Atractylodes macrocephala Rhizomes
inferredcites →https://doi.org/10.3389/fphar.2018.00976openalex-snapshot
Raging the War Against Inflammation With Natural Products
inferredcites →https://doi.org/10.3390/molecules171113457openalex-snapshot
Antioxidant Ability and Mechanism of Rhizoma Atractylodes macrocephala
inferredcites →https://doi.org/10.3748/wjg.v9.i3.553openalex-snapshot
Significance of changes of gastrointestinal peptides in blood and ileum of experimental spleen deficiency rats
inferredcites →https://doi.org/10.3892/mmr.2017.7385openalex-snapshot
Antitumor activity of 2-[(2E)-3,7-dimethyl-2,6-octadienyl]-6-methyl-2,5-cyclohexadiene-1,4-dione isolated from the aerial part of Atractylodes macrocephala in hepatocellular carcinoma
inferredcites →https://doi.org/10.4049/jimmunol.162.1.415openalex-snapshot
Evaluation of the Role of Mitogen-Activated Protein Kinases in the Expression of Inducible Nitric Oxide Synthase by IFN-γ and TNF-α in Mouse Macrophages

What points at this work

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

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Polyacetylenes from the roots of Cirsium japonicum var. ussuriense
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The Rhizome of Atractylodes macrocephala Koidz.: A Comprehensive Review on the Traditional Uses, Phytochemistry and Pharmacology
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Atractylenolide I Alleviates Lipotoxicity in Hepatocytes and Protects NAFLD in Mice Through SIRT1 ‐Dependent IRE1α ‐ XBP1 Pathway
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Effects of PAMK on lncRNA, miRNA, and mRNA expression profiles of thymic epithelial cells
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The regulation effect of Atractylodis macrocephalae polysaccharides on the growth performance, antioxidant capacity and immune function in Litopenaeus vannamei
inferred← citeshttps://doi.org/10.1016/j.arabjc.2023.105137openalex-snapshot
Plant polyacetylenoids: Phytochemical, analytical and pharmacological updates
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Structural characterization of Atractylodes macrocephala polysaccharide 1 and its gut microbiota-mediated alleviation of ulcerative colitis
inferred← citeshttps://doi.org/10.1016/j.ejphar.2020.173735openalex-snapshot
Atractylenolides, essential components of Atractylodes-based traditional herbal medicines: Antioxidant, anti-inflammatory and anticancer properties
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105490openalex-snapshot
Six polyacetylenes from Atractylodes macrocephala Koidz and their anti-colon cancer activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2026.107468openalex-snapshot
Chemical constituents of Roscoea humeana: their anti-inflammatory and GLP-1 secretagogic activity
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115251openalex-snapshot
Inhibition of the Akt/NF-κB pathway is involved in the anti-gastritis effects of an ethanolic extract of the rhizome of Atractylodes macrocephala
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115506openalex-snapshot
Isolation, structure and bioactivity of polysaccharides from Atractylodes macrocephala: A review
inferred← citeshttps://doi.org/10.1016/j.microc.2021.106884openalex-snapshot
Excitation-emission matrix fluorescence spectroscopy combined with chemometrics methods for rapid identification and quantification of adulteration in Atractylodes macrocephala Koidz
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113288openalex-snapshot
Polyacetylenes in herbal medicine: A comprehensive review of its occurrence, pharmacology, toxicology, and pharmacokinetics (2014–2021)
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114761openalex-snapshot
Atractymacronoids A-L, sesquiterpenoids from the rhizomes of Atractylodes macrocephala and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.prmcm.2024.100394openalex-snapshot
A comprehensive pharmacological review of Atractylodes Macrocephala: Traditional uses, phytochemistry, pharmacokinetics, and therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.saa.2021.120737openalex-snapshot
Geographical origin traceability of traditional Chinese medicine Atractylodes macrocephala Koidz. by using multi-way fluorescence fingerprint and chemometric methods
inferred← citeshttps://doi.org/10.1021/acsami.5c08068openalex-snapshot
Medicinal Plant-Derived Carbon Dots Nanozymes Ameliorate Ulcerative Colitis via Anti-inflammatory, Antioxidant, and Gut Barrier-Protective Effects
inferred← citeshttps://doi.org/10.1021/jacs.2c09978openalex-snapshot
Total Synthesis of Atrachinenins A and B
inferred← citeshttps://doi.org/10.1080/14786419.2026.2643920openalex-snapshot
Chemical constituents from Atractylodes japonica and their inhibitory effect on NO production
inferred← citeshttps://doi.org/10.1155/2020/7531967openalex-snapshot
Chinese Herbal Medicines for Rheumatoid Arthritis: Text‐Mining the Classical Literature for Potentially Effective Natural Products
inferred← citeshttps://doi.org/10.1155/2022/2338533openalex-snapshot
Polysaccharides from Rhizoma Atractylodis Macrocephalae: A Review on Their Extraction, Purification, Structure, and Bioactivities
inferred← citeshttps://doi.org/10.1177/0300060521993315openalex-snapshot
Atractylenolide I alleviates ischemia/reperfusion injury by preserving mitochondrial function and inhibiting caspase-3 activity
inferred← citeshttps://doi.org/10.2147/dddt.s582323openalex-snapshot
Medicinal Plants That Modulate Nitric Oxide Synthase Activity: Implications in Inflammation and Oxidative Stress
inferred← citeshttps://doi.org/10.2174/0115734110283469231204061131openalex-snapshot
Quantitative HPLC-based Metabolomics Approach for the Discrimination of Processed Rhizomes of Atractylodes Macrocephala
inferred← citeshttps://doi.org/10.3233/thc-220601openalex-snapshot
Atractylenolide II ameliorates myocardial fibrosis and oxidative stress in spontaneous hypertension rats
inferred← citeshttps://doi.org/10.3389/fgene.2025.1584986openalex-snapshot
Prediction of NR3C1 as a methylation marker for the prevention and treatment of gastric cancer in Rhizoma Atractylodis Macrocephalae based on machine learning algorithm and bioinformatics analysis
inferred← citeshttps://doi.org/10.3389/fmed.2023.1325491openalex-snapshot
Potential therapeutic target for polysaccharide inhibition of colon cancer progression
inferred← citeshttps://doi.org/10.3389/fphar.2021.642685openalex-snapshot
Shenling Baizhu Powder Inhibits RV-SA11-Induced Inflammation and Rotavirus Enteritis via TLR4/MyD88/NF-κB Signaling Pathway
inferred← citeshttps://doi.org/10.3389/fvets.2024.1518433openalex-snapshot
The biological function of Atractylodes lancea and its application in animal husbandry: a review
inferred← citeshttps://doi.org/10.3390/agronomy12071485openalex-snapshot
Effect of Artificial Light Treatment on the Physiological Property and Biological Activity of the Aerial and Underground Parts of Atractylodes macrocephala
inferred← citeshttps://doi.org/10.3390/antiox11040611openalex-snapshot
Anti-Inflammatory and Antioxidant Chinese Herbal Medicines: Links between Traditional Characters and the Skin Lipoperoxidation “Western” Model
inferred← citeshttps://doi.org/10.3390/antiox13070868openalex-snapshot
Traditional Chinese Medicine for Hashimoto’s Thyroiditis: Focus on Selenium and Antioxidant Phytochemicals
inferred← citeshttps://doi.org/10.3390/ijms25010156openalex-snapshot
Unlocking Prognostic Genes and Multi-Targeted Therapeutic Bioactives from Herbal Medicines to Combat Cancer-Associated Cachexia: A Transcriptomics and Network Pharmacology Approach
inferred← citeshttps://doi.org/10.3390/life16091476openalex-snapshot
Pharmacological Effects and Proposed Mechanisms of Atractylodes Medicinal Plants in Liver Diseases: A Narrative Review
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Bioadhesive Polymeric Films Based on Red Onion Skins Extract for Wound Treatment: An Innovative and Eco-Friendly Formulation
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Chrysoeriol ameliorates COX-2 expression through NF-κB, AP-1 and MAPK regulation via the TLR4/MyD88 signaling pathway in LPS-stimulated murine macrophages
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