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(±)‐Atrachinenins A—C, Three Pairs of Caged C 27 Meroterpenoids from the Rhizomes of Atractylodes chinensis
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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.197201291openalex-snapshot
Dyotropic Rearrangements, a New Class of Orbital‐Symmetry Controlled Reactions. Type I
inferredcites →https://doi.org/10.1002/jccs.200000075openalex-snapshot
Phytochemical and Pharmacological Studies on Chinese Changzhu
inferredcites →https://doi.org/10.1002/jlac.19284600106openalex-snapshot
Synthesen in der hydroaromatischen Reihe
inferredcites →https://doi.org/10.1016/0031-9422(81)83108-1openalex-snapshot
Isoprenoid dihydroquinones from a brown alga, Cystophora sp.
inferredcites →https://doi.org/10.1016/0031-9422(83)83034-9openalex-snapshot
Types of sesquiterpenes from Artemisia filifolia
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.cclet.2020.10.027openalex-snapshot
Hyperterpenoids A and B: Two pairs of unprecedented 6/6/4/6/6 polycyclic cyclobutane meroterpenoids with potent neuroprotective and anti-inflammatory activities from Hypericum beanii
inferredcites →https://doi.org/10.1016/j.fitote.2019.02.021openalex-snapshot
Australeols A−F, neuroprotective meroterpenoids from Ganoderma australe
inferredcites →https://doi.org/10.1016/j.jep.2020.113415openalex-snapshot
Atractylodis Rhizoma: A review of its traditional uses, phytochemistry, pharmacology, toxicology and quality control
inferredcites →https://doi.org/10.1016/j.phytochem.2020.112524openalex-snapshot
Meroterpenoids with diverse structures and anti-inflammatory activities from Rhododendron anthopogonoides
inferredcites →https://doi.org/10.1021/acs.orglett.9b02166openalex-snapshot
Aggreganoids A–F, Carbon-Bridged Sesquiterpenoid Dimers and Trimers from Lindera aggregata
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/s41598-018-32512-0openalex-snapshot
Microbial communities in different regions of the gastrointestinal tract in East Asian finless porpoises (Neophocaena asiaeorientalis sunameri)
inferredcites →https://doi.org/10.1039/c7np00005gopenalex-snapshot
Dyotropic rearrangements in natural product total synthesis and biosynthesis
inferredcites →https://doi.org/10.1039/c7ra09859fopenalex-snapshot
Antiviral and anti-inflammatory meroterpenoids: stachybonoids A–F from the crinoid-derived fungus Stachybotrys chartarum 952
inferredcites →https://doi.org/10.1039/c9np00037bopenalex-snapshot
Naturally occurring [4 + 2] type terpenoid dimers: sources, bioactivities and total syntheses
inferredcites →https://doi.org/10.1039/d0np00018copenalex-snapshot
Meroterpenoid natural products from Streptomyces bacteria – the evolution of chemoenzymatic syntheses
inferredcites →https://doi.org/10.1055/s-2001-15817openalex-snapshot
Further Phenols and Polyacetylenes from the Rhizomes of Atractylodes lancea and their Anti-Inflammatory Activity1
inferredcites →https://doi.org/10.1080/10286020.2011.557662openalex-snapshot
Two new polyacetylenic compounds from Atractylodes chinensis (DC.) Koidz.
inferredcites →https://doi.org/10.1248/cpb.53.1580openalex-snapshot
A New Acetylenic Compound from the Rhizomes of Atractylodes chinensis and Its Absolute Configuration
inferredcites →https://doi.org/10.3390/biom11070957openalex-snapshot
Meroterpenoids: A Comprehensive Update Insight on Structural Diversity and Biology
inferredcites →https://doi.org/10.3390/foods9030300openalex-snapshot
Anticancer Activities of Meroterpenoids Isolated from the Brown Alga Cystoseira usneoides against the Human Colon Cancer Cells HT-29
inferredcites →https://doi.org/10.3390/molecules24234353openalex-snapshot
Triterpenes and Aromatic Meroterpenoids with Antioxidant Activity and Neuroprotective Effects from Ganoderma lucidum
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
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/cjoc.202200100openalex-snapshot
Construction of the Hexacyclic Core of Dispirocochlearoids A—C via a Diels−Alder Reaction
inferred← citeshttps://doi.org/10.1002/cjoc.202200250openalex-snapshot
2D NMR ‐based MatchNat Dereplication Strategy Enables Explosive Discovery of Novel Diterpenoid Alkaloids†
inferred← citeshttps://doi.org/10.1002/cjoc.202300231openalex-snapshot
Meroterpenoids Possessing Diverse Rearranged Skeletons with Anti‐inflammatory Activity from the Mangrove‐Derived Fungus Penicillium sp. HLLG ‐122
inferred← citeshttps://doi.org/10.1002/cjoc.202300275openalex-snapshot
Natural Sesquiterpenoids, Diterpenoids, Sesterterpenoids, and Triterpenoids with Intriguing Structures from 2017 to 2022
inferred← citeshttps://doi.org/10.1007/978-3-032-09901-3_1openalex-snapshot
The Diels–Alder Reaction as a Key Step in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107111openalex-snapshot
Atrachinenins D–S, Novel Meroterpenoids with Geranyl Hydroquinone Moiety from Atractylodes Chinensis by the LC/MS-Based Molecular Decoy and Targeted Isolation
inferred← citeshttps://doi.org/10.1016/s1875-5364(26)61082-5openalex-snapshot
Atramacronins A−P, eudesmane-type sesquiterpenoid dimers from Atractylodes macrocephala with anti-hepatocellular carcinoma activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00546openalex-snapshot
Spicatulides A–G, Phenolic–Monoterpenoid Hybrids from Chloranthus spicatus
inferred← citeshttps://doi.org/10.1021/acsomega.2c03927openalex-snapshot
Chlorfortunones A and B, Two Sesquiterpenoid Dimers, Possessing Dispiro[4,2,5,2]pentadecane-6,10,14-tren Moiety from Chloranthus fortunei
inferred← citeshttps://doi.org/10.1021/jacs.2c09978openalex-snapshot
Total Synthesis of Atrachinenins A and B
inferred← citeshttps://doi.org/10.1039/d2nj02149hopenalex-snapshot
Atrachinenynes A–D, four diacetylenic derivatives with unprecedented skeletons from the rhizomes of Atractylodes chinensis
inferred← citeshttps://doi.org/10.1039/d5cc04296hopenalex-snapshot
Structure revision of meroterpenoid natural products enabled by biomimetic total synthesis
inferred← citeshttps://doi.org/10.1080/14786419.2025.2450218openalex-snapshot
Two new polyacetylenes from the roots of Atractylodes macrocephala
inferred← citeshttps://doi.org/10.1186/s13020-026-01473-2openalex-snapshot
A systematic review on the application, phytochemistry and pharmacological activities of the genus Atractylodes
inferred← citeshttps://doi.org/10.1360/ssv-2024-0161openalex-snapshot
Mechanism-oriented quality research system for traditional Chinese medicine
inferred← citeshttps://doi.org/10.3390/plants13081074openalex-snapshot
Boswellianols A–I, Structurally Diverse Diterpenoids from the Oleo-Gum Resin of Boswellia carterii and Their TGF-β Inhibition Activity
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