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Sesquiterpenoid and C 14 -polyacetylene glycosides from the rhizomes of Atractylodes lancea
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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/mrc.2730openalex-snapshot
Guaiane‐type sesquiterpenoid glucosides from Gardenia jasminoides Ellis
inferredcites →https://doi.org/10.1002/pca.2494openalex-snapshot
HPLC/UV Analysis of Polyacetylenes, Phenylpropanoid and Pyrrolidine Alkaloids in Medicinally Used Codonopsis Species
inferredcites →https://doi.org/10.1016/0040-4020(82)85040-0openalex-snapshot
Circular dichroism and stereochemistry of chiral conjugated cyclohexenones
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.carres.2011.06.015openalex-snapshot
New polyacetylene glucosides from the florets of Carthamus tinctorius and their weak anti-inflammatory activities
inferredcites →https://doi.org/10.1016/j.carres.2013.07.011openalex-snapshot
Acyl glycosides with rare β-d-apiofuranosyl-β-d-glucopyranosyl-β-d-apiofuranosyl from Erycibe hainanesis
inferredcites →https://doi.org/10.1016/j.phytochem.2008.04.008openalex-snapshot
Three types of sesquiterpenes from rhizomes of Atractylodes lancea
inferredcites →https://doi.org/10.1016/j.tet.2015.02.041openalex-snapshot
New sesquiterpenoids isolated from Atractylodes lancea fermented by marine fungus
inferredcites →https://doi.org/10.1016/s0031-9422(97)00342-7openalex-snapshot
Diacetoxy-substituted polyacetylenes from Atractylodes lancea
inferredcites →https://doi.org/10.1016/s1995-7645(14)60069-9openalex-snapshot
Therapeutic potential and pharmacological activities of Atractylodes lancea (Thunb.) DC.
inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00066openalex-snapshot
Bioactive Sesquiterpenoid and Polyacetylene Glycosides from Atractylodes lancea
inferredcites →https://doi.org/10.1021/np300310aopenalex-snapshot
Dammarane Glycosides from the Root of Machilus yaoshansis
inferredcites →https://doi.org/10.1021/np400784vopenalex-snapshot
Dibenzoyl and Isoflavonoid Glycosides from Sophora flavescens: Inhibition of the Cytotoxic Effect of d -Galactosamine on Human Hepatocyte HL-7702
inferredcites →https://doi.org/10.1021/np970430bopenalex-snapshot
5-Lipoxygenase and Cyclooxygenase-1 Inhibitory Active Compounds from Atractylodes lancea
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.35.501openalex-snapshot
Gas-liquid chromatographic separation of aldose enantiomers as trimethylsilyl ethers of methyl 2-(polyhydroxyalkyl)-thiazolidine-4(R)-carboxylates.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/cbdv.202200703openalex-snapshot
Sesquiterpenoids Isolated from the Rhizomes of Genus Atractylodes
inferred← citeshttps://doi.org/10.1002/tcr.202100176openalex-snapshot
Polyacetylene Glycosides: Isolation, Biological Activities and Synthesis
inferred← citeshttps://doi.org/10.1007/s11101-026-10230-0openalex-snapshot
Research progress on chemistry, bioactivity, and NMR patterns of acetylene compounds in natural products (2015–2025)
inferred← citeshttps://doi.org/10.1016/j.arabjc.2023.105137openalex-snapshot
Plant polyacetylenoids: Phytochemical, analytical and pharmacological updates
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/j.cclet.2018.09.011openalex-snapshot
Cytotoxic polyacetylenes isolated from the roots and rhizomes of Notopterygium incisum
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e35270openalex-snapshot
Eudesmane-type sesquiterpenoids: Structural diversity and biological activity
inferred← citeshttps://doi.org/10.1016/j.phytol.2018.05.023openalex-snapshot
Four new sesquiterpenes from Atractylodes lancea
inferred← citeshttps://doi.org/10.1039/c9qo01346fopenalex-snapshot
Spiroetherones A and B, sesquiterpene naphthoquinones, as angiogenesis inhibitors from the marine sponge Dysidea etheria
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/10.1186/s13020-026-01473-2openalex-snapshot
A systematic review on the application, phytochemistry and pharmacological activities of the genus Atractylodes
inferred← citeshttps://doi.org/10.2174/0115733947265189231129105327openalex-snapshot
Biological Potential and Therapeutic Effectiveness of a Polyethylene Alkyne Class Phytochemical ‘Atractylodin’ in Medicine for the Treatment of Cancer and other Human Complications
inferred← citeshttps://doi.org/10.3390/metabo13080888openalex-snapshot
Non-Targeted Metabolomics Combined with Chemometrics by UHPLC–Orbitrap–HRMS and Antioxidant Activity of Atractylodes chinensis (DC.) Koidez. from Eight Origins
inferred← citeshttps://doi.org/10.3390/molecules27185753openalex-snapshot
Two Novel Sesquiterpenoid Glycosides from the Rhizomes of Atractylodes lancea
inferred← citeshttps://doi.org/10.4103/pm.pm_33_20openalex-snapshot
Distinguishing the rhizomes of Atractylodes japonica, Atractylodes chinensis, and Atractylodes lancea by comprehensive two-dimensional gas chromatography coupled with mass spectrometry combined with multivariate data analysis
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