On the public citation graph

Artemisians A–D, Diseco-guaianolide Involved Heterodimeric [4 + 2] Adducts from Artemisia argyi

https://doi.org/10.1021/acs.orglett.7b02681

0 signed · 69 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ange.201409618openalex-snapshot

Total Synthesis and Structural Revision of (+)‐Uprolide G Acetate

inferredcites →https://doi.org/10.1002/anie.201600313openalex-snapshot

Structural Revisions of a Class of Natural Products: Scaffolds of Aglycon Analogues of Fusicoccins and Cotylenins Isolated from Fungi

inferredcites →https://doi.org/10.1002/chem.201502631openalex-snapshot

Involucratustones A–C: Unprecedented Sesquiterpene Dimers Containing Multiple Contiguous Quaternary Carbons from Stahlianthus involucratus

inferredcites →https://doi.org/10.1002/ejoc.201301445openalex-snapshot

Sesquiterpenes from Artemisia argyi: Absolute Configurations and Biological Activities

inferredcites →https://doi.org/10.1016/0031-9422(86)80021-8openalex-snapshot

Seco-guaianolides and other constituents from Artemisia species

inferredcites →https://doi.org/10.1016/j.drudis.2012.01.013openalex-snapshot

Natural and synthetic α-methylenelactones and α-methylenelactams with anticancer potential

inferredcites →https://doi.org/10.1016/j.ejmech.2009.04.029openalex-snapshot

Structure–activity relationship of seco-tanapartholides isolated from Achillea falcata for inhibition of HaCaT cell growth

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.jep.2011.05.040openalex-snapshot

Anti-inflammatory activity of Eupatorium perfoliatum L. extracts, eupafolin, and dimeric guaianolide via iNOS inhibitory activity and modulation of inflammation-related cytokines and chemokines

inferredcites →https://doi.org/10.1016/j.phytochem.2006.01.033openalex-snapshot

Sesquiterpene lactones from Achillea collina J. Becker ex Reichenb.

inferredcites →https://doi.org/10.1016/j.tet.2012.07.057openalex-snapshot

Cytotoxic sesquiterpenes from luminescent mushroom Neonothopanus nambi

inferredcites →https://doi.org/10.1016/j.tetlet.2015.09.127openalex-snapshot

Four new isomeric sesquiterpene lactone dimers from Carpesium faberi

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00953openalex-snapshot

Complementarity of DFT Calculations, NMR Anisotropy, and ECD for the Configurational Analysis of Brevipolides K–O from Hyptis brevipes

inferredcites →https://doi.org/10.1021/acs.orglett.5b02982openalex-snapshot

Polycycloiridals A–D, Four Iridal-Type Triterpenoids with an α-Terpineol Moiety from Iris tectorum

inferredcites →https://doi.org/10.1021/acs.orglett.6b01519openalex-snapshot

Artaboterpenoids A and B, Bisabolene-Derived Sesquiterpenoids from Artabotrys hexapetalus

inferredcites →https://doi.org/10.1021/acs.orglett.6b01944openalex-snapshot

Rhodomyrtials A and B, Two Meroterpenoids with a Triketone-Sesquiterpene-Triketone Skeleton from Rhodomyrtus tomentosa: Structural Elucidation and Biomimetic Synthesis

inferredcites →https://doi.org/10.1021/acs.orglett.7b01276openalex-snapshot

Xylopiana A, a Dimeric Guaiane with a Case-Shaped Core from Xylopia vielana: Structural Elucidation and Biomimetic Conversion

inferredcites →https://doi.org/10.1021/ja0439219openalex-snapshot

Total Synthesis of Absinthin

inferredcites →https://doi.org/10.1021/jo020299zopenalex-snapshot

Arteminolides B, C, and D, New Inhibitors of Farnesyl Protein Transferase from Artemisia argyi

inferredcites →https://doi.org/10.1021/np020593mopenalex-snapshot

Sesquiterpenoids from Artemisia gilvescens and an Anti-MRSA Compound

inferredcites →https://doi.org/10.1021/ol202915ropenalex-snapshot

Bicunningines A and B, Two New Dimeric Diterpenes from Cunninghamia lanceolata

inferredcites →https://doi.org/10.1021/ol501923kopenalex-snapshot

Carpedilactones A–D, Four New Isomeric Sesquiterpene Lactone Dimers with Potent Cytotoxicity from Carpesium faberi

inferredcites →https://doi.org/10.1021/ol800656qopenalex-snapshot

Ainsliadimer A, A New Sesquiterpene Lactone Dimer with an Unusual Carbon Skeleton from Ainsliaea macrocephala

inferredcites →https://doi.org/10.1039/b111251copenalex-snapshot

Diels–Alder and ene reactions of singlet oxygen, nitroso compounds and triazolinediones: transition states and mechanisms from contemporary theory

inferredcites →https://doi.org/10.1039/b305068hopenalex-snapshot

Enzymatic catalysis of the Diels–Alder reaction in the biosynthesis of natural products

inferredcites →https://doi.org/10.1039/c0np00050gopenalex-snapshot

Natural disesquiterpenoids

inferredcites →https://doi.org/10.1039/c6gc02776hopenalex-snapshot

Calcium carbide as the acetylide source: transition-metal-free synthesis of substituted pyrazoles via [1,5]-sigmatropic rearrangements

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.4065292openalex-extracted

inferred← citeshttps://doi.org/10.2139/ssrn.4691606openalex-extracted

Discovery of New Sesquiterpenoids And Jasmonic Acid Derivative From Artemisia Stolonifera And Their Anti-Inflammation Activity

inferred← citeshttps://doi.org/10.1002/cjoc.202100528openalex-snapshot

Artematrovirenolides A—D and Artematrolides S—Z, Sesquiterpenoid Dimers with Cytotoxicity against Three Hepatoma Cell Lines from Artemisia atrovirens

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/10.1007/978-981-99-7329-3_2openalex-snapshot

Classification of Diverse Novel Sesquiterpenoids

inferred← citeshttps://doi.org/10.1007/s11101-020-09698-1openalex-snapshot

Natural disesquiterpenoids: an overview of their chemical structures, pharmacological activities, and biosynthetic pathways

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/s12272-023-01466-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.2018.11.013openalex-snapshot

Artemisianins A-D, new stereoisomers of seco-guaianolide involved heterodimeric [4+2] adducts from Artemisia argyi induce apoptosis via enhancement of endoplasmic reticulum stress

inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105072openalex-snapshot

Artematrovirenins A–P, guaiane-type sesquiterpenoids with cytotoxicities against two hepatoma cell lines from Artemisia atrovirens

inferred← citeshttps://doi.org/10.1016/j.cclet.2026.113281openalex-snapshot

Artemisiverins A–E, three types of architecturally unprecedented sesquiterpenoid dimers from Artemisia sieversiana with antihepatic fibrosis 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.2022.105199openalex-snapshot

Anti-Inflammatory Sesquiterpenoid Dimers from Artemisia Atrovirens

inferred← citeshttps://doi.org/10.1016/j.jep.2022.115658openalex-snapshot

Artemisia argyi extract induces apoptosis in human gemcitabine-resistant lung cancer cells via the PI3K/MAPK signaling pathway

inferred← citeshttps://doi.org/10.1016/j.jff.2018.11.029openalex-snapshot

Phytochemical components and biological activities of Artemisia argyi

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113299openalex-snapshot

Artemidubolides A−T, cytotoxic unreported guaiane-type sesquiterpenoid dimers against three hepatoma cell lines from Artemisia dubia

inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113714openalex-snapshot

Artemiprinolides A−M, thirteen undescribed sesquiterpenoid dimers from Artemisia princeps and their antihepatoma activity

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114120openalex-snapshot

Anti-inflammatory discovery of sesquiterpenoids and a jasmonic acid derivative from Artemisia stolonifera

inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114216openalex-snapshot

Unusual cadinane-involved sesquiterpenoid dimers from Artemisia annua and their antihepatoma effect

inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.115089openalex-snapshot

Artemisiverins A1–A32, structurally diverse guaiane-type sesquiterpenoid dimers from Artemisia sieversiana and their antihepatoma activity

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.phytol.2021.03.011openalex-snapshot

Four new highly oxidized sesquiterpene lactones from the leaves of Artemisia argyi

inferred← citeshttps://doi.org/10.1016/s1875-5364(18)30131-6openalex-snapshot

Advanced natural products chemistry research in China between 2015 and 2017

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00815openalex-snapshot

Taicrypnacids A and B, a Pair of C37 Heterodimeric Diterpenoid Stereoisomers from Taiwania cryptomerioides

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01491openalex-snapshot

Artatrovirenols A and B: Two Cagelike Sesquiterpenoids from Artemisia atrovirens

inferred← citeshttps://doi.org/10.1021/acs.joc.9b01212openalex-snapshot

Echingridimer A, an Oxaspiro Dimeric Sesquiterpenoid with a 6/6/5/6/6 Fused Ring System from Echinops grijsii and Aphicidal Activity Evaluation

inferred← citeshttps://doi.org/10.1038/s41467-018-04487-zopenalex-snapshot

Molecular basis of dimer formation during the biosynthesis of benzofluorene-containing atypical angucyclines

inferred← citeshttps://doi.org/10.1039/c7np90044aopenalex-snapshot

Hot off the press

inferred← citeshttps://doi.org/10.1039/c9cc02681aopenalex-snapshot

Triangeliphthalides A–D: bioactive phthalide trimers with new skeletons from Angelica sinensis and their production mechanism

inferred← citeshttps://doi.org/10.1039/c9np00037bopenalex-snapshot

Naturally occurring [4 + 2] type terpenoid dimers: sources, bioactivities and total syntheses

inferred← citeshttps://doi.org/10.1039/c9np00062copenalex-snapshot

Natural disesquiterpenoids: an update

inferred← citeshttps://doi.org/10.1039/d0qo00960aopenalex-snapshot

Talaronoids A–D: four fusicoccane diterpenoids with an unprecedented tricyclic 5/8/6 ring system from the fungus Talaromyces stipitatus

inferred← citeshttps://doi.org/10.1039/d1qo01404hopenalex-snapshot

Fissisternoids A and B, two 2′,5′-quinodihydrochalcone-based meroterpenoid enantiomers with unusual carbon skeletons from Fissistigma bracteolatum

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/10.1080/14786419.2019.1610754openalex-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/10.3389/fchem.2019.00350openalex-snapshot

Three Pairs of New Spirocyclic Alkaloid Enantiomers From the Marine-Derived Fungus Eurotium sp. SCSIO F452

inferred← citeshttps://doi.org/10.3390/biomedicines11092442openalex-snapshot

Piperlongumine Induces Apoptosis and Cytoprotective Autophagy via the MAPK Signaling Pathway in Human Oral Cancer Cells

inferred← citeshttps://doi.org/10.3390/metabo16060365openalex-snapshot

Untargeted Metabolomics and Metabolite–Gene Network Analysis Predict NF-κB Inhibition in Artemisian B-Treated Triple-Negative Breast Cancer Cells

inferred← citeshttps://doi.org/10.3390/molecules26103038openalex-snapshot

Chemistry and Pharmacological Activity of Sesquiterpenoids from the Chrysanthemum Genus

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.