On the public citation graph
Artatrovirenols A and B: Two Cagelike Sesquiterpenoids from Artemisia atrovirens
0 signed · 74 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.201601967openalex-snapshot
Artemisinin—A Gift from Traditional Chinese Medicine to the World (Nobel Lecture)
inferredcites →https://doi.org/10.1016/0031-9422(95)00640-0openalex-snapshot
Sesquiterpene lactones with the uncommon rotundane skeleton from Artemisia pontica L.
inferredcites →https://doi.org/10.1016/j.bioorg.2020.103820openalex-snapshot
Seven pairs of new enantiomeric sesquiterpenoids from Curcuma phaeocaulis
inferredcites →https://doi.org/10.1016/j.cbi.2015.08.015openalex-snapshot
Arglabin: From isolation to antitumor evaluation
inferredcites →https://doi.org/10.1016/j.ejphar.2012.10.013openalex-snapshot
Anti-tumor effect of germacrone on human hepatoma cell lines through inducing G2/M cell cycle arrest and promoting apoptosis
inferredcites →https://doi.org/10.1016/j.fitote.2015.11.018openalex-snapshot
Chemical modification of arglabin and biological activity of its new derivatives
inferredcites →https://doi.org/10.1016/j.phytochem.2008.09.022openalex-snapshot
Sesquiterpene lactones from the endemic Cape Verdean Artemisia gorgonum
inferredcites →https://doi.org/10.1016/j.phytochem.2017.11.010openalex-snapshot
The natural sesquiterpene lactones arglabin, grosheimin, agracin, parthenolide, and estafiatin inhibit T cell receptor (TCR) activation
inferredcites →https://doi.org/10.1016/j.phytol.2016.04.017openalex-snapshot
Cytotoxic sesquiterpenoids from Senecio densiserratus
inferredcites →https://doi.org/10.1016/j.phytol.2020.03.009openalex-snapshot
Cytotoxic sesquiterpene lactones from Artemisia myriantha
inferredcites →https://doi.org/10.1016/j.prp.2019.152701openalex-snapshot
Apigenin, a flavonoid constituent derived from P. villosa, inhibits hepatocellular carcinoma cell growth by CyclinD1/CDK4 regulation via p38 MAPK-p21 signaling
inferredcites →https://doi.org/10.1016/j.tetlet.2015.02.100openalex-snapshot
Hemisynthesis of a naturally occurring clinically significant antitumor arglabin from ludartin
inferredcites →https://doi.org/10.1016/j.tetlet.2020.151872openalex-snapshot
Artemilavanolides A and B, two sesquiterpenoids with a 6-oxabicyclo[3.2.1]octane scaffold from Artemisia lavandulaefolia
inferredcites →https://doi.org/10.1021/acs.jnatprod.9b00693openalex-snapshot
Kalshinoids A–F, Anti-inflammatory Sesquiterpenes from Kalimeris shimadae
inferredcites →https://doi.org/10.1021/acs.orglett.7b02681openalex-snapshot
Artemisians A–D, Diseco-guaianolide Involved Heterodimeric [4 + 2] Adducts from Artemisia argyi
inferredcites →https://doi.org/10.1021/acs.orglett.7b03796openalex-snapshot
Dimeric Cadinane Sesquiterpenoid Derivatives from Artemisia annua
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/np0103113openalex-snapshot
Dimeric Guaianolides and a Fulvenoguaianolide from Artemisia myriantha
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/b606168kopenalex-snapshot
Eudesmane sesquiterpenoids from the Asteraceae family
inferredcites →https://doi.org/10.1055/s-2006-957438openalex-snapshot
Biologically Active Substances from the GenusArtemisia
inferredcites →https://doi.org/10.1055/s-2007-967138openalex-snapshot
Willmar Schwabe Award 2006: Antiplasmodial and Antitumor Activity of Artemisinin - From Bench to Bedside
inferredcites →https://doi.org/10.1155/2015/247685openalex-snapshot
Sesquiterpene Lactones fromArtemisiaGenus: Biological Activities and Methods of Analysis
inferredcites →https://doi.org/10.2174/138955711797655399openalex-snapshot
Natural Sesquiterpenoids as Cytotoxic Anticancer Agents
inferredcites →https://doi.org/10.3390/molecules24071209openalex-snapshot
Activity of Estafietin and Analogues on Trypanosoma cruzi and Leishmania braziliensis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/chem.202501468openalex-snapshot
Total Synthesis of Daphnenoid A
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/10.1002/cjoc.202400172openalex-snapshot
Three Types of Isocoumarins with Unusual Carbon Skeletons from Artemisia dubia var. subdigitata and Their Antihepatoma Activity
inferred← citeshttps://doi.org/10.1002/cplu.202500703openalex-snapshot
Formal Total Synthesis of Daphnenoid A
inferred← citeshttps://doi.org/10.1002/ddr.22087openalex-snapshot
Design and synthesis of guaianolide‐germacranolide heterodimers as novel anticancer agents against hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1007/s00044-022-02890-2openalex-snapshot
Design and synthesis of ludartin derivatives as potential anticancer agents against hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1007/s11101-024-09962-8openalex-snapshot
Phytochemical diversity and pharmacological effects of sesquiterpenes from Artemisia spp.
inferred← citeshttps://doi.org/10.1007/s11101-024-09976-2openalex-snapshot
Role of secondary metabolites in plant defense mechanisms: a molecular and biotechnological insights
inferred← citeshttps://doi.org/10.1007/s11101-024-10040-2openalex-snapshot
Unlocking the power of sesquiterpenoids: phytochemistry and bioactivities in Artemisia (2017–2023)
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/10.1007/s13659-022-00340-5openalex-snapshot
Artemyrianosins A–J, cytotoxic germacrane-type sesquiterpene lactones from Artemisia myriantha
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.bioorg.2022.106106openalex-snapshot
A review on natural products with cage-like structure
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106617openalex-snapshot
Design, synthesis, and biological evaluation of artemyrianolide H derivatives as potential antihepatoma agents
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104900openalex-snapshot
Cytotoxic guaianolides and seco-guaianolides from Artemisia atrovirens
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.fitote.2022.105399openalex-snapshot
Artemleucolides A−L, eudesmane-type sesquiterpenoids from Artemisia leucophylla and their antihepatoma cytotoxicity
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105619openalex-snapshot
Artemeriosides A–F, the first examples of natural sesquiterpenoids substituted by a 6′-O-crontonyl β-glucopyranoside from Artemisia annua
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106241openalex-snapshot
Germacrane-type sesquiterpenes from Artemisia atrovirens and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106527openalex-snapshot
Artemiyrianins A-H, guaiane-type sesquiterpenoids from Artemisia myriantha var. pleiocephala and their antihepatoma activity
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.2022.113578openalex-snapshot
Sarcoelegans A–H, eight undescribed cembranes with anti-inflammatory and anti-thrombotic activities from the South China Sea soft coral Sarcophyton elegans
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.2024.114374openalex-snapshot
Artemordosins A−L, cadinane-monoterpene heterodimers and sesquiterpenoids with antihepatoma activity from Artemisia ordosica
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.115040openalex-snapshot
Guaiane sesquiterpenes from Lindera glauca: isolation, structural elucidation, and hepatoprotective effect
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135025openalex-snapshot
Recent advances in total syntheses of cage-like sesquiterpenoids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155113openalex-snapshot
Energetics of proposed cyclizations for the biosynthesis of daphenoid A and artatrovirenols A and B
inferred← citeshttps://doi.org/10.1016/s1875-5364(23)60441-8openalex-snapshot
Artemdubinoids A–N: novel sesquiterpenoids with antihepatoma cytotoxicity from Artemisia dubia
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00267openalex-snapshot
Three Pairs of Enantiomeric Sesquiterpenoids from Syringa pinnatifolia
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03120openalex-snapshot
Biomimetic Synthesis of Lavandiolides H, I, and K and Artematrolide F via Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c04199openalex-snapshot
Routes to Advanced Intermediates in the Synthesis of Tetracarbocyclic Sesquiterpenoids Daphnenoid A and Artatrovirenols A and B
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02322openalex-snapshot
Stelleroids A–C, Three Rearranged Guaiane Sesquiterpenoids with Caged Ring Systems from Stellera chamaejasme
inferred← citeshttps://doi.org/10.1021/jacs.3c09683openalex-snapshot
Enantioselective Total Synthesis of (−)-Artatrovirenol A
inferred← citeshttps://doi.org/10.1021/jacs.5c17555openalex-snapshot
A Concise Total Synthesis of (+)-Pedrolide
inferred← citeshttps://doi.org/10.1038/s41467-024-55560-9openalex-snapshot
Bioinspired concise synthesis of caged Sesquiterpenoids Artatrovirenols A and B
inferred← citeshttps://doi.org/10.1039/d0qo01615bopenalex-snapshot
Trimeric and dimeric sesquiterpenoids from Artemisia atrovirens and their cytotoxicities
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/10.1039/d4nj03909bopenalex-snapshot
Artemdubins A–E from Artemisia dubia var. subdigitata : antihepatoma activity, molecular docking and molecular dynamics studies
inferred← citeshttps://doi.org/10.1039/d4ra01834fopenalex-snapshot
Exploring the synthetic potential of epoxide ring opening reactions toward the synthesis of alkaloids and terpenoids: a review
inferred← citeshttps://doi.org/10.1039/d5sc02952jopenalex-snapshot
Concise total synthesis of the cage-like sesquiterpenoid (+)-daphnepapytone A
inferred← citeshttps://doi.org/10.1080/10286020.2021.2004131openalex-snapshot
Survey of natural products reported by Asian research groups in 2020
inferred← citeshttps://doi.org/10.1080/14786419.2023.2258436openalex-snapshot
Sarcoeleganolides H–K, new anti-thrombotic cembranes from soft coral Sarcophyton elegans
inferred← citeshttps://doi.org/10.3390/jof9040393openalex-snapshot
New Guaiane-Type Sesquiterpenoids Biscogniauxiaols A–G with Anti-Fungal and Anti-Inflammatory Activities from the Endophytic Fungus Biscogniauxia Petrensis
inferred← citeshttps://doi.org/10.3390/md20090574openalex-snapshot
Sarcoeleganolides C–G, Five New Cembranes from the South China Sea Soft Coral Sarcophyton elegans
inferred← citeshttps://doi.org/10.55544/sjmars.3.5.5openalex-snapshot
Secondary Metabolites in Plants: Their Role in Modulating the Immune Response to Viral Infections in Hosts
inferred← citeshttps://doi.org/10.70675/922840cbzcca6z4cdczb2c9zf62f53aa9942openalex-snapshot
Total synthesis of ophiorrhine A, G and ophiorrhiside E and synthetic studies towards the total synthesis of pestalustaine A
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.