On the public citation graph
Sesquiterpene Lactones and Thymol Esters from Vicoa pentanema
0 signed · 51 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known work and none has been retracted — and get a dated CiteStamped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/mrc.1260270214openalex-snapshot
Improved 13C1H shift correlation spectra for indirectly bonded carbons and hydrogens: The FLOCK sequence
inferredcites →https://doi.org/10.1016/0031-9422(75)83032-9openalex-snapshot
New sesquiterpene lactones from Liriodendron tulipifera
inferredcites →https://doi.org/10.1016/0031-9422(93)85529-zopenalex-snapshot
Cytotoxic and antibacterial sesquiterpenes from Inula graveolens
inferredcites →https://doi.org/10.1016/0031-9422(95)00807-1openalex-snapshot
Further sesquiterpene lactones from Inula salsoloides
inferredcites →https://doi.org/10.1016/s0031-9422(00)82384-5openalex-snapshot
Guaianolide from Saussurea lappa
inferredcites →https://doi.org/10.1016/s0031-9422(00)98251-7openalex-snapshot
Vicoside A, a 28-nortriterpenoid glucoside from Vicoa indica
inferredcites →https://doi.org/10.1021/jo00442a037openalex-snapshot
Isolation and characterization of peroxyferolide, a hydroperoxy sesquiterpene lactone from Liriodendron tulipifera
inferredcites →https://doi.org/10.1021/np50058a009openalex-snapshot
Chemistry of the Annonaceae, Part XXVI. The Uvarisesquiterpenes, a Novel Type of Benzylated Sesquiterpene from Uvaria angolensis
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.4674500openalex-extracted
Carpesabrolide a, a Succinic Acid-Guaiane Merosesquiterpenoid with Anti-Inflammatory Activity from Carpesium Abrotanoides
inferred← citeshttps://doi.org/10.1002/cbdv.202300220openalex-snapshot
Cytotoxic Terpenes from the Flowers of Inula japonica against Human Hepatocarcinoma Cells
inferred← citeshttps://doi.org/10.1002/hlca.201000417openalex-snapshot
Sesquiterpenoids from the Aerial Parts of Inula japonica
inferred← citeshttps://doi.org/10.1002/pca.900openalex-snapshot
Simultaneous quantification of eudesmanolides and thymol derivatives from tissues of Inula helenium and I. royleana by reversed‐phase high‐performance liquid Chromatography
inferred← citeshttps://doi.org/10.1002/ptr.1258openalex-snapshot
Cytotoxic sesquiterpene lactones from Centaurothamnus maximus and Vicoa pentanema
inferred← citeshttps://doi.org/10.1007/978-981-10-1917-3_9openalex-snapshot
Recent Advances in Asteraceae Tissue Culture
inferred← citeshttps://doi.org/10.1007/s10600-014-0947-3openalex-snapshot
Chemical Constituents of Inula falconeri
inferred← citeshttps://doi.org/10.1007/s10600-015-1529-8openalex-snapshot
Sesquiterpenoids from Cremanthodium potaninii
inferred← citeshttps://doi.org/10.1007/s10600-019-02913-2openalex-snapshot
Chemical Constituents of Inula pterocaula
inferred← citeshttps://doi.org/10.1007/s11101-015-9412-6openalex-snapshot
Systematic evaluation of thymol derivatives possessing stereogenic or prostereogenic centers
inferred← citeshttps://doi.org/10.1007/s12272-013-0143-1openalex-snapshot
Chemical constituents from Inula wissmanniana and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.09.013openalex-snapshot
Sesquiterpenes from Carpesium macrocephalum inhibit Candida albicans biofilm formation and dimorphism
inferred← citeshttps://doi.org/10.1016/j.bse.2012.02.016openalex-snapshot
Terpenoids from Inula sericophylla Franch. and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.chmed.2023.12.006openalex-snapshot
Inula britannica ameliorates alcohol-induced liver injury by modulating SIRT1-AMPK/Nrf2/NF-κB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.08.047openalex-snapshot
Sesquiterpene lactones from Inula falconeri, a plant endemic to the Himalayas, as potential anti-inflammatory agents
inferred← citeshttps://doi.org/10.1016/j.fitote.2005.06.006openalex-snapshot
A new α-methylene γ-lactone sesquiterpene from Hedyosmum arborescens
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.03.015openalex-snapshot
Caroguaianolide A–E, five new cytotoxic sesquiterpene lactones from Carpesium abrotanoides L.
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104292openalex-snapshot
Bioactive sesquiterpenoids and sesquiterpenoid glucosides from the flowers of Inula japonica
inferred← citeshttps://doi.org/10.1016/j.foodchem.2009.10.045openalex-snapshot
Antimicrobial activities of some thymol derivatives from the roots of Inula hupehensis
inferred← citeshttps://doi.org/10.1016/j.jff.2021.104895openalex-snapshot
Electrophilic thymol isobutyrate from Inula nervosa Wall. (Xiaoheiyao) ameliorates steatosis in HepG2 cells via Nrf2 activation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113389openalex-snapshot
Sesquiterpene lactone dimers from the fruit of Carpesium abrotanoides L
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113805openalex-snapshot
Sesquiterpenes from Carpesium faberi triggered ROS-induced apoptosis and protective autophagy in hepatocellular carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.phytol.2009.08.001openalex-snapshot
Two carabrane-type sesquiterpenes from Vladimiria souliei
inferred← citeshttps://doi.org/10.1016/j.phytol.2012.06.012openalex-snapshot
Sesquiterpene lactones from Inula cappa
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.01.025openalex-snapshot
Macrochaetosides A and B, new rare sesquiterpene glycosides from Echinops macrochaetus and their cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.127openalex-snapshot
Four new isomeric sesquiterpene lactone dimers from Carpesium faberi
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c01154openalex-snapshot
High-Content Screening Pipeline for Natural Products Targeting Oncogenic Signaling in Melanoma
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00637openalex-snapshot
Methodology for the Absolute Configuration Determination of Epoxythymols Using the Constituents of Ageratina glabrata
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00371openalex-snapshot
Dicarabrones A and B, a Pair of New Epimers Dimerized from Sesquiterpene Lactones via a [3 + 2] Cycloaddition from Carpesium abrotanoides
inferred← citeshttps://doi.org/10.1021/jf205123dopenalex-snapshot
Synthesis and Antifungal Activities of Carabrol Ester Derivatives
inferred← citeshttps://doi.org/10.1021/np200319xopenalex-snapshot
Pseudoguaianolides and Guaianolides from Inula hupehensis as Potential Anti-inflammatory Agents
inferred← citeshttps://doi.org/10.1039/b606168kopenalex-snapshot
Eudesmane sesquiterpenoids from the Asteraceae family
inferred← citeshttps://doi.org/10.1039/d4ra00292jopenalex-snapshot
Carpesabrolide A, a novel meroterpenoid with anti-inflammatory activity from Carpesium abrotanoides
inferred← citeshttps://doi.org/10.1080/10286020.2011.575066openalex-snapshot
Sesquiterpenoids from Inula racemosa
inferred← citeshttps://doi.org/10.1080/10412905.2010.9700317openalex-snapshot
Volatiles ofTelekia speciosa(Schreb.) Baumg. (Asteraceae) From Serbia
inferred← citeshttps://doi.org/10.1177/1934578x1701201004openalex-snapshot
Further Guaianolides from Chrysophthalmum montanum
inferred← citeshttps://doi.org/10.33263/lianbs124.095openalex-snapshot
Sesquiterpene lactones from Inula confertiflora A. Rich (Asteraceae) Leaf
inferred← citeshttps://doi.org/10.3390/app14188437openalex-snapshot
Allelopathic Activity of Leaf Wastes of Liriodendron tulipifera for Sustainable Management
inferred← citeshttps://doi.org/10.3390/molecules15096485openalex-snapshot
Synthesis and Antifungal Activity of Carabrone Derivatives
inferred← citeshttps://doi.org/10.3390/pathogens8040201openalex-snapshot
Antioxidant and Leishmanicidal Evaluation of Pulicaria Inuloides Root Extracts: A Bioguided Fractionation
inferred← citeshttps://doi.org/10.46793/biolnyss.16.1.22aopenalex-snapshot
Vicoa indica: unveiling the therapeutic properties and phytochemical profiling of a lesser-known medicinal plant
inferred← citeshttps://doi.org/10.5511/plantbiotechnology.24.527openalex-snapshot
Micropropagation and in vitro flowering in Pentanema indicum Ling
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.