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Cytotoxic Germacranolides and Acyclic Diterpenoides from the Seeds of Carpesium triste

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What this work says

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

inferredcites →https://doi.org/10.1016/j.phytochem.2004.03.014openalex-snapshot

Trihydroxylated linear diterpenes from the brown alga Bifurcaria bifurcata

inferredcites →https://doi.org/10.1016/s0021-9673(01)95493-7openalex-snapshot

Separation of geranylgeraniol isomers by high-performance liquid chromatography and identification by 13C nuclear magnetic resonance spectroscopy

inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot

High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

inferredcites →https://doi.org/10.1021/jo00003a068openalex-snapshot

Observation of a transannular Cannizzaro reaction in a caged [7]prismane related system

inferredcites →https://doi.org/10.1021/jo00340a029openalex-snapshot

Germacranolides of Inula eupatorioides. 2. Absolute configuration of the ineupatorolides

inferredcites →https://doi.org/10.1021/jo00340a030openalex-snapshot

Deoxygenation of 7-oxabicyclo[2.2.1]hepta-2,5-diene systems to substituted benzenes by titanium tetrachloride-lithium aluminum hydride

inferredcites →https://doi.org/10.1021/jo01312a007openalex-snapshot

Unusual germacranolides from Inula eupatorioides

inferredcites →https://doi.org/10.1055/s-2002-32899openalex-snapshot

Sesquiterpene Lactone Glycosides, Eudesmanolides, and Other Constituents from Carpesium macrocephalum

inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot

New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Carpesabrolide a, a Succinic Acid-Guaiane Merosesquiterpenoid with Anti-Inflammatory Activity from Carpesium Abrotanoides

inferred← citeshttps://doi.org/10.1002/ange.200903108openalex-snapshot

Die Renaissance der α‐Methylen‐γ‐butyrolactone: neue Syntheseansätze

inferred← citeshttps://doi.org/10.1002/anie.200903108openalex-snapshot

The Renaissance of α‐Methylene‐γ‐butyrolactones: New Synthetic Approaches

inferred← citeshttps://doi.org/10.1002/cbdv.202200898openalex-snapshot

Lipskynoids A–G, New Acyclic Diterpenes from the Flowers ofCarpesium lipskyi

inferred← citeshttps://doi.org/10.1002/ejoc.202300084openalex-snapshot

Discovery of New Cytotoxic Aplaminone Derivatives from the Sea Hare Aplysia kurodai and Elucidation of Their Accumulation from Local Sea Algae through the Food Chain

inferred← citeshttps://doi.org/10.1002/hlca.200890206openalex-snapshot

New Acyclic 12‐Hydroxygeranylgeraniol‐Derived Diterpenoids from the Seeds of Carpesium triste

inferred← citeshttps://doi.org/10.1002/hlca.200900275openalex-snapshot

Diversity of Sesquiterpenoids from Carpesium cernuum

inferred← citeshttps://doi.org/10.1007/s10600-013-0542-zopenalex-snapshot

Sesquiterpenoids from Carpesium lipskyi

inferred← citeshttps://doi.org/10.1007/s10600-015-1383-8openalex-snapshot

A New Sesquiterpenoid from the Flower Buds of Carpesium triste

inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.10.138openalex-snapshot

Antiproliferative and apoptotic sesquiterpene lactones from Carpesium faberi

inferred← citeshttps://doi.org/10.1016/j.fitote.2012.04.016openalex-snapshot

Sesquiterpenoids from Carpesium divaricatum and their cytotoxic activity

inferred← citeshttps://doi.org/10.1016/j.fitote.2018.04.015openalex-snapshot

Sesquiterpenes and diterpenes with cytotoxic activities from the aerial parts of Carpesium humile

inferred← citeshttps://doi.org/10.1016/j.jep.2015.01.027openalex-snapshot

The genus Carpesium: A review of its ethnopharmacology, phytochemistry and pharmacology

inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2011.08.007openalex-snapshot

Diepoxybutane induces the formation of DNA–DNA rather than DNA–protein cross-links, and single-strand breaks and alkali-labile sites in human hepatocyte L02 cells

inferred← citeshttps://doi.org/10.1016/j.mrgentox.2012.06.001openalex-snapshot

DNA damage induced by three major metabolites of 1,3-butadiene in human hepatocyte L02 cells

inferred← citeshttps://doi.org/10.1016/j.phymed.2019.153072openalex-snapshot

Identification of Carpesium cernuum extract as a tumor migration inhibitor based on its biological response profiling in breast cancer cells

inferred← citeshttps://doi.org/10.1016/j.phytol.2018.07.010openalex-snapshot

Three new sesquiterpene lactones from Carpesium abrotanoides

inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.09.067openalex-snapshot

Carpescernolides A and B, rare oxygen bridge-containing sesquiterpene lactones from Carpesium cernuum

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00428openalex-snapshot

Cytotoxic Germacranolides from the Whole Plant of Carpesium minus

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00315openalex-snapshot

Isolation, Structure Elucidation, and Absolute Configuration of Highly Oxygenated Germacranolides from Carpesium cernuum

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b01004openalex-snapshot

Cytotoxic Germacrane-Type Sesquiterpene Lactones from the Whole Plant of Carpesium lipskyi

inferred← citeshttps://doi.org/10.1021/cr2003344openalex-snapshot

Assignment of the Absolute Configuration of Polyfunctional Compounds by NMR Using Chiral Derivatizing Agents

inferred← citeshttps://doi.org/10.1021/np900827aopenalex-snapshot

Humulane and Germacrane Sesquiterpenes from Ferula lycia

inferred← citeshttps://doi.org/10.1021/ol101843qopenalex-snapshot

Convergent Synthesis of TrisubstitutedZ-Allylic Esters by Wittig−Schlosser Reaction

inferred← citeshttps://doi.org/10.1038/s41598-018-30782-2openalex-snapshot

Isolation, Structure Elucidation, and Absolute Configuration of Germacrane Isomers from Carpesium divaricatum

inferred← citeshttps://doi.org/10.1038/srep27237openalex-snapshot

New Highly Oxygenated Germacranolides from Carpesium divaricatum and their Cytotoxic Activity

inferred← citeshttps://doi.org/10.1039/b806216copenalex-snapshot

Natural sesquiterpenoids

inferred← citeshttps://doi.org/10.1039/c9ra00478eopenalex-snapshot

New antiproliferative germacranolides from Carpesium divaricatum

inferred← citeshttps://doi.org/10.1039/d4ra00292jopenalex-snapshot

Carpesabrolide A, a novel meroterpenoid with anti-inflammatory activity from Carpesium abrotanoides

inferred← citeshttps://doi.org/10.1080/14786419.2020.1833199openalex-snapshot

A new highly oxygenated germacranolide from Carpesium nepalense var. lanatum (C.B.Clarke) Kitam

inferred← citeshttps://doi.org/10.1093/jme/tjac009openalex-snapshot

Mosquito Repellent Potential ofCarpesium abrotanoidesEssential Oil and Its Main Components Against a Dengue Vector,Aedes aegypti(Diptera: Culicidae)

inferred← citeshttps://doi.org/10.1111/cbdd.13970openalex-snapshot

An insight into cytotoxic activity of flavonoids and sesquiterpenoids from selected plants of Asteraceae species

inferred← citeshttps://doi.org/10.1177/1934578x1200700704openalex-snapshot

Compounds with Antiproliferative Activity on Five Human Cancer Cell Lines from South Korean Carpesium triste

inferred← citeshttps://doi.org/10.1515/hc-2022-0012openalex-snapshot

Chemical constituents of plants from the genus Carpesium

inferred← citeshttps://doi.org/10.3390/agriculture10070258openalex-snapshot

Light Quality Affects Growth and Physiology of Carpesium triste Maxim. Cultured In Vitro

inferred← citeshttps://doi.org/10.3390/molecules23051078openalex-snapshot

Three New Highly Oxygenated Germacranolides from Carpesium Divaricatum and Their Cytotoxic Activity

inferred← citeshttps://doi.org/10.3390/molecules26154644openalex-snapshot

Germacranolides from Carpesium divaricatum: Some New Data on Cytotoxic and Anti-Inflammatory Activity

inferred← citeshttps://doi.org/10.3390/molecules28020674openalex-snapshot

Feature-Based Molecular Networking for the Exploration of the Metabolome Diversity of Common Egyptian Centaurea Species in Relation to Their Cytotoxic Activity

inferred← citeshttps://doi.org/10.3390/molecules30122506openalex-snapshot

New Terpenoids and Polyphenolic Profile of Carpesium cernuum L. of European Origin

inferred← citeshttps://doi.org/10.3390/plants11212815openalex-snapshot

Chemical Composition and Cytotoxic Activity of Extracts from Carpesium divaricatum: In Vitro- versus Field-Grown Plants

inferred← citeshttps://doi.org/10.3724/sp.j.1009.2010.00104openalex-snapshot

A Germacrane Sesquiterpenoid from Vernonia patula

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