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Cytotoxic and Anti-inflammatory Triterpenoids from Toona ciliata
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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/chem.200700663openalex-snapshot
Xylogranatins F–R: Antifeedants from the Chinese Mangrove, Xylocarpus granatum, A New Biogenetic Pathway to Tetranortriterpenoids
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Tirucallane-type triterpenoids: nmr and X-ray diffraction analyses of 24-epi-piscidinol A and piscidinol A
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Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
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Limonoids and protolimonoids from the fruits of Phellodendron amurense
inferredcites →https://doi.org/10.1016/0031-9422(94)00851-jopenalex-snapshot
Triterpenoids from Walsura piscidia
inferredcites →https://doi.org/10.1016/0305-1978(94)90107-4openalex-snapshot
Limonoids from Toona ciliata and speculations on their chemosystematic and ecological significance
inferredcites →https://doi.org/10.1016/j.phytochem.2004.06.019openalex-snapshot
Limonoids from Turraea floribunda (Meliaceae)
inferredcites →https://doi.org/10.1016/j.tet.2007.04.078openalex-snapshot
Tabularisins A–D, phragmalin ortho esters with new skeleton isolated from the seeds of Chukrasia tabularis
inferredcites →https://doi.org/10.1016/j.tet.2007.05.107openalex-snapshot
Eight new limonoids from Turraea pubescens
inferredcites →https://doi.org/10.1016/j.tet.2009.07.023openalex-snapshot
Cipadonoids B–G, six new limonoids from Cipadessa cinerascens
inferredcites →https://doi.org/10.1016/s0031-9422(00)83040-xopenalex-snapshot
Triterpenoids from walsura piscidia
inferredcites →https://doi.org/10.1021/ja00339a031openalex-snapshot
Additivity relation in the amplitudes of exciton-split circular dichroism curves arising from interactions between different chromophores and its application in structural studies
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Stereochemistry of Isoplagiochin C, A Macrocyclic Bisbibenzyl from Liverworts
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Constituents of Trichilia hispida (Meliaceae). 2. A new triterpenoid, hispidone, and bourjotinolone A
inferredcites →https://doi.org/10.1021/jo048631popenalex-snapshot
Saludimerines A and B, Novel-Type Dimeric Alkaloids with Stereogenic Centers and Configurationally Semistable Biaryl Axes
inferredcites →https://doi.org/10.1021/np100599gopenalex-snapshot
Triterpenoids from Aglaia abbreviata and Their Cytotoxic Activities
inferredcites →https://doi.org/10.1021/np990607xopenalex-snapshot
Tetranortriterpenoids from Walsura yunnanensis
inferredcites →https://doi.org/10.1021/ol062101topenalex-snapshot
Xylogranatins A−D: Novel Tetranortriterpenoids with an Unusual 9,10-seco Scaffold from Marine Mangrove Xylocarpus granatum
inferredcites →https://doi.org/10.1021/ol800415nopenalex-snapshot
Cipadonoid A, a Novel Limonoid with an Unprecedented Skeleton, from Cipadessa cinerasecns
inferredcites →https://doi.org/10.1055/s-2000-9901openalex-snapshot
Phytochemical Investigation of Aglaia andamanica
inferredcites →https://doi.org/10.1248/bpb.29.191openalex-snapshot
Limonoids: Overview of Significant Bioactive Triterpenes Distributed in Plants Kingdom
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Cytotoxic Quassinoids and Tirucallane-Type Triterpenes from the Woods of Eurycoma longifolia.
inferredcites →https://doi.org/10.2174/1385272003375941openalex-snapshot
The Chemistry of the Meliaceae and Ptaeroxylaceae of Southern and Eastern Africa and Madagascar
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112661zenodo-depositor-declared
Toonaones A−I, limonoids with NLRP3 inflammasome inhibitory activity from Toona ciliata M. Roem
inferred← citeshttps://doi.org/10.1002/mrc.5229openalex-snapshot
Triterpenes and limonoids of Cedrela : Distribution, biosynthesis, and 1 H and 13 C NMR data
inferred← citeshttps://doi.org/10.1007/s10600-013-0784-9openalex-snapshot
Chemical Constituents of the Rhizomes of Alpinia oxyphylla
inferred← citeshttps://doi.org/10.1007/s11101-018-9557-1openalex-snapshot
Cedrela and Toona genera: a rich source of bioactive limonoids and triterpenoids
inferred← citeshttps://doi.org/10.1007/s13659-020-00274-wopenalex-snapshot
Four New Limonoids from the Barks of Toona ciliata
inferred← citeshttps://doi.org/10.1007/s13659-026-00631-1openalex-snapshot
Distribution and bioactivities of tirucallane-type triterpenoids from Meliaceae family
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Novel C-17 spirost protostane-type triterpenoids from Alisma plantago-aquatica with anti-inflammatory activity in Caco-2 cells
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104363openalex-snapshot
Toonaolides A–X, limonoids from Toona ciliata: Isolation, structural elucidation, and bioactivity against NLRP3 inflammasome
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105817openalex-snapshot
Natural terpenoids with anti-inflammatory activities: Potential leads for anti-inflammatory drug discovery
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inferred← citeshttps://doi.org/10.1016/j.bse.2025.105200openalex-snapshot
Limonoid- and tirucallane-type triterpenoids from the twigs and leaves of Toona ciliata (Meliaceae) and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.fitote.2012.09.009openalex-snapshot
Sesquiterpenes from the aerial part of Chloranthus japonicus and their cytotoxicities
inferred← citeshttps://doi.org/10.1016/j.fitote.2013.04.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fitote.2013.08.015openalex-snapshot
Labdane diterpenes from Chloranthus serratus
inferred← citeshttps://doi.org/10.1016/j.fitote.2015.08.007openalex-snapshot
Anti-inflammatory tirucallane triterpenoids from Anopyxis klaineana Pierre (Engl.), (Rhizophoraceae)
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104838openalex-snapshot
Stigmastane-type steroid saponins from the leaves of Vernonia amygdalina Del
inferred← citeshttps://doi.org/10.1016/j.fitote.2025.106962openalex-snapshot
Toonasonoids A-K, limonoids from Toona ciliata M. Roem, attenuate inflammatory response through mediating the PI3K/AKT/NF-κB pathway
inferred← citeshttps://doi.org/10.1016/j.indcrop.2021.113533openalex-snapshot
The bioactive limonoids from Toona ciliate as NLRP3 inflammasome inhibitors
inferred← citeshttps://doi.org/10.1016/j.jchromb.2015.11.015openalex-snapshot
Separation and characterization of bufadienolides in toad skin using two-dimensional normal-phase liquid chromatography × reversed-phase liquid chromatography coupled with mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.jtcme.2023.05.004openalex-snapshot
Antimalarial activity of Toona ciliata MJ Roem aqueous methanolic leaf extract and its antioxidant and phytochemical properties
inferred← citeshttps://doi.org/10.1016/j.phytochem.2013.10.002openalex-snapshot
Monoterpene indole alkaloids from the stem bark of Mitragyna diversifolia and their acetylcholine esterase inhibitory effects
inferred← citeshttps://doi.org/10.1016/j.phytochem.2014.05.019openalex-snapshot
Phytotoxic cis-clerodane diterpenoids from the Chinese liverwort Scapania stephanii
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112596openalex-snapshot
Tirucallane triterpenoids from the mastic (Pistacia lentiscus) and their anti-inflammatory and cytotoxic activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113276openalex-snapshot
Chemical constituents of Entandrophragma angolense and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113870openalex-snapshot
Lanostane triterpenoids from mycelia-associated Ganoderma sinense and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.phytol.2018.01.020openalex-snapshot
Furan fragment isomerized mexicanolide-type Limonoids from the stem barks of Khaya senegalensis
inferred← citeshttps://doi.org/10.1016/j.steroids.2014.04.014openalex-snapshot
Cytotoxic steroids from the leaves of Dysoxylum binectariferum
inferred← citeshttps://doi.org/10.1016/j.steroids.2021.108831openalex-snapshot
Arthriniumsteroids A–D, four new steroids from the soft coral-derived fungus Simplicillium lanosoniveum SCSIO41212
inferred← citeshttps://doi.org/10.1016/j.tet.2015.09.025openalex-snapshot
B-seco-29-nor-Limonoids from the stem barks of Toona ciliate var. yunnanensis
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134169openalex-snapshot
Limonoids, triterpenes, sterols, and flavonoids from Cedrela odorata L. and their cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.tet.2025.135032openalex-snapshot
Ciliatones M-U: Characterization of limonoid constituents from Toona ciliata
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.02.057openalex-snapshot
An unusual 9,11-seco limonoid from Toona ciliata
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154254openalex-snapshot
Tociliatonoid A: A novel limonoid from Toona ciliata
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Determination of the absolute configuration of natural products
inferred← citeshttps://doi.org/10.1016/s1875-5364(25)60844-2openalex-snapshot
Bioactive triterpenoids from the tuber of Alisma orientale
inferred← citeshttps://doi.org/10.1021/acs.jafc.6c06602openalex-snapshot
Bioactive Terpenoids and Steroids from Astragalus complanatus Seeds underlie Its Potent Neuroprotective Efficacy In Vitro and In Vivo
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00321openalex-snapshot
Protostane Triterpenoids from the Rhizome of Alisma orientale Exhibit Inhibitory Effects on Human Carboxylesterase 2
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00442openalex-snapshot
Limonoids with 11β-Hydroxysteroid Dehydrogenase Type 1 Inhibitory Activities from Dysoxylum mollissimum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01137openalex-snapshot
Cytotoxic Tirucallane and Apotirucallane Triterpenoids from the Stems of Picrasma quassioides
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00208openalex-snapshot
Structurally Diverse Highly Oxygenated Triterpenoids from the Roots of Ailanthus altissima and Their Cytotoxicity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00954openalex-snapshot
Cytotoxic Limonoids from the Twigs and Leaves of Toona ciliata
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00580openalex-snapshot
Antcamphorols A–K, Cytotoxic and ROS Scavenging Triterpenoids from Antrodia camphorata
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03227openalex-snapshot
Leonuketal, a Spiroketal Diterpenoid from Leonurus japonicus
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00738openalex-snapshot
Spirotrichilins A and B: Two Rearranged Spirocyclic Limonoids from Trichilia connaroides
inferred← citeshttps://doi.org/10.1021/np300428ropenalex-snapshot
(±)-Tylopilusins, Diphenolic Metabolites from the Fruiting Bodies of Tylopilus eximius
inferred← citeshttps://doi.org/10.1021/np400276qopenalex-snapshot
Bioactive Limonoid and Triterpenoid Constituents of Turraea pubescens
inferred← citeshttps://doi.org/10.1021/np400700gopenalex-snapshot
Cytotoxic Dammarane-Type Triterpenoids from the Stem Bark of Dysoxylum binecteriferum
inferred← citeshttps://doi.org/10.1021/np400797sopenalex-snapshot
A,D-seco-Limonoids from the Stems of Clausena emarginata
inferred← citeshttps://doi.org/10.1039/c5ra15982bopenalex-snapshot
Penchinones A–D, two pairs of cis-trans isomers with rearranged neolignane carbon skeletons from Penthorum chinense
inferred← citeshttps://doi.org/10.1080/00032719.2017.1327536openalex-snapshot
Fragmentation Study of Limonoids from Turraae pubescens by Electrospray Ionization Quadrupole Time-of-flight Mass Spectrometry
inferred← citeshttps://doi.org/10.1080/10286020.2016.1193491openalex-snapshot
Limonoids with neuroprotective activity from the stems of Clausena emarginata
inferred← citeshttps://doi.org/10.1080/14786419.2018.1553879openalex-snapshot
Antileishmanial and cytotoxic activities of a new limonoid and a new phenyl alkene from the stem bark of Trichilia gilgiana (Meliaceae)
inferred← citeshttps://doi.org/10.1080/14786419.2019.1627351openalex-snapshot
Toonamicrocarpavarin, a new tirucallane-type triterpenoid from Toona Ciliata
inferred← citeshttps://doi.org/10.1080/14786419.2024.2429115openalex-snapshot
Discovery of two new tirucallane-type triterpenes anomers from Toona ciliata
inferred← citeshttps://doi.org/10.1177/1534735414547110openalex-snapshot
Date Palm Pollen as a Preventative Intervention in Radiation- and Chemotherapy-Induced Oral Mucositis
inferred← citeshttps://doi.org/10.1177/1934578x1501000107openalex-snapshot
Phytotoxicity of Triterpenes and Limonoids from the Rutaceae and Meliaceae. 5α,6β,8α,12α-Tetrahydro-28-norisotoonafolin – a Potent Phytotoxin from Toona ciliata
inferred← citeshttps://doi.org/10.12677/br.2026.153015openalex-snapshot
Research Progress on Toona ciliata Germplasm Resources
inferred← citeshttps://doi.org/10.1371/journal.pone.0111049openalex-snapshot
In Silico Assay Development for Screening of Tetracyclic Triterpenoids as Anticancer Agents against Human Breast Cancer Cell Line MCF7
inferred← citeshttps://doi.org/10.2174/1385272827666221017141255openalex-snapshot
Isolation and Bioactivities of Limonoids from Meliaceae Family: A Review
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-2bpb9-v2openalex-snapshot
Chemistry and Biology of Novel Meliaceae Limonoids
inferred← citeshttps://doi.org/10.26434/chemrxiv-2022-2bpb9-v3openalex-snapshot
Chemistry and Biology of Novel Meliaceae Limonoids
inferred← citeshttps://doi.org/10.3109/1547691x.2012.732121openalex-snapshot
Extracts ofFicus exasperataleaf inhibit topical and systemic inflammation in rodents and suppress LPS-induced expression of mediators of inflammation in macrophages
inferred← citeshttps://doi.org/10.3390/md16120488openalex-snapshot
Mangrove Tirucallane- and Apotirucallane-Type Triterpenoids: Structure Diversity of the C-17 Side-Chain and Natural Agonists of Human Farnesoid/Pregnane–X–Receptor
inferred← citeshttps://doi.org/10.3390/molecules25040801openalex-snapshot
Two New Apotirucallane-Type Triterpenoids from the Pericarp of Toona sinensis and Their Ability to Reduce Oxidative Stress in Rat Glomerular Mesangial Cells Cultured under High-Glucose Conditions
inferred← citeshttps://doi.org/10.3390/molecules27020435openalex-snapshot
The Untargeted Phytochemical Profile of Three Meliaceae Species Related to In Vitro Cytotoxicity and Anti-Virulence Activity against MRSA Isolates
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