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Triterpenoids from Aglaia abbreviata and Their Cytotoxic Activities
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00567286openalex-snapshot
A new triterpene from the leaves ofBetula mandschurica
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/0031-9422(95)00765-2openalex-snapshot
Antibacterial hydroperoxysterols from Xanthosoma robustum
inferredcites →https://doi.org/10.1016/0031-9422(96)00130-6openalex-snapshot
Triterpenoids, lignans and a benzofuran derivative from the bark of Aglaia elaeagnoidea
inferredcites →https://doi.org/10.1016/0040-4020(75)80042-1openalex-snapshot
Cabralea eichleriana dc. (meliaceae)—I structure and stereochemistry of wood extractives
inferredcites →https://doi.org/10.1016/j.bse.2008.03.009openalex-snapshot
Flavaglines and triterpenes as chemical markers of Aglaia oligophylla
inferredcites →https://doi.org/10.1016/j.phytochem.2007.06.016openalex-snapshot
Flavaglines and triterpenoids from the leaves of Aglaia forbesii
inferredcites →https://doi.org/10.1016/j.phytochem.2008.08.025openalex-snapshot
Silvaglins and related 2,3-secodammarane derivatives – unusual types of triterpenes from Aglaia silvestris
inferredcites →https://doi.org/10.1016/s0031-9422(00)00471-4openalex-snapshot
Insecticidal flavaglines and other compounds from Fijian Aglaia species
inferredcites →https://doi.org/10.1016/s0031-9422(00)81537-xopenalex-snapshot
Deacetoxybrachycarpone, a trinortriterpenoid from Cleome brachycarpa
inferredcites →https://doi.org/10.1016/s0031-9422(99)00053-9openalex-snapshot
Dammarane triterpenes and pregnane steroids from Aglaia lawii and A. tomentosa
inferredcites →https://doi.org/10.1016/s0378-8741(99)00063-xopenalex-snapshot
Anti-inflammatory activity of Aglaia roxburghiana var. beddomei extract and triterpenes roxburghiadiol A and B
inferredcites →https://doi.org/10.1021/jf990509hopenalex-snapshot
Cyclopenta[b]benzofurans from Aglaia Species with Pronounced Antifungal Activity against Rice Blast Fungus (Pyricularia grisea)
inferredcites →https://doi.org/10.1021/jo040120fopenalex-snapshot
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris
inferredcites →https://doi.org/10.1021/np0304417openalex-snapshot
Cytotoxic Constituents of the Twigs and Leaves ofAglaiarubiginosa
inferredcites →https://doi.org/10.1039/p19770000510openalex-snapshot
Triterpenoids of Aglaia odorata. Configuration of trisubstituted epoxides
inferredcites →https://doi.org/10.1055/s-2006-962695openalex-snapshot
Antiviral Activity of (+)-Odorinol1
inferredcites →https://doi.org/10.1248/cpb.52.153openalex-snapshot
3-Epicabraleahydroxylactone and Other Triterpenoids from Camellia Oil and Their Inhibitory Effects on Epstein-Barr Virus Activation
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.2020.112540zenodo-depositor-declared
Phytochemistry and biological activities of Aglaia species
inferred← citeshttps://doi.org/10.1002/hlca.201500228openalex-snapshot
Four New Pregnane Steroids from Aglaia abbreviata and Their Cytotoxic Activities
inferred← citeshttps://doi.org/10.1002/vjch.202400102openalex-snapshot
The genus Aglaia: Diversity in chemical structure and biological activity
inferred← citeshttps://doi.org/10.1007/s00289-020-03221-4openalex-snapshot
Studies of chemical and mechanical properties of hybrid composites based on natural resin Dammar formulated by epoxy resin
inferred← citeshttps://doi.org/10.1007/s10600-014-0936-6openalex-snapshot
Chemical Constituents of Aglaia abbreviata
inferred← citeshttps://doi.org/10.1007/s10600-016-1665-9openalex-snapshot
A New Triterpeniod from Aglaia perviridis
inferred← citeshttps://doi.org/10.1007/s13659-025-00553-4openalex-snapshot
First discovery of triterpenoids and sterols from Cotinus coggygria var. cinereus Engl. with anti-inflammatory and antibacterial activities
inferred← citeshttps://doi.org/10.1016/b978-0-444-59603-1.00001-1openalex-snapshot
Recent Insights into the Emerging Role of Triterpenoids in Cancer Therapy
inferred← citeshttps://doi.org/10.1016/b978-0-444-63294-4.00001-2openalex-snapshot
Recent Insights into the Emerging Role of Triterpenoids in Cancer Therapy
inferred← citeshttps://doi.org/10.1016/j.bse.2011.12.022openalex-snapshot
Chemical constituents from Aglaia odorata Lour
inferred← citeshttps://doi.org/10.1016/j.bse.2022.104427openalex-snapshot
Terpenoids from the twigs and leaves of Aglaia elaeagnoidea and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.bse.2023.104668openalex-snapshot
Phytochemical investigation on the leaves of Ailanthus altissima (Mill.) Swingle
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2019.03.020openalex-snapshot
Hydroperoxy steroids and triterpenoids derived from plant and fungi: Origin, structures and biological activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113792openalex-snapshot
Undescribed 2,9-deoxyflavonoids and flavonol-diamide [3+2] adduct from the leaves of Aglaia odorata Lour. Inhibit nitric oxide production
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114297openalex-snapshot
Triterpenoids from Frankincense and Boswellia: A focus on their pharmacology and 13C-NMR assignments
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114439openalex-snapshot
Structurally diverse dammarane-derived triterpenoids from the twigs of Aglaia perviridis Hiern and their α-glucosidase and PTP1B inhibitory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.115098openalex-snapshot
Structural diversity of bioactive triterpenoids from Alangium salviifolium and their attenuation of acute lung injury through AKT/MAPK signaling
inferred← citeshttps://doi.org/10.1016/j.phytol.2012.04.013openalex-snapshot
Cytotoxic triterpenoids from the bark of Aglaia smithii (Meliaceae)
inferred← citeshttps://doi.org/10.1016/j.phytol.2014.01.005openalex-snapshot
Cytotoxic constituents from the bark of Aglaia eximia (Meliaceae)
inferred← citeshttps://doi.org/10.1016/j.phytol.2017.07.006openalex-snapshot
New cytotoxic protolimonoids from the stem bark of Aglaia argentea (Meliaceae)
inferred← citeshttps://doi.org/10.1016/j.steroids.2021.108902openalex-snapshot
Dammarane triterpenes and phytosterols from Dysoxylum tpongense Pierre and their anti-inflammatory activity against liver X receptors and NF-κB activation
inferred← citeshttps://doi.org/10.1016/j.tet.2022.133042openalex-snapshot
Triterpenoids from Chios mastic gum of Pistacia lentiscus and their inhibition of LPS-induced NO production in RAW 264.7 cells
inferred← citeshttps://doi.org/10.1016/s1875-5364(12)60001-6openalex-snapshot
Natural products chemistry research 2010's progress in China
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00493openalex-snapshot
Asymmetric Construction of Remote Vicinal Quaternary and Tertiary Stereocenters via Direct Doubly Vinylogous Michael Addition
inferred← citeshttps://doi.org/10.1021/np200579bopenalex-snapshot
Cytotoxic and Anti-inflammatory Triterpenoids from Toona ciliata
inferred← citeshttps://doi.org/10.1039/c3ra43344gopenalex-snapshot
Highly enantioselective direct vinylogous Michael addition of γ-substituted deconjugated butenolides to maleimides catalyzed by chiral squaramides
inferred← citeshttps://doi.org/10.1039/c5ra23626fopenalex-snapshot
Phytosteroids and triterpenoids with potent cytotoxicities from the leaves of Chisocheton cumingianus
inferred← citeshttps://doi.org/10.1039/c7cc01763dopenalex-snapshot
An asymmetric vinylogous Mukaiyama–Michael reaction of α,β-unsaturated 2-acyl imidazoles catalyzed by chiral Sc( iii )– or Er( iii )–pybox complexes
inferred← citeshttps://doi.org/10.1039/d1cc00777gopenalex-snapshot
Catalytic asymmetric coupling of vinylogous species via deconjugated butenolide addition to vinylogous imines in situ generated from arylsulfonyl indoles
inferred← citeshttps://doi.org/10.1039/d4ob01175aopenalex-snapshot
A quinine-squaramide catalyzed enantioselective vinylogous Mannich reaction between benzothiazolimines and γ-butenolides for efficient preparation of chiral N -benzothiazole butyrolactones
inferred← citeshttps://doi.org/10.1080/14786419.2022.2114472openalex-snapshot
New dammarane-type triterpenoids from Aglaia elliptica (C.DC.) blume
inferred← citeshttps://doi.org/10.1107/s1600536812040366openalex-snapshot
3-epi-Dammarenediol II 1.075 hydrate: a dammarane triterpene from the bark ofAglaia eximia
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/10.1248/cpb.c16-00868openalex-snapshot
Aglaiabbrevins A–D, New Prenylated Bibenzyls from the Leaves of Aglaia abbreviata with Potent PTP1B Inhibitory Activity
inferred← citeshttps://doi.org/10.12982/cmujns.2017.0024openalex-snapshot
Cytotoxic Steroids from the Bark of Aglaia argentea (Meliaceae)
inferred← citeshttps://doi.org/10.13005/ojc/350114openalex-snapshot
Triterpenoids from the Bark of Aglaia glabrata and their In vitro Effects on P-388 Murine Leukemia Cells
inferred← citeshttps://doi.org/10.18632/oncotarget.17287openalex-snapshot
Triterpenoids fromAglaia abbreviataexert cytotoxicity and multidrug resistant reversal effect in MCF-7/ADM cells via reactive oxygen species induction and P-glycoprotein inhibition
inferred← citeshttps://doi.org/10.20307/nps.2017.23.4.291openalex-snapshot
Cytotoxicity and Structure Activity Relationship of Dammarane-Type Triterpenoids from the Bark of Aglaia elliptica against P-388 Murine Leukemia Cells
inferred← citeshttps://doi.org/10.20884/1.jm.2017.12.2.361openalex-snapshot
A Cytotoxic Rocaglate Compound from The Stembark of Aglaia argentea (Meliaceae)
inferred← citeshttps://doi.org/10.20884/1.jm.2019.14.2.543openalex-snapshot
Caryophyllene-Type Sesquiterpenoids from the Stembark of Aglalia harmsiana and Their Cytotoxic Activity Against MCF-7 Breast Cancer Cells
inferred← citeshttps://doi.org/10.3390/ijms24021252openalex-snapshot
New 3,4-seco-3,19-Dinor- and Spongian-Based Diterpenoid Lactones from the Marine Sponge Spongia sp.
inferred← citeshttps://doi.org/10.3390/molecules27196757openalex-snapshot
Dammarane-Type Triterpenoid from the Stem Bark of Aglaia elliptica (Meliaceae) and Its Cytotoxic Activities
inferred← citeshttps://doi.org/10.3390/molecules28134946openalex-snapshot
The Cytotoxic Activity of Dammarane-Type Triterpenoids Isolated from the Stem Bark of Aglaia cucullata (Meliaceae)
inferred← citeshttps://doi.org/10.4314/ijbcs.v11i1.39openalex-snapshot
Détermination structurale de triterpenoïdes isolés des feuilles de Combretum glutinosium Perr. Ex DC (Combretaceae)
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