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Cytotoxic Flavaglines and Bisamides from Aglaia edulis
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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/(sici)1096-9063(199904)55:4<497::aid-ps946>3.0.co;2-jopenalex-snapshot
Bioactive compounds from neem tissue cultures and screening against insects
inferredcites →https://doi.org/10.1002/ijc.20033openalex-snapshot
Flavaglines: A group of efficient growth inhibitors block cell cycle progression and induce apoptosis in colorectal cancer cells
inferredcites →https://doi.org/10.1007/s007060070023openalex-snapshot
Corrected Structure of Aglalactone Isolated from Aglaia elaeagnoidea (Meliaceae)
inferredcites →https://doi.org/10.1016/0040-4020(96)00322-5openalex-snapshot
New nitrogenous and aromatic derivatives from Aglaia argentea and A. forbesii
inferredcites →https://doi.org/10.1016/j.bmc.2005.09.012openalex-snapshot
Activity-guided isolation of cytotoxic constituents from the bark of Aglaia crassinervia collected in Indonesia
inferredcites →https://doi.org/10.1016/j.phytochem.2005.07.019openalex-snapshot
Phytochemical constituents and hepatoprotective activity of Viburnum tinus
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Cytostatic mechanism and antitumor potential of novel 1H-cyclopenta[b]benzofuran lignans isolated from Aglaiaelliptica
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Insecticidal flavaglines and other compounds from Fijian Aglaia species
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Stress induced carbazole phytoalexins in Glycosmis species
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13C NMR spectral assignment of the A-ring of polyoxygenated flavones
inferredcites →https://doi.org/10.1016/s0031-9422(98)00751-1openalex-snapshot
An insecticidal rocaglamide derivatives and related compounds from Aglaia odorata (Meliaceae)
inferredcites →https://doi.org/10.1016/s0031-9422(99)00185-5openalex-snapshot
Thapsakins: possible biogenetic intermediates towards insecticidal cyclopenta[b]benzofurans from Aglaia edulis
inferredcites →https://doi.org/10.1016/s0031-9422(99)00378-7openalex-snapshot
Bisamides from Aglaia edulis
inferredcites →https://doi.org/10.1016/s0944-7113(96)80067-5openalex-snapshot
Effect of tannins on screening of plant extracts for enzyme inhibitory activity and techniques for their removal
inferredcites →https://doi.org/10.1021/jo040120fopenalex-snapshot
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris
inferredcites →https://doi.org/10.1021/np000123xopenalex-snapshot
New Insecticidal Rocaglamide Derivatives and Related Compounds from Aglaia oligophylla
inferredcites →https://doi.org/10.1021/np000341qopenalex-snapshot
Cytotoxic Constituents from Leaves of Aglaia elliptifolia
inferredcites →https://doi.org/10.1021/np0102354openalex-snapshot
Rocaglamides, Glycosides, and Putrescine Bisamides from Aglaia dasyclada
inferredcites →https://doi.org/10.1021/np0103158openalex-snapshot
Macharistol, a New Cytotoxic Cinnamylphenol from the Stems of Machaerium aristulatum
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Cytotoxic Constituents of the Twigs and Leaves ofAglaiarubiginosa
inferredcites →https://doi.org/10.1021/np50055a010openalex-snapshot
Piriferine, a New Pyrrolidine Alkaloid from Aglaia pirifera Leaves
inferredcites →https://doi.org/10.1021/np50091a005openalex-snapshot
Cytotoxic and Antimalarial Bisbenzylisoquinolme Alkaloids from Stephania erecta
inferredcites →https://doi.org/10.1021/np50094a004openalex-snapshot
Bisamides from Aglaia Species: Structure Analysis and Potential to Reverse Drug Resistance with Cultured Cells
inferredcites →https://doi.org/10.1021/np960346gopenalex-snapshot
Cyclopentabenzofuran Lignan Protein Synthesis Inhibitors from Aglaia odorata
inferredcites →https://doi.org/10.1021/np970163+openalex-snapshot
Cytotoxic and Antiplatelet Aggregation Principles from Aglaia elliptifolia
inferredcites →https://doi.org/10.1021/np9801965openalex-snapshot
Bisamides, Lignans, Triterpenes, and Insecticidal Cyclopenta[b]benzofurans from Aglaia Species
inferredcites →https://doi.org/10.1021/np990454dopenalex-snapshot
Flavonol−Cinnamate Cycloadducts and Diamide Derivatives from Aglaia laxiflora
inferredcites →https://doi.org/10.1021/np990542yopenalex-snapshot
Infraspecific Variation of Sulfur-Containing Bisamides from Aglaia leptantha
inferredcites →https://doi.org/10.1055/s-2001-16471openalex-snapshot
Cytotoxic Cyclopenta[b]benzofuran Derivatives from the Stem Bark of Aglaia formosana
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Cytotoxic Sesquiterpene Lactones Mediate their Death-Inducing Effect in Leukemia T Cells by Triggering Apoptosis
inferredcites →https://doi.org/10.1080/1388020039051744openalex-snapshot
Novel Strategies for the Discovery of Plant-Derived Anticancer Agents
inferredcites →https://doi.org/10.1248/cpb.49.1226openalex-snapshot
Diamide Derivatives and Cycloartanes from the Leaves of Aglaia elliptica.
inferredcites →https://doi.org/10.1351/pac199971091611openalex-snapshot
Novel strategies for the discovery of plant-derived anticancer agents
inferredcites →https://doi.org/10.1515/znc-1999-1-210openalex-snapshot
Structure Activity Relationships of Antiproliferative Rocaglamide Derivatives from Aglaia Species (Meliaceae)
inferredcites →https://doi.org/10.1515/znc-1999-1212openalex-snapshot
1H-Cyclopenta[b]benzofuran Lignans from Aglaia Species Inhibit Cell Proliferation and Alter Cell Cycle Distribution in Human Monocytic Leukemia Cell Lines
inferredcites →https://doi.org/10.2174/1385272013375049openalex-snapshot
Chemistry and Biological Activity of Rocaglamide Derivatives and Related Compounds in Aglaia Species (Meliaceae)
inferredcites →https://doi.org/10.2174/187152006777698123openalex-snapshot
Potential of Cyclopenta[b]benzofurans from Aglaia Species in Cancer Chemotherapy
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Phytochemistry and biological activities of Aglaia species
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A/D-rings-seco limonoids from the fruits of Aglaia edulis and their bioactivities
inferred← citeshttps://doi.org/10.1002/ange.202408610openalex-snapshot
Lewis Acid‐Catalyzed Unusual (4+3) Annulation of para ‐Quinone Methides with Bicyclobutanes: Access to Oxabicyclo[4.1.1]Octanes
inferred← citeshttps://doi.org/10.1002/anie.202408610openalex-snapshot
Lewis Acid‐Catalyzed Unusual (4+3) Annulation of para‐Quinone Methides with Bicyclobutanes: Access to Oxabicyclo[4.1.1]Octanes
inferred← citeshttps://doi.org/10.1002/ejoc.200800661openalex-snapshot
Enantioselective Synthesis of Functionalized 1‐Benzoxepines by Phenoxide Ion Mediated 7‐endo‐tet Carbocyclization of Cyclic Sulfates
inferred← citeshttps://doi.org/10.1002/slct.201601639openalex-snapshot
Ni‐Catalyzed Synthesis of Methylenebisamides: Dual Role of DMSO Both as Methylene Source and Oxidant
inferred← citeshttps://doi.org/10.1002/slct.202303176openalex-snapshot
Synthesis of Benzoxepine Derivatives via Two‐Fold Tandem Metathesis
inferred← citeshttps://doi.org/10.1002/vjch.202400102openalex-snapshot
The genus Aglaia: Diversity in chemical structure and biological activity
inferred← citeshttps://doi.org/10.1007/978-3-319-93506-5_1openalex-snapshot
The Search for Anticancer Agents from Tropical Plants
inferred← citeshttps://doi.org/10.1007/978-3-7091-0748-5_1openalex-snapshot
Chemistry and Biology of Rocaglamides (= Flavaglines) and Related Derivatives from Aglaia Species (Meliaceae)
inferred← citeshttps://doi.org/10.1007/978-94-017-9078-9_14openalex-snapshot
Current and Emerging Therapies Targeting Translation
inferred← citeshttps://doi.org/10.1007/978-94-017-9078-9_5openalex-snapshot
RNA Helicases and Their Cofactors
inferred← citeshttps://doi.org/10.1007/s10600-019-02656-0openalex-snapshot
Chromone Alkaloids: Structural Features, Distribution in Nature, and Biological Activity
inferred← citeshttps://doi.org/10.1007/s11101-021-09761-5openalex-snapshot
Comparative phytochemistry of flavaglines (= rocaglamides), a group of highly bioactive flavolignans from Aglaia species (Meliaceae)
inferred← citeshttps://doi.org/10.1007/s13659-025-00531-wopenalex-snapshot
Nitrogen-containing secondary metabolites from Meliaceae Family and their biological activity: a review
inferred← citeshttps://doi.org/10.1016/bs.alkal.2016.04.001openalex-snapshot
Flavoalkaloids—Isolation, Biological Activity, and Total Synthesis
inferred← citeshttps://doi.org/10.1016/j.bjp.2014.11.009openalex-snapshot
Phytochemicals and antimicrobial potentials of mahogany family
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.10.048openalex-snapshot
Recent advances in the biology and chemistry of the flavaglines
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.ejmech.2015.01.021openalex-snapshot
Bioactive benzofuran derivatives: An insight on lead developments, radioligands and advances of the last decade
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Flavaglines as cross-kingdom translation inhibitors: Heavy halides at C6 potentiate antineoplastic, antiviral, and antifungal activities
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133184openalex-snapshot
A straightforward synthesis of methylenebisamides from amides and DMSO with a substoichiometric amount of (COCl)2
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.141195openalex-snapshot
Steroids and terpenoids from Aglaia edulis and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.141472openalex-snapshot
Iron-catalyzed direct N-methylation of N‑methoxy benzamides: A solvent-free approach to bisamides utilizing the methoxy group as a “build-in” methylene donor
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.10.015openalex-snapshot
Amide-esters from Aglaia tenuicaulis – First representatives of a class of compounds structurally related to bisamides and flavaglines
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113881openalex-snapshot
Anti-cancer bioprospecting on medicinal plants from Indonesia: A review
inferred← citeshttps://doi.org/10.1016/j.phytol.2015.07.003openalex-snapshot
New bisamide compounds from the bark of Aglaia eximia (Meliaceae)
inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.074openalex-snapshot
Constituents of the leaves and stem bark of Aglaia foveolata
inferred← citeshttps://doi.org/10.1016/j.tet.2015.02.028openalex-snapshot
Cytotoxic flavonol-diamide [3+2] adducts from the leaves of Aglaia odorata
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00968openalex-snapshot
Aglatestine A, a Rearranged Limonoid with a 3/6/6 Tricarbocyclic Framework from the Fruits of Aglaia edulis
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Straightforward Entry toward Highly Substituted 2,3-Dihydrobenz[ b ]oxepines by Ring Expansion of Benzopyryliums with Donor–Acceptor Diazo Compounds
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The Relevance of Higher Plants in Lead Compound Discovery Programs
inferred← citeshttps://doi.org/10.1039/c4np00006dopenalex-snapshot
Rocaglamide, silvestrol and structurally related bioactive compounds from Aglaia species
inferred← citeshttps://doi.org/10.1039/c4ra14948copenalex-snapshot
A convenient synthesis of 2-substituted benzofurans from salicylaldehydes
inferred← citeshttps://doi.org/10.1039/c7np00064bopenalex-snapshot
The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research
inferred← citeshttps://doi.org/10.1039/d1sc04180kopenalex-snapshot
Silacyclization through palladium-catalyzed intermolecular silicon-based C(sp 2 )–C(sp 3 ) cross-coupling
inferred← citeshttps://doi.org/10.1039/d2qo01070dopenalex-snapshot
Gold( i )-catalyzed diastereo- and enantioselective [4 + 3] cycloadditions: construction of functionalized furano-benzoxepins
inferred← citeshttps://doi.org/10.1039/d3ob00170aopenalex-snapshot
Rh( iii )-catalyzed (5 + 2)-cycloaddition reactions of ortho -hydroxyethyl phenols with internal alkynes: efficient synthesis of benzoxepines
inferred← citeshttps://doi.org/10.1039/d4cc05911eopenalex-snapshot
NBS-mediated C(sp 3 )–H amidation of N,N -dimethylamides with N -acyloxyamides
inferred← citeshttps://doi.org/10.1172/jci34753openalex-snapshot
Therapeutic suppression of translation initiation modulates chemosensitivity in a mouse lymphoma model
inferred← citeshttps://doi.org/10.1177/1934578x1601101115openalex-snapshot
Substrate Specificity of Aglaia loheri Active Isolate towards P-glycoprotein in Multidrug-Resistant Cancer Cells
inferred← citeshttps://doi.org/10.1186/1472-6882-13-286openalex-snapshot
A phenolic ester from Aglaia loheri leaves reveals cytotoxicity towards sensitive and multidrug-resistant cancer cells
inferred← citeshttps://doi.org/10.1360/ssc-2025-0149openalex-snapshot
Progress in the study of non-limonoid natural products of the Meliaceae family
inferred← citeshttps://doi.org/10.20884/1.jm.2022.17.1.5594openalex-snapshot
Terpenoids from the Stem bark of Aglaia elaeagnoidea and their cytotoxic activity against HeLa and DU145 Cancer Cell lines
inferred← citeshttps://doi.org/10.2174/0122103155287599240226061517openalex-snapshot
Terpenoid Components from Branches and Leaves of Aglaia lawii and their Biological Properties
inferred← citeshttps://doi.org/10.31557/apjcp.2021.22.1.53openalex-snapshot
Cytotoxic and Apoptotic Activity of Aglaforbesin Derivative Isolated from Aglaia loheri Merr. on HCT116 Human Colorectal Cancer Cells
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Chemoselective Dual Functionalization of Phenols via Relay Catalysis of Borane with Different Forms
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