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Bisamides, Lignans, Triterpenes, and Insecticidal Cyclopenta[b]benzofurans from Aglaia Species
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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/mrc.1260311203openalex-snapshot
Complete 1H (600 MHz) and 13C NMR spectral assignments of 3,4‐bis [(3,4‐dimethoxyphenyl)‐methyl]dihydro‐(3R‐trans)‐2(3H)‐furanone (matairesinol dimethyl ether), a naturally occurring dibenzylbutyrolactone lignan
inferredcites →https://doi.org/10.1007/978-3-642-49187-0openalex-snapshot
Dünnschicht-Chromatographie
inferredcites →https://doi.org/10.1016/0031-9422(82)85208-4openalex-snapshot
Structure and stereochemistry of (−)-odorinol, an antileukemic diamide from Aglaia odorata
inferredcites →https://doi.org/10.1016/0031-9422(93)80052-topenalex-snapshot
Two glabretal-type triterpenoids from the heartwood of Aglaia ferruginaea
inferredcites →https://doi.org/10.1016/0031-9422(95)00415-4openalex-snapshot
Tirucallane triterpenes from the stem bark of Aglaia leucophylla
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(96)00322-5openalex-snapshot
New nitrogenous and aromatic derivatives from Aglaia argentea and A. forbesii
inferredcites →https://doi.org/10.1016/0305-1978(94)90002-7openalex-snapshot
Insecticidal bioactivity of crude extracts of Aglaia species (meliaceae)
inferredcites →https://doi.org/10.1016/s0031-9422(00)94986-0openalex-snapshot
Insecticidal 1H-cyclopentatetrahydro[b]benzofurans from Aglaia odorata
inferredcites →https://doi.org/10.1016/s0031-9422(96)00763-7openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia duppereana
inferredcites →https://doi.org/10.1016/s0031-9422(97)00145-3openalex-snapshot
Pregnanes and triterpenoid hydroperoxides from the leaves of Aglaia grandis
inferredcites →https://doi.org/10.1016/s0031-9422(97)00253-7openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia elliptica and A. harmsiana
inferredcites →https://doi.org/10.1016/s0031-9422(97)00689-4openalex-snapshot
A revision of the structure of ferrugin from Aglaia ferruginaea
inferredcites →https://doi.org/10.1016/s0040-4020(01)97360-0openalex-snapshot
Triterpenoid constituents of thai medicinal plants—II
inferredcites →https://doi.org/10.1021/ja00180a082openalex-snapshot
Diazirinyl anion: a cyclic 4.pi.-electron system
inferredcites →https://doi.org/10.1021/jo00051a050openalex-snapshot
Anti-tumor agents. 136. Cumingianosides A-F, potent antileukemic new triterpene glucosides, and cumindysosides A and B, trisnor- and tetranortriterpene glucosides with a 14,18-cycloapoeuphane-type skeleton from Dysoxylum cumingianum
inferredcites →https://doi.org/10.1021/np50055a010openalex-snapshot
Piriferine, a New Pyrrolidine Alkaloid from Aglaia pirifera Leaves
inferredcites →https://doi.org/10.1021/np50068a044openalex-snapshot
Roxburghiadiol A and Roxburghiadiol B, Two 14α-Methylsterols from Aglaia roxburghiana
inferredcites →https://doi.org/10.1021/np50078a023openalex-snapshot
Justiciresinol, a New Furanoid Lignan from Justicia glauca
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/np50121a030openalex-snapshot
Cycloartane Triterpenes from the Leaves of Aglaia harmsiana
inferredcites →https://doi.org/10.1021/np960159iopenalex-snapshot
Apotirucallane Triterpenes from Aglaia argentea
inferredcites →https://doi.org/10.1021/np960346gopenalex-snapshot
Cyclopentabenzofuran Lignan Protein Synthesis Inhibitors from Aglaia odorata
inferredcites →https://doi.org/10.1021/np9604238openalex-snapshot
Bioactive Amides from Glycosmis species
inferredcites →https://doi.org/10.1021/np960594copenalex-snapshot
Argenteanones C−E and Argenteanols B−E, Cytotoxic Cycloartanes from Aglaia argentea
inferredcites →https://doi.org/10.1055/s-2006-962328openalex-snapshot
New Cycloartenol Derivatives fromAglaia roxburghiana1
inferredcites →https://doi.org/10.1055/s-2006-962695openalex-snapshot
Antiviral Activity of (+)-Odorinol1
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/10.3897/pharmacia.70.e111111zenodo-depositor-declared
Isolation and activity test of antioxidant, antibacterial, and cytotoxic compounds from the stem bark of Aglaia foveolata Pannell
inferred← citeshttps://doi.org/10.1002/9781118231838.ch6openalex-snapshot
Plant Biodiversity as a Resource for Natural Products for Insect Pest Management
inferred← citeshttps://doi.org/10.1002/9783527684403.ch7openalex-snapshot
Bioactive Flavaglines: Synthesis and Pharmacology
inferred← citeshttps://doi.org/10.1002/ange.201608937openalex-snapshot
(C6F5)3B Catalyzed Chemoselective and ortho‐Selective Substitution of Phenols with α‐Aryl α‐Diazoesters
inferred← citeshttps://doi.org/10.1002/anie.201608937openalex-snapshot
(C6F5)3B Catalyzed Chemoselective and ortho‐Selective Substitution of Phenols with α‐Aryl α‐Diazoesters
inferred← citeshttps://doi.org/10.1002/cbdv.202101008openalex-snapshot
Three New Aglain Derivatives from Aglaia odorata Lour. and Their Cytotoxic Activities
inferred← citeshttps://doi.org/10.1002/chem.201303385openalex-snapshot
Catalytic and Asymmetric Fluorolactonisations of Carboxylic Acids through Anion Phase Transfer
inferred← citeshttps://doi.org/10.1002/hlca.200590236openalex-snapshot
Dolabellane Diterpenoids from the Higher Plant Aglaia odorata
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/ijc.20033openalex-snapshot
Flavaglines: A group of efficient growth inhibitors block cell cycle progression and induce apoptosis in colorectal cancer cells
inferred← citeshttps://doi.org/10.1002/jccs.201800320openalex-snapshot
Synthesis of tetrahydrobenzo[b]furans via a gold(I)‐catalyzed rearrangement/cycloisomerization sequence of cyclic 1‐aryl‐2‐propargyl‐cyclohex‐2enols
inferred← citeshttps://doi.org/10.1002/vjch.202400102openalex-snapshot
The genus Aglaia: Diversity in chemical structure and biological activity
inferred← citeshttps://doi.org/10.1007/978-3-540-46907-0_10openalex-snapshot
Plant Natural Products as a Source for Developing Environmentally Acceptable Insecticides
inferred← citeshttps://doi.org/10.1007/978-3-540-74543-3_10openalex-snapshot
Constitutive Secondary Plant Metabolites and Soil Fungi: Defense Against or Facilitation of Diversity
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/10.1007/978-3-7091-6331-3_2openalex-snapshot
Sulfur-Containing Amides from Glycosmis Species (Rutaceae)
inferred← citeshttps://doi.org/10.1007/978-81-322-2006-0_15openalex-snapshot
Phytochemical Pesticides
inferred← citeshttps://doi.org/10.1007/s00432-003-0461-7openalex-snapshot
Naturally occurring lignans efficiently induce apoptosis in colorectal tumor cells
inferred← citeshttps://doi.org/10.1007/s00508-006-0683-1openalex-snapshot
Development of a pharmacodynamic screening model with Crithidia fasciculata
inferred← citeshttps://doi.org/10.1007/s00508-007-0874-4openalex-snapshot
Development of a pharmacodynamic screening model with Entamoeba histolytica
inferred← citeshttps://doi.org/10.1007/s10600-014-0936-6openalex-snapshot
Chemical Constituents of Aglaia abbreviata
inferred← citeshttps://doi.org/10.1007/s11101-019-09602-6openalex-snapshot
Structural classification and biological activities of Stemona alkaloids
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/s11738-011-0923-5openalex-snapshot
Physiological and cellular mechanisms of natural herbicide resource from Aglaia odorata Lour. on bioassay plants
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/b978-0-12-819304-4.00003-8openalex-snapshot
Pesticides, History, and Classification
inferred← citeshttps://doi.org/10.1016/b978-0-444-64058-1.00009-1openalex-snapshot
Amides From Plants: Structures and Biological Importance
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.bmcl.2006.09.084openalex-snapshot
Ponapensin, a cyclopenta[bc]benzopyran with potent NF-κB inhibitory activity from Aglaia ponapensis
inferred← citeshttps://doi.org/10.1016/j.bse.2004.05.005openalex-snapshot
Rocaglamide, aglain, and other related derivatives from Aglaia testicularis (Meliaceae)
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.2013.04.011openalex-snapshot
Limonoids from the West African Trichilia welwitschii (Meliaceae)
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.ejmech.2026.119394openalex-snapshot
Flavaglines as cross-kingdom translation inhibitors: Heavy halides at C6 potentiate antineoplastic, antiviral, and antifungal activities
inferred← citeshttps://doi.org/10.1016/j.fitote.2012.05.003openalex-snapshot
Molluscicidal activity of Aglaia duperreana and the constituents of its twigs and leaves
inferred← citeshttps://doi.org/10.1016/j.phytochem.2007.06.016openalex-snapshot
Flavaglines and triterpenoids from the leaves of Aglaia forbesii
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.2008.08.025openalex-snapshot
Silvaglins and related 2,3-secodammarane derivatives – unusual types of triterpenes from Aglaia silvestris
inferred← citeshttps://doi.org/10.1016/j.phytochem.2010.03.005openalex-snapshot
Dolabellane diterpenoids from Aglaia odorata
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.tet.2007.05.074openalex-snapshot
Constituents of the leaves and stem bark of Aglaia foveolata
inferred← citeshttps://doi.org/10.1016/j.toxicon.2004.05.007openalex-snapshot
Lignoids in insects: chemical probes for the study of ecdysis, excretion and Trypanosoma cruzi—triatomine interactions
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00205-3openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia spectabilis (Meliaceae)
inferred← citeshttps://doi.org/10.1016/s0031-9422(00)00471-4openalex-snapshot
Insecticidal flavaglines and other compounds from Fijian Aglaia species
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00185-5openalex-snapshot
Thapsakins: possible biogenetic intermediates towards insecticidal cyclopenta[b]benzofurans from Aglaia edulis
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00378-7openalex-snapshot
Bisamides from Aglaia edulis
inferred← citeshttps://doi.org/10.1016/s0031-9422(99)00519-1openalex-snapshot
Three putrescine bisamides from the leaves of Aglaia grandis
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01180-2openalex-snapshot
New methoxylated aryltetrahydronaphthalene lignans and a norlignan from Aglaia cordata
inferred← citeshttps://doi.org/10.1016/s0099-9598(02)58003-2openalex-snapshot
Putrescine, spermidine, spermine, and related polyamine alkaloids
inferred← citeshttps://doi.org/10.1021/acs.jafc.2c03011openalex-snapshot
Oxidosqualene Cyclases Involved in the Biosynthesis of Diverse Triterpenes in Camellia sasanqua
inferred← citeshttps://doi.org/10.1021/ja503163kopenalex-snapshot
Highly Site-Selective Direct C–H Bond Functionalization of Phenols with α-Aryl-α-diazoacetates and Diazooxindoles via Gold Catalysis
inferred← citeshttps://doi.org/10.1021/jf990509hopenalex-snapshot
Cyclopenta[b]benzofurans from Aglaia Species with Pronounced Antifungal Activity against Rice Blast Fungus (Pyricularia grisea)
inferred← citeshttps://doi.org/10.1021/jo040120fopenalex-snapshot
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris
inferred← citeshttps://doi.org/10.1021/jo051299copenalex-snapshot
Synthesis of 2,3-Disubstituted Benzo[b]furans by the Palladium-Catalyzed Coupling ofo-Iodoanisoles and Terminal Alkynes, Followed by Electrophilic Cyclization
inferred← citeshttps://doi.org/10.1021/np000123xopenalex-snapshot
New Insecticidal Rocaglamide Derivatives and Related Compounds from Aglaia oligophylla
inferred← citeshttps://doi.org/10.1021/np0102354openalex-snapshot
Rocaglamides, Glycosides, and Putrescine Bisamides from Aglaia dasyclada
inferred← citeshttps://doi.org/10.1021/np0102962openalex-snapshot
Aglacins A−D, First Representatives of a New Class of Aryltetralin Cyclic Ether Lignans fromAglaiacordata
inferred← citeshttps://doi.org/10.1021/np020291kopenalex-snapshot
Cyclorocaglamide, the First Bridged Cyclopentatetrahydrobenzofuran, and a Related “Open Chain” Rocaglamide Derivative from Aglaia oligophylla
inferred← citeshttps://doi.org/10.1021/np0304417openalex-snapshot
Cytotoxic Constituents of the Twigs and Leaves ofAglaiarubiginosa
inferred← citeshttps://doi.org/10.1021/np060428xopenalex-snapshot
Cytotoxic Flavaglines and Bisamides from Aglaia edulis
inferred← citeshttps://doi.org/10.1021/np070184wopenalex-snapshot
Putrescine Bisamides from Aglaia gigantea
inferred← citeshttps://doi.org/10.1021/np990013uopenalex-snapshot
Cytotoxic 3,4-Secoapotirucallanes from Aglaia argentea Bark
inferred← citeshttps://doi.org/10.1021/np990242gopenalex-snapshot
New Insecticidal Rocaglamide Derivatives from the Roots of Aglaia duperreana
inferred← citeshttps://doi.org/10.1021/np990542yopenalex-snapshot
Infraspecific Variation of Sulfur-Containing Bisamides from Aglaia leptantha
inferred← citeshttps://doi.org/10.1021/np9905923openalex-snapshot
Phytochemical Investigation of Aglaia rubiginosa
inferred← citeshttps://doi.org/10.1021/ol050805hopenalex-snapshot
Compound Representatives of a New Type of Triterpenoid from Aglaia odorata
inferred← citeshttps://doi.org/10.1039/b505491eopenalex-snapshot
Iodo- and bromo-enolcyclization of 2-(2-propenyl)cyclohexanediones and 2-(2-propenyl)cyclohexenone derivatives using iodine in methanol and pyridinium hydrobromide perbromide in dichloromethane
inferred← citeshttps://doi.org/10.1039/c3cc47350copenalex-snapshot
Synthesis of dihydrobenzo[b]furans by diastereoselective acyloxyarylation
inferred← citeshttps://doi.org/10.1039/c4np00006dopenalex-snapshot
Rocaglamide, silvestrol and structurally related bioactive compounds from Aglaia species
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/c8ob02161aopenalex-snapshot
Preparation of polysubstituted dihydrofurans through a PhI(OAc) 2 -promoted haloenolcyclization of olefinic dicarbonyl compounds
inferred← citeshttps://doi.org/10.1074/jbc.m208003200openalex-snapshot
Rocaglamide Derivatives Are Potent Inhibitors of NF-κB Activation in T-cells
inferred← citeshttps://doi.org/10.1079/pavsnnr20094049openalex-snapshot
Comparing impacts of plant extracts and pure allelochemicals and implications for pest control.
inferred← citeshttps://doi.org/10.1080/10286020.2020.1776704openalex-snapshot
Cytotoxic triterpenoids from the stem bark of Aglaia angustifolia
inferred← citeshttps://doi.org/10.1080/10286020.2025.2564409openalex-snapshot
Cytotoxic cycloartane-type triterpenoids from the leaves of aglaia shawiana
inferred← citeshttps://doi.org/10.1080/10286020008039904openalex-snapshot
Note: Synthesis of (+)-Lariciresinol 3a-Acetate, A Lignan fromAglaia elaeagnoidea
inferred← citeshttps://doi.org/10.1080/10286020903565226openalex-snapshot
Chemical constituents from the leaves of Aglaia perviridis
inferred← citeshttps://doi.org/10.1080/14786419.2010.508038openalex-snapshot
Biologically active constituents ofAglaia erythrosperma
inferred← citeshttps://doi.org/10.1080/14786419.2010.511219openalex-snapshot
Aglaianine, a new bisamide fromAglaia abbreviata
inferred← citeshttps://doi.org/10.1080/14786419.2016.1160233openalex-snapshot
A New (–)-5′,6-dimethoxyisolariciresinol-(3″,4″-dimethoxy)-3α-O-β- D -glucopyranoside from the bark of Aglaia eximia (Meliaceae)
inferred← citeshttps://doi.org/10.1080/14786419.2021.1893723openalex-snapshot
Chemical constituents of Aglaia elaeagnoidea and Aglaia odorata and their cytotoxicity
inferred← citeshttps://doi.org/10.1080/14786419.2022.2162514openalex-snapshot
Phenolic and bisamide derivatives from Aglaia odorata and their biological activities
inferred← citeshttps://doi.org/10.1080/14786419.2025.2476204openalex-snapshot
A new nemoralisin-type diterpenoid from Aglaia lawii
inferred← citeshttps://doi.org/10.1107/s1600536810034227openalex-snapshot
Absolute configuration of odorine
inferred← citeshttps://doi.org/10.1139/v10-085openalex-snapshot
Terpenoid constituents and antifungal activity of Aglaia forbesii seed against phytopathogens
inferred← citeshttps://doi.org/10.11588/heidok.00013237openalex-snapshot
Molecular mechanisms of anti-proliferative effects of the Traditional Chinese Medicinal compound Rocaglamide A on cancers
inferred← citeshttps://doi.org/10.11648/j.jps.20140201.16openalex-snapshot
Bioantifungal Activity of Selected Medicinal Plant Extracts against Root Rot of Fungal Disease
inferred← citeshttps://doi.org/10.1177/1934578x1100600316openalex-snapshot
Identification and Quantitative Determination of Lignans in Cedrus atlantica Resins using 13 C NMR Spectroscopy
inferred← citeshttps://doi.org/10.1248/cpb.49.1226openalex-snapshot
Diamide Derivatives and Cycloartanes from the Leaves of Aglaia elliptica.
inferred← citeshttps://doi.org/10.12982/cmujns.2017.0024openalex-snapshot
Cytotoxic Steroids from the Bark of Aglaia argentea (Meliaceae)
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/10.1515/znb-2021-0060openalex-snapshot
Antimycobacterial cycloartane derivatives from the roots of Trichilia welwistchii C. DC (Meliaceae)
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/10.20884/1.jm.2023.18.3.7824openalex-snapshot
Steroids Produced by Endophytic Fungus Lasiodiplodia Theobromae From Aglaia Argentea Blume and Their Cytotoxic Activity Against Hela Cervical Cancer Cell Lines
inferred← citeshttps://doi.org/10.31635/ccschem.020.202000404openalex-snapshot
Chemoselective Dual Functionalization of Phenols via Relay Catalysis of Borane with Different Forms
inferred← citeshttps://doi.org/10.32508/stdjns.v5i3.1035openalex-snapshot
Chemical constituents of Aglaia odorata and Aglaia hoaensis
inferred← citeshttps://doi.org/10.3390/molecules200916566openalex-snapshot
Benzofuranyl Esters: Synthesis, Crystal Structure Determination, Antimicrobial and Antioxidant Activities
inferred← citeshttps://doi.org/10.3732/ajb.92.3.534openalex-snapshot
Aglaia (Meliaceae): an evaluation of taxonomic concepts based on DNA data and secondary metabolites
inferred← citeshttps://doi.org/10.4172/2161-0444.1000167openalex-snapshot
Synthesis of Putrescine Bisamides as Antimicrobial and Anti-Inflammatory Agents
inferred← citeshttps://doi.org/10.4269/ajtmh.19-0350openalex-snapshot
Vismione B Interferes with Trypanosoma cruzi Infection of Vero Cells and Human Stem Cell–Derived Cardiomyocytes
inferred← citeshttps://doi.org/10.5012/bkcs.2010.31.04.965openalex-snapshot
Facile Preparation of 2-Arylbenzo[b]furan Molecules and Their Anti-inflammatory Effects
inferred← citeshttps://doi.org/10.5012/bkcs.2012.33.6.1907openalex-snapshot
Ailanthoidol Derivatives and their Anti-inflammatory Effects
inferred← citeshttps://doi.org/10.70675/7d68b550za64ez450ez9652z105c70164939openalex-snapshot
Development of new approaches for the synthesis of flavaglines
inferred← citeshttps://doi.org/10.7454/mss.v19i1.4476openalex-snapshot
Flavonoid Compounds from the Bark of Aglaia eximia (Meliaceae)
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