On the public citation graph
Cytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis
0 signed · 78 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200702707openalex-snapshot
Enantioselective Synthesis of the Complex Rocaglate (−)‐Silvestrol
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.2011.10.048openalex-snapshot
Recent advances in the biology and chemistry of the flavaglines
inferredcites →https://doi.org/10.1016/j.tet.2007.05.074openalex-snapshot
Constituents of the leaves and stem bark of Aglaia foveolata
inferredcites →https://doi.org/10.1016/j.tet.2015.02.028openalex-snapshot
Cytotoxic flavonol-diamide [3+2] adducts from the leaves of Aglaia odorata
inferredcites →https://doi.org/10.1016/s0009-2797(98)00073-8openalex-snapshot
Cytostatic mechanism and antitumor potential of novel 1H-cyclopenta[b]benzofuran lignans isolated from Aglaiaelliptica
inferredcites →https://doi.org/10.1016/s0031-9422(00)00205-3openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia spectabilis (Meliaceae)
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(98)00279-9openalex-snapshot
Chlorosis-inducing products from Pseudomonas syringae pathovars: new N-coronafacoyl compounds
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/s1470-2045(08)70209-2openalex-snapshot
Targeted manipulation of apoptosis in cancer treatment
inferredcites →https://doi.org/10.1021/cr9904009openalex-snapshot
Quantum Mechanical Continuum Solvation Models
inferredcites →https://doi.org/10.1021/ja300900popenalex-snapshot
Formal Synthesis of (±)-Methyl Rocaglate Using an Unprecedented Acetyl Bromide Mediated Nazarov Reaction
inferredcites →https://doi.org/10.1021/ja808402eopenalex-snapshot
Total Synthesis of the Potent Anticancer Aglaia Metabolites (−)-Silvestrol and (−)-Episilvestrol and the Active Analogue (−)-4′-Desmethoxyepisilvestrol
inferredcites →https://doi.org/10.1021/ja9029736openalex-snapshot
Nazarov Cyclization Initiated by Peracid Oxidation: The Total Synthesis of (±)-Rocaglamide
inferredcites →https://doi.org/10.1021/jo040120fopenalex-snapshot
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris
inferredcites →https://doi.org/10.1021/jo202366copenalex-snapshot
Total Synthesis of (±)-Rocaglamide via Oxidation-Initiated Nazarov Cyclization
inferredcites →https://doi.org/10.1021/np300376fopenalex-snapshot
Total Synthesis of 2‴,5‴-Diepisilvestrol and Its C1‴ Epimer: Key Structure Activity Relationships at C1‴ and C2‴
inferredcites →https://doi.org/10.1021/np3005425openalex-snapshot
Cytotoxic Alkaloids from the Whole Plants of Zephyranthes candida
inferredcites →https://doi.org/10.1021/np3007588openalex-snapshot
Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis
inferredcites →https://doi.org/10.1021/np5000507openalex-snapshot
Diterpenoids from the Chinese Liverwort Heteroscyphus tener and Their Antiproliferative Effects
inferredcites →https://doi.org/10.1021/np960346gopenalex-snapshot
Cyclopentabenzofuran Lignan Protein Synthesis Inhibitors from Aglaia odorata
inferredcites →https://doi.org/10.1039/b515476fopenalex-snapshot
Application of electronic circular dichroism in configurational and conformational analysis of organic compounds
inferredcites →https://doi.org/10.1039/c4np00006dopenalex-snapshot
Rocaglamide, silvestrol and structurally related bioactive compounds from Aglaia species
inferredcites →https://doi.org/10.1080/10286020801948367openalex-snapshot
Two new pregnanes fromAglaia perviridisHiern
inferredcites →https://doi.org/10.1080/10286020903565226openalex-snapshot
Chemical constituents from the leaves of Aglaia perviridis
inferredcites →https://doi.org/10.1107/s0021889808042726openalex-snapshot
OLEX2 : a complete structure solution, refinement and analysis program
inferredcites →https://doi.org/10.1126/science.1238303openalex-snapshot
Tight Coordination of Protein Translation and HSF1 Activation Supports the Anabolic Malignant State
inferredcites →https://doi.org/10.1158/1535-7163.mct-06-0564openalex-snapshot
Docetaxel-induced apoptosis in melanoma cells is dependent on activation of caspase-2
inferredcites →https://doi.org/10.1172/jci34753openalex-snapshot
Therapeutic suppression of translation initiation modulates chemosensitivity in a mouse lymphoma model
inferredcites →https://doi.org/10.1182/blood-2008-09-175430openalex-snapshot
The novel plant-derived agent silvestrol has B-cell selective activity in chronic lymphocytic leukemia and acute lymphoblastic leukemia in vitro and in vivo
inferredcites →https://doi.org/10.1371/journal.pone.0005223openalex-snapshot
Antitumor Activity and Mechanism of Action of the Cyclopenta[b]benzofuran, Silvestrol
inferredcites →https://doi.org/10.1371/journal.pone.0076136openalex-snapshot
Therapeutic Potential of the Translation Inhibitor Silvestrol in Hepatocellular Cancer
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/10.2174/1566524033479483openalex-snapshot
The Role of Apoptosis in Tumor Progression and Metastasis
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.
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/ange.201707539openalex-snapshot
Total Syntheses of the Isomeric Aglain Natural Products Foveoglin A and Perviridisin B: Selective Excited‐State Intramolecular Proton‐Transfer Photocycloaddition
inferred← citeshttps://doi.org/10.1002/anie.201707539openalex-snapshot
Total Syntheses of the Isomeric Aglain Natural Products Foveoglin A and Perviridisin B: Selective Excited‐State Intramolecular Proton‐Transfer Photocycloaddition
inferred← citeshttps://doi.org/10.1002/ardp.202200367openalex-snapshot
Synthetic flavagline derivative 1‐chloroacetylrocaglaol promotes apoptosis in K562 erythroleukemia cells through miR‐17‐92 cluster genes
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/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/j.antiviral.2024.105976openalex-snapshot
Amidino-rocaglates (ADRs), a class of synthetic rocaglates, are potent inhibitors of SARS-CoV-2 replication through inhibition of viral protein synthesis
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104667openalex-snapshot
Toonasindiynes A-F, new polyacetylenes from Toona sinensis with cytotoxic and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114298openalex-snapshot
Flavaglines with anti-neuroinflammatory activity from Aglaia edulis (Roxb.) Wall. and structure revision of related flavaglines
inferred← citeshttps://doi.org/10.1016/j.phytol.2023.08.001openalex-snapshot
A new limonoid with immunosuppressive activity from Munronia pinnata
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131257openalex-snapshot
Anti-inflammatory flavagline glycosides and putrescine bisamides from Aglaia perviridis leaves
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00036openalex-snapshot
Discovery of Anticancer Agents of Diverse Natural Origin
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01247openalex-snapshot
Additional Bioactive Silvestrol Analogs from the Roots of Aglaia perviridis Collected in Vietnam
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00631openalex-snapshot
Structurally Modified Cyclopenta[b]benzofuran Analogues Isolated from Aglaia perviridis
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02308openalex-snapshot
Characteristic Flavaglines with Therapeutic Potential for Ischemic Stroke from Aglaia perviridis
inferred← citeshttps://doi.org/10.1021/acs.oprd.8b00213openalex-snapshot
Light on the Horizon: Current Research and Future Perspectives in Flow Photochemistry
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02173openalex-snapshot
Walrobsins A and B, Two Anti-inflammatory Limonoids from Root Barks of Walsura robusta
inferred← citeshttps://doi.org/10.1038/s41598-018-37666-5openalex-snapshot
Oxo-aglaiastatin-Mediated Inhibition of Translation Initiation
inferred← citeshttps://doi.org/10.1055/a-1401-9562openalex-snapshot
Update on Phytochemical and Biological Studies on Rocaglate Derivatives from Aglaia Species
inferred← citeshttps://doi.org/10.1080/14786419.2022.2114472openalex-snapshot
New dammarane-type triterpenoids from Aglaia elliptica (C.DC.) blume
inferred← citeshttps://doi.org/10.1128/mbio.03329-19openalex-snapshot
Translation Inhibition by Rocaglates Activates a Species-Specific Cell Death Program in the Emerging Fungal Pathogen Candida auris
inferred← citeshttps://doi.org/10.13057/biodiv/d220918openalex-snapshot
Fractions and isolated compounds from Lansium domesticum fruit peel exhibited cytotoxic activity against T-47D and HepG2 cell lines
inferred← citeshttps://doi.org/10.14499/indonesianjcanchemoprev9iss3pp143-151openalex-snapshot
Cytotoxic Activity of Ethyl Acetate Fraction of Aglaia elliptica Blume Leaves Extract on HepG2 Hepatocarcinoma 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.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.2023.18.3.7900openalex-snapshot
The Sesquiterpenoids from Aglaia cucullata Peel Fruit and Their Cytotoxic Activities Against B16-F10 and HeLa Cancer Cell Lines
inferred← citeshttps://doi.org/10.22146/ijc.64502openalex-snapshot
Phytochemistry and Pharmacology of Munronia Genus (Meliaceae)
inferred← citeshttps://doi.org/10.22146/ijc.83694openalex-snapshot
Cytotoxic Dammarane-Type Triterpenoids from Aglaia cucullata Peel Fruit
inferred← citeshttps://doi.org/10.25135/rnp.395.2304.2756openalex-snapshot
NO Inhibitory, Farnesoid X Receptor, and Cytotoxic Activities of Phytochemical Composition Isolated from Aglaia perviridis
inferred← citeshttps://doi.org/10.31080/asms.2020.04.0748openalex-snapshot
An Update on Natural Occurrence and Biological Activity of Benzofurans
inferred← citeshttps://doi.org/10.3389/fchem.2018.00045openalex-snapshot
Natural Products Research in China From 2015 to 2016
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/molecules27248758openalex-snapshot
Phytochemistry and Biological Activities of Guarea Genus (Meliaceae)
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/10.3390/su151813565openalex-snapshot
Cytotoxic Evaluation and Elucidation of Dammarane-Type Triterpenoids Isolated from the Exocarp of Aglaia cucullata (Meliaceae)
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.