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New Insecticidal Rocaglamide Derivatives and Related Compounds from Aglaia oligophylla
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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/10.1016/0040-4020(96)00322-5openalex-snapshot
New nitrogenous and aromatic derivatives from Aglaia argentea and A. forbesii
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)00253-7openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia elliptica and A. harmsiana
inferredcites →https://doi.org/10.1016/s0031-9422(98)00751-1openalex-snapshot
An insecticidal rocaglamide derivatives and related compounds from Aglaia odorata (Meliaceae)
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Thapsakins: possible biogenetic intermediates towards insecticidal cyclopenta[b]benzofurans from Aglaia edulis
inferredcites →https://doi.org/10.1016/s0031-9422(99)00327-1openalex-snapshot
New insecticidal rocaglamide derivatives from flowers of Aglaia duperreana (Meliaceae)
inferredcites →https://doi.org/10.1021/ja00180a082openalex-snapshot
Diazirinyl anion: a cyclic 4.pi.-electron system
inferredcites →https://doi.org/10.1021/np50055a010openalex-snapshot
Piriferine, a New Pyrrolidine Alkaloid from Aglaia pirifera Leaves
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/np990242gopenalex-snapshot
New Insecticidal Rocaglamide Derivatives from the Roots of Aglaia duperreana
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/adsc.200600570openalex-snapshot
Asymmetric Total Synthesis of Nigerone and ent‐Nigerone: Enantioselective Oxidative Biaryl Coupling of Highly Hindered Naphthols
inferred← citeshttps://doi.org/10.1002/arch.70028openalex-snapshot
Stimulation of IRES‐Dependent Translation by Rocaglamide A Increases the Replication and Virulence of Cricket Paralysis Virus in Lepidopteran Insect Cells
inferred← citeshttps://doi.org/10.1002/chir.20557openalex-snapshot
The online assignment of the absolute configuration of natural products: HPLC‐CD in combination with quantum chemical CD calculations
inferred← citeshttps://doi.org/10.1002/ejoc.200700905openalex-snapshot
Total Synthesis and Biological Activity of (±)‐Rocaglamide and Its 2,3‐Di‐epi Analogue
inferred← citeshttps://doi.org/10.1002/ijc.22883openalex-snapshot
The traditional Chinese herbal compound rocaglamide preferentially induces apoptosis in leukemia cells by modulation of mitogen‐activated protein kinase activities
inferred← citeshttps://doi.org/10.1002/jcc.1084openalex-snapshot
MD‐based CD calculations for the assignment of the absolute axial configuration of the naphthylisoquinoline alkaloid dioncophylline A
inferred← citeshttps://doi.org/10.1002/vjch.202400102openalex-snapshot
The genus Aglaia: Diversity in chemical structure and biological activity
inferred← citeshttps://doi.org/10.1007/978-3-642-55519-0_4openalex-snapshot
Full Absolute Stereostructures of Natural Products Directly from Crude Extracts: The HPLC-MS/MS-NMR-CD ‘Triad’
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/10.1007/978-3-7091-6227-9_1openalex-snapshot
Biaryls in Nature: A Multi-Facetted Class of Stereochemically, Biosynthetically, and Pharmacologically Intriguing Secondary Metabolites
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/b978-008044992-0.00308-4openalex-snapshot
Furans and their Benzo Derivatives: Applications
inferred← citeshttps://doi.org/10.1016/j.actatropica.2012.04.002openalex-snapshot
Activity of selected phytochemicals against Plasmodium falciparum
inferred← citeshttps://doi.org/10.1016/j.bse.2008.03.009openalex-snapshot
Flavaglines and triterpenes as chemical markers of Aglaia oligophylla
inferred← citeshttps://doi.org/10.1016/j.chembiol.2012.07.012openalex-snapshot
The Natural Anticancer Compounds Rocaglamides Inhibit the Raf-MEK-ERK Pathway by Targeting Prohibitin 1 and 2
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.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/s0031-9422(00)00205-3openalex-snapshot
Insecticidal rocaglamide derivatives from Aglaia spectabilis (Meliaceae)
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00761-xopenalex-snapshot
The absolute configuration of the mushroom metabolites involutin and chamonixin
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00014-5openalex-snapshot
A novel tandem reaction of 3-substituted coumarins with two equivalents of dimethylsulfoxonium ylide to 2-substituted cyclopenta[b]benzofuran-3-ol derivatives
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/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s0959-6380(03)80019-3openalex-snapshot
Chapter 7 Seven-membered rings
inferred← citeshttps://doi.org/10.1016/s1874-6004(08)80010-xopenalex-snapshot
Chapter 6 A biomimetic approach to the rocaglamides employing photogeneration of oxidopyryliums derived from 3-hydroxyflavones
inferred← citeshttps://doi.org/10.1021/ja044798oopenalex-snapshot
A Biomimetic Approach to the Rocaglamides Employing Photogeneration of Oxidopyryliums Derived from 3-Hydroxyflavones
inferred← citeshttps://doi.org/10.1021/jo040120fopenalex-snapshot
Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris
inferred← citeshttps://doi.org/10.1021/jo202366copenalex-snapshot
Total Synthesis of (±)-Rocaglamide via Oxidation-Initiated Nazarov Cyclization
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/np034057lopenalex-snapshot
Aglacins I−K, Three Highly Methoxylated Lignans from Aglaia cordata
inferred← citeshttps://doi.org/10.1021/np060428xopenalex-snapshot
Cytotoxic Flavaglines and Bisamides from Aglaia edulis
inferred← citeshttps://doi.org/10.1021/ol017304qopenalex-snapshot
Unprecedented Microwave Effects on the Cycloaddition of Fulvenes. A New Approach to the Construction of Polycyclic Ring Systems
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/10.11588/heidok.00013237openalex-snapshot
Molecular mechanisms of anti-proliferative effects of the Traditional Chinese Medicinal compound Rocaglamide A on cancers
inferred← citeshttps://doi.org/10.1201/9780203165584-20openalex-snapshot
Distribution, fate, and impact of pesticides in the tropical marine environment of Vietnam
inferred← citeshttps://doi.org/10.1201/9780203165584.ch8openalex-snapshot
Distribution, fate, and impact of pesticides in the tropical marine environment of Vietnam
inferred← citeshttps://doi.org/10.1248/cpb.54.1344openalex-snapshot
Potent Cytotoxic Rocaglamide Derivatives from the Fruits of Amoora cucullata
inferred← citeshttps://doi.org/10.12692/ijb/14.4.418-427openalex-snapshot
Cytotoxicity of bark extracts from Aglaia loheri (Blanco) Merr. (Meliaceae) against human colorectal carcinoma cells (HCT116)
inferred← citeshttps://doi.org/10.14348/molcells.2015.2353openalex-snapshot
Rocaglamide-A Potentiates Osteoblast Differentiation by Inhibiting NF-κB Signaling
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
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/10.5402/2011/239817openalex-snapshot
Progress in the Total Synthesis of Rocaglamide
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