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Chemistry and Biological Activity of Rocaglamide Derivatives and Related Compounds in Aglaia Species (Meliaceae)

https://doi.org/10.2174/1385272013375049

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inferredcites →https://doi.org/10.2307/1220495openalex-snapshot

Flora of Taiwan

inferredcites →https://doi.org/10.5962/bhl.title.10921openalex-snapshot

The flora of the Malay Peninsula

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Enantioselective Synthesis of the Complex Rocaglate (−)‐Silvestrol

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Stimulation of IRES‐Dependent Translation by Rocaglamide A Increases the Replication and Virulence of Cricket Paralysis Virus in Lepidopteran Insect Cells

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Comparative phytochemistry of flavaglines (= rocaglamides), a group of highly bioactive flavolignans from Aglaia species (Meliaceae)

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A Nucleotide Signature for Identification of Aglaia stellatopilosa Pannell

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Activity-guided isolation of cytotoxic constituents from the bark of Aglaia crassinervia collected in Indonesia

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Stereodivergent access to rocaglaol enabled by dual catalytic asymmetric allylation

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Stereodivergent total synthesis of rocaglaol initiated by synergistic dual-metal-catalyzed asymmetric allylation of benzofuran-3(2H)-one

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Molluscicidal activity of Aglaia duperreana and the constituents of its twigs and leaves

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inferred← citeshttps://doi.org/10.1016/j.phytol.2012.10.003openalex-snapshot

Two new rocaglamide derivatives from twigs of Aglaia odorata var. microphyllina

inferred← citeshttps://doi.org/10.1016/j.tet.2007.05.074openalex-snapshot

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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/10.1016/j.tet.2020.131257openalex-snapshot

Anti-inflammatory flavagline glycosides and putrescine bisamides from Aglaia perviridis leaves

inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.11.057openalex-snapshot

Biomimetic synthesis of the novel 1,4-dioxanyloxy fragment of silvestrol and episilvestrol

inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.09.062openalex-snapshot

Palladium catalysed arylation of 6,8-dimethoxybenzofuranone

inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.10.107openalex-snapshot

Edulisones A and B, two epimeric benzo[b]oxepine derivatives from the bark of Aglaia edulis

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/s1874-6004(08)80010-xopenalex-snapshot

Chapter 6 A biomimetic approach to the rocaglamides employing photogeneration of oxidopyryliums derived from 3-hydroxyflavones

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Cyclopenta[b]benzofuran and Secodammarane Derivatives from the Stems of Aglaia stellatopilosa

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Transition Metal-Catalyzed Direct Arylation of Substrates with Activated sp 3 -Hybridized C−H Bonds and Some of Their Synthetic Equivalents with Aryl Halides and Pseudohalides

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/ja062621jopenalex-snapshot

Enantioselective Photocycloaddition Mediated by Chiral Brønsted Acids: Asymmetric Synthesis of the Rocaglamides

inferred← citeshttps://doi.org/10.1021/ja300900popenalex-snapshot

Formal Synthesis of (±)-Methyl Rocaglate Using an Unprecedented Acetyl Bromide Mediated Nazarov Reaction

inferred← citeshttps://doi.org/10.1021/ja305342fopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/ja808402eopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/ja9029736openalex-snapshot

Nazarov Cyclization Initiated by Peracid Oxidation: The Total Synthesis of (±)-Rocaglamide

inferred← citeshttps://doi.org/10.1021/jacs.0c05113openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/jacs.9b06446openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/jm101318bopenalex-snapshot

Novel Flavaglines Displaying Improved Cytotoxicity

inferred← citeshttps://doi.org/10.1021/jm3011542openalex-snapshot

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inferred← citeshttps://doi.org/10.1021/jm900365vopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/jo040120fopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/jo100275qopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/jo202366copenalex-snapshot

Total Synthesis of (±)-Rocaglamide via Oxidation-Initiated Nazarov Cyclization

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

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inferred← citeshttps://doi.org/10.1021/np070184wopenalex-snapshot

Putrescine Bisamides from Aglaia gigantea

inferred← citeshttps://doi.org/10.1021/np200391copenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np300376fopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/np3007588openalex-snapshot

Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis

inferred← citeshttps://doi.org/10.1021/ol0479904openalex-snapshot

Stereoselective Synthesis of (±)-Rocaglaol Analogues

inferred← citeshttps://doi.org/10.1021/ol0513793openalex-snapshot

Stereospecific Synthesis of (±)-1,2-Anhydro Methyl Rocaglate

inferred← citeshttps://doi.org/10.1021/ol400401dopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/ol502615yopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/ol801435jopenalex-snapshot

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inferred← citeshttps://doi.org/10.1021/ol902067xopenalex-snapshot

Iodine(III)-Mediated Tandem Acetoxylation−Cyclization of o-Acyl Phenols for the Facile Construction of α-Acetoxy Benzofuranones

inferred← citeshttps://doi.org/10.1038/cdd.2010.99openalex-snapshot

Rocaglamide breaks TRAIL resistance in HTLV-1-associated adult T-cell leukemia/lymphoma by translational suppression of c-FLIP expression

inferred← citeshttps://doi.org/10.1038/s41573-022-00521-4openalex-snapshot

Targeting RNA structures with small molecules

inferred← citeshttps://doi.org/10.1038/s41598-018-37666-5openalex-snapshot

Oxo-aglaiastatin-Mediated Inhibition of Translation Initiation

inferred← citeshttps://doi.org/10.1038/srep20045openalex-snapshot

Cytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis

inferred← citeshttps://doi.org/10.1039/c1ob05109aopenalex-snapshot

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inferred← citeshttps://doi.org/10.1039/c4np00006dopenalex-snapshot

Rocaglamide, silvestrol and structurally related bioactive compounds from Aglaia species

inferred← citeshttps://doi.org/10.1039/c7sc03006aopenalex-snapshot

Enantioselective synthesis of cyclopenta[ b ]benzofurans via an organocatalytic intramolecular double cyclization

inferred← citeshttps://doi.org/10.1039/d2cc06324gopenalex-snapshot

Construction of cyclopenta[ b ]dihydronaphthofurans via TsOH-catalyzed consecutive biscyclization of dithioallylic alcohols and 1-styrylnaphthols

inferred← citeshttps://doi.org/10.1039/d2qo01916gopenalex-snapshot

Synthesis of cyclopenta[b]benzofurans via biomimetic oxidative phenol–enamine [3 + 2] cycloaddition

inferred← citeshttps://doi.org/10.1039/d6qo00085aopenalex-snapshot

Higher-order dearomative [10 + 2] cycloaddition of 2-nitrobenzofurans and 2-alkylidene-1-indanones to access pentacyclic scaffolds

inferred← citeshttps://doi.org/10.1079/pavsnnr20094049openalex-snapshot

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inferred← citeshttps://doi.org/10.1080/10286020.2012.730698openalex-snapshot

Triterpenoids fromAglaia odoratavar.microphyllina

inferred← citeshttps://doi.org/10.1080/10286020.2015.1057575openalex-snapshot

Two new lignans from twigs of Aglaia odorata

inferred← citeshttps://doi.org/10.1080/10286020.2015.1123694openalex-snapshot

Two new bisamides from the leaves of Aglaia perviridis

inferred← citeshttps://doi.org/10.1080/10286020801948367openalex-snapshot

Two new pregnanes fromAglaia perviridisHiern

inferred← citeshttps://doi.org/10.1080/14786419.2015.1016940openalex-snapshot

Cytotoxicity and Synergistic Effect of the Constituents from Roots ofAglaia odorata(Meliaceae)

inferred← citeshttps://doi.org/10.1124/mol.104.008177openalex-snapshot

A Synthetic Derivative of the Natural Product Rocaglaol Is a Potent Inhibitor of Cytokine-Mediated Signaling and Shows Neuroprotective Activity in Vitro and in Animal Models of Parkinson’s Disease and Traumatic Brain Injury

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/10.1177/1934578x1601101115openalex-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/10.1208/s12248-011-9273-xopenalex-snapshot

Characterization of Silvestrol Pharmacokinetics in Mice Using Liquid Chromatography–Tandem Mass Spectrometry

inferred← citeshttps://doi.org/10.1351/pac-con-08-10-16openalex-snapshot

Discovery of anticancer agents of diverse natural origin

inferred← citeshttps://doi.org/10.1371/journal.pone.0025302openalex-snapshot

Flavaglines Alleviate Doxorubicin Cardiotoxicity: Implication of Hsp27

inferred← citeshttps://doi.org/10.1515/znc-2013-3-402openalex-snapshot

Chemical Constituents from the Leaves of Aglaia odorata

inferred← citeshttps://doi.org/10.20902/ijctr.2019.120319openalex-snapshot

Biopesticide from Combination of Bitung (Barringtonia Asiatica L.Kurtz) Seed and Papaya (Carica Papaya) Sap

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/10.22146/ijc.25052openalex-snapshot

Cytotoxic Triterpenoids from the Stembark of Aglaia argentea (Meliaceae)

inferred← citeshttps://doi.org/10.23960/j.hptt.151-10openalex-snapshot

POLYTOMOUS QUANTAL RESPONSE OF CROCIDOLOMIA PAVONANA (F.) (LEPIDOPTERA: PYRALIDAE) TO EXTRACTS OF AGLAIA SPP. AND DYSOXYLUM SPP. (MELIACEAE)

inferred← citeshttps://doi.org/10.23960/j.hptt.211166-176openalex-snapshot

SINERGISME CENDAWAN ENTOMOPATOGEN Lecanicillium lecanii DENGAN INSEKTISIDA NABATI UNTUK MENINGKATKAN EFIKASI PENGENDALIAN TELUR KEPIK COKLAT Riptortus linearis PADA KEDELAI

inferred← citeshttps://doi.org/10.23960/j.hptt.2235-41openalex-snapshot

GANGGUAN BIOLOGI PADA CROCIDOLOMIA PAVONANA (F.) (LEPIDOPTERA: PYRALIDAE) AKIBAT PERLAKUAN DENGAN EKSTRAK BIJI AGLAIA ODORATISSIMA BLUME (MELIACEAE)

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/10.4049/jimmunol.174.11.7075openalex-snapshot

Rocaglamide Derivatives Are Immunosuppressive Phytochemicals That Target NF-AT Activity in T Cells

inferred← citeshttps://doi.org/10.4155/fmc.09.122openalex-snapshot

Inhibitors of Translation Initiation as Cancer Therapeutics

inferred← citeshttps://doi.org/10.4155/fmc.13.177openalex-snapshot

Flavaglines: Potent Anticancer Drugs that Target Prohibitins and the Helicase eIF4A

inferred← citeshttps://doi.org/10.5402/2011/239817openalex-snapshot

Progress in the Total Synthesis of Rocaglamide

inferred← citeshttps://doi.org/10.5560/znc.2013.68c0269openalex-snapshot

Cytotoxic Rocaglamide Derivatives from Aglaia duppereana

inferred← citeshttps://doi.org/10.57237/j.cse.2026.02.002openalex-snapshot

Research Advances in Dearomatization [3+2] Cycloaddi-tion/Cyclization Reactions of Heterocyclic Compounds

inferred← citeshttps://doi.org/10.70675/7d68b550za64ez450ez9652z105c70164939openalex-snapshot

Development of new approaches for the synthesis of flavaglines

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