On the public citation graph

Structurally Modified Cyclopenta[b]benzofuran Analogues Isolated from Aglaia perviridis

https://doi.org/10.1021/acs.jnatprod.9b00631

0 signed · 79 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.

Claim with ORCID

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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1096-987x(199604)17:5/6<520::aid-jcc2>3.0.co;2-wopenalex-snapshot

Merck molecular force field. II. MMFF94 van der Waals and electrostatic parameters for intermolecular interactions

inferredcites →https://doi.org/10.1002/(sici)1096-987x(199604)17:5/6<587::aid-jcc4>3.0.co;2-qopenalex-snapshot

Merck molecular force field. IV. conformational energies and geometries for MMFF94

inferredcites →https://doi.org/10.1002/(sici)1096-987x(199604)17:5/6<616::aid-jcc5>3.0.co;2-xopenalex-snapshot

Merck molecular force field. V. Extension of MMFF94 using experimental data, additional computational data, and empirical rules

inferredcites →https://doi.org/10.1002/(sici)1096-987x(199604)17:6<490::aid-jcc1>3.3.co;2-vopenalex-snapshot

inferredcites →https://doi.org/10.1002/(sici)1096-987x(199604)17:6<553::aid-jcc3>3.3.co;2-hopenalex-snapshot

inferredcites →https://doi.org/10.1002/9783527684403.ch7openalex-snapshot

Bioactive Flavaglines: Synthesis and Pharmacology

inferredcites →https://doi.org/10.1002/anie.200702700openalex-snapshot

Total Synthesis of (−)‐Episilvestrol and (−)‐Silvestrol

inferredcites →https://doi.org/10.1002/anie.200702707openalex-snapshot

Enantioselective Synthesis of the Complex Rocaglate (−)‐Silvestrol

inferredcites →https://doi.org/10.1002/chir.22600openalex-snapshot

Good Computational Practice in the Assignment of Absolute Configurations by TDDFT Calculations of ECD Spectra

inferredcites →https://doi.org/10.1002/jcc.1058openalex-snapshot

6‐31G* basis set for third‐row atoms

inferredcites →https://doi.org/10.1002/jcc.540111013openalex-snapshot

Compact contracted basis sets for third‐row atoms: Ga–Kr

inferredcites →https://doi.org/10.1007/978-3-319-93506-5_1openalex-snapshot

The Search for Anticancer Agents from Tropical Plants

inferredcites →https://doi.org/10.1007/978-3-7091-0748-5_1openalex-snapshot

Chemistry and Biology of Rocaglamides (= Flavaglines) and Related Derivatives from Aglaia Species (Meliaceae)

inferredcites →https://doi.org/10.1007/bf00533485openalex-snapshot

The influence of polarization functions on molecular orbital hydrogenation energies

inferredcites →https://doi.org/10.1007/s00214-007-0310-xopenalex-snapshot

The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals

inferredcites →https://doi.org/10.1007/s10600-016-1665-9openalex-snapshot

A New Triterpeniod from Aglaia perviridis

inferredcites →https://doi.org/10.1016/0009-2614(80)80628-2openalex-snapshot

The isomers of silacyclopropane

inferredcites →https://doi.org/10.1016/0031-9422(92)80108-qopenalex-snapshot

Rocaglamide, a natural benzofuran insecticide from Aglaia odorata

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.antiviral.2018.07.010openalex-snapshot

The natural compound silvestrol inhibits hepatitis E virus (HEV) replication in vitro and in vivo

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.chembiol.2012.07.012openalex-snapshot

The Natural Anticancer Compounds Rocaglamides Inhibit the Raf-MEK-ERK Pathway by Targeting Prohibitin 1 and 2

inferredcites →https://doi.org/10.1016/j.cplett.2004.06.011openalex-snapshot

A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP)

inferredcites →https://doi.org/10.1016/j.jorganchem.2004.06.028openalex-snapshot

Palladium-catalyzed heteroannulation of cyclic alkenes by functionally substituted aryl iodides

inferredcites →https://doi.org/10.1016/j.molcel.2018.11.026openalex-snapshot

The Translation Inhibitor Rocaglamide Targets a Bimolecular Cavity between eIF4A and Polypurine RNA

inferredcites →https://doi.org/10.1021/acs.jnatprod.5b00810openalex-snapshot

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

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00924openalex-snapshot

Cardiac Glycoside Constituents of Streblus asper with Potential Antineoplastic Activity

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/jm101318bopenalex-snapshot

Novel Flavaglines Displaying Improved Cytotoxicity

inferredcites →https://doi.org/10.1021/jm3011542openalex-snapshot

Synthetic Silvestrol Analogues as Potent and Selective Protein Synthesis Inhibitors

inferredcites →https://doi.org/10.1021/jm301201zopenalex-snapshot

Flavaglines as Potent Anticancer and Cytoprotective Agents

inferredcites →https://doi.org/10.1021/jm900365vopenalex-snapshot

Synthetic Analogue of Rocaglaol Displays a Potent and Selective Cytotoxicity in Cancer Cells: Involvement of Apoptosis Inducing Factor and Caspase-12

inferredcites →https://doi.org/10.1021/jo040008hopenalex-snapshot

Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris.

inferredcites →https://doi.org/10.1021/jo040120fopenalex-snapshot

Silvestrol and Episilvestrol, Potential Anticancer Rocaglate Derivatives from Aglaia silvestris

inferredcites →https://doi.org/10.1021/np100503qopenalex-snapshot

Isolation and Characterization of Minor Analogues of Silvestrol and Other Constituents from a Large-Scale Re-collection of Aglaia foveolata

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/np3007588openalex-snapshot

Bioactive Flavaglines and Other Constituents Isolated from Aglaia perviridis

inferredcites →https://doi.org/10.1021/ol400401dopenalex-snapshot

Synthesis of Biotinylated Episilvestrol: Highly Selective Targeting of the Translation Factors eIF4AI/II

inferredcites →https://doi.org/10.1038/srep20045openalex-snapshot

Cytotoxic Rocaglate Derivatives from Leaves of Aglaia perviridis

inferredcites →https://doi.org/10.1039/b508541aopenalex-snapshot

Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy

inferredcites →https://doi.org/10.1039/b515623hopenalex-snapshot

Accurate Coulomb-fitting basis sets for H to Rn

inferredcites →https://doi.org/10.1039/b810189bopenalex-snapshot

Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections

inferredcites →https://doi.org/10.1039/c39820001150openalex-snapshot

X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifolia

inferredcites →https://doi.org/10.1039/c4np00006dopenalex-snapshot

Rocaglamide, silvestrol and structurally related bioactive compounds from Aglaia species

inferredcites →https://doi.org/10.1063/1.1674657openalex-snapshot

Self-Consistent Molecular Orbital Methods. XI. Molecular Orbital Theory of NMR Chemical Shifts

inferredcites →https://doi.org/10.1063/1.1674902openalex-snapshot

Self-Consistent Molecular-Orbital Methods. IX. An Extended Gaussian-Type Basis for Molecular-Orbital Studies of Organic Molecules

inferredcites →https://doi.org/10.1063/1.444267openalex-snapshot

Self-consistent molecular orbital methods. XXIII. A polarization-type basis set for second-row elements

inferredcites →https://doi.org/10.1063/1.474865openalex-snapshot

Extension of Gaussian-2 (G2) theory to molecules containing third-row atoms K and Ca

inferredcites →https://doi.org/10.1063/1.476673openalex-snapshot

6-31G* basis set for atoms K through Zn

inferredcites →https://doi.org/10.1073/pnas.1713000115openalex-snapshot

Rocaglates as dual-targeting agents for experimental cerebral malaria

inferredcites →https://doi.org/10.1080/00268977400100171openalex-snapshot

Accuracy of AH n equilibrium geometries by single determinant molecular orbital theory

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/10.1182/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/10.1186/1756-8722-6-21openalex-snapshot

Silvestrol exhibits significant in vivo and in vitro antileukemic activities and inhibits FLT3 and miR-155 expressions in acute myeloid leukemia

inferredcites →https://doi.org/10.1186/1758-2946-3-33openalex-snapshot

Open Babel: An open chemical toolbox

inferredcites →https://doi.org/10.1186/s12885-015-1988-0openalex-snapshot

Silvestrol induces early autophagy and apoptosis in human melanoma cells

inferredcites →https://doi.org/10.1208/s12248-011-9276-7openalex-snapshot

Resistance to the Translation Initiation Inhibitor Silvestrol is Mediated by ABCB1/P-Glycoprotein Overexpression in Acute Lymphoblastic Leukemia Cells

inferredcites →https://doi.org/10.1248/cpb.54.1344openalex-snapshot

Potent Cytotoxic Rocaglamide Derivatives from the Fruits of Amoora cucullata

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/10.21873/anticanres.11146openalex-snapshot

Discovery of Anticancer Agents of Diverse Natural Origin

inferredcites →https://doi.org/10.5012/bkcs.2010.31.9.2665openalex-snapshot

Bisamides from the Twigs of Aglaia perviridis Collected in Vietnam

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.2022.113301zenodo-depositor-declared

Anti-inflammatory withanolides from the aerial parts of Physalis minima

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/vjch.202400102openalex-snapshot

The genus Aglaia: Diversity in chemical structure 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/j.aquaculture.2023.739710openalex-snapshot

Study on the inhibitory effect of rocaglamide against Micropterus salmoides rhabdovirus (MSRV)

inferred← citeshttps://doi.org/10.1016/j.bmc.2019.115301openalex-snapshot

Cytotoxic and non-cytotoxic cardiac glycosides isolated from the combined flowers, leaves, and twigs of Streblus asper

inferred← citeshttps://doi.org/10.1016/j.jep.2025.120474openalex-snapshot

The continuing need for taxonomic input in phytochemical research

inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114439openalex-snapshot

Structurally diverse dammarane-derived triterpenoids from the twigs of Aglaia perviridis Hiern and their α-glucosidase and PTP1B inhibitory activities

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.3c00948openalex-snapshot

Design and Synthesis of Cytotoxic Water-Soluble Rocaglaol Derivatives against HEL Cells by Inhibiting Fli-1

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/10.1039/c9ra09542jopenalex-snapshot

Stewartiacids A–N, C-23 carboxylated triterpenoids from Chinese Stewartia and their inhibitory effects against ATP-citrate lyase and NF-κB

inferred← citeshttps://doi.org/10.1039/d2np00080fopenalex-snapshot

Strategies for the discovery of potential anticancer agents from plants collected from Southeast Asian tropical rainforests as a case study

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/10.1055/a-1401-9562openalex-snapshot

Update on Phytochemical and Biological Studies on Rocaglate Derivatives from Aglaia Species

inferred← citeshttps://doi.org/10.1186/s43094-024-00682-6openalex-snapshot

Identification and characterization of phytochemicals in methanolic extract of roots of Datura fastuosa using various techniques

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.