Evidence map›Paper›PMID 23301897›Full record

ArticleJournal of natural products2013

Bioactive flavaglines and other constituents isolated from Aglaia perviridis.

Li Pan, Ulyana Muñoz Acuña, Jie Li, Nivedita Jena, Tran Ngoc Ninh, Caroline M Pannell, Heebyung Chai, James R Fuchs, Esperanza J Carcache de Blanco, Djaja D Soejarto and 1 more

Abstract read
In one paragraph

Article in Journal of natural products, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Article
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  8. Review
  9. Article
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  11. Review
  12. Dammarane-Type Triterpenoid from the Stem Bark ofMolecules (Basel, Switzerland) · 2022
    Article
  13. Article
  14. Two New Fatty Acid Derivatives, Omphalotols A and B and Anti-Pharmaceuticals (Basel, Switzerland) · 2022
    Article
  15. Comparative phytochemistry of flavaglines (= rocaglamides), a group of highly bioactive flavolignans fromPhytochemistry reviews : proceedings of the Phytochemical Society of Europe · 2022
    Review
  16. Antioxidant Phenylpropanoid Glycosides fromPlants (Basel, Switzerland) · 2021
    Article
  17. Review
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Li PanDivision of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, Ohio 43210, USA.
Ulyana Muñoz Acuña
Jie Li
Nivedita Jena
Tran Ngoc Ninh
Caroline M Pannell
Heebyung Chai
James R Fuchs
Esperanza J Carcache de Blanco
Djaja D Soejarto
A Douglas Kinghorn
The Ohio State University · USUniversity of Illinois Chicago · USVietnam Academy of Science and Technology · VN

Funding

Project 3:Isolation Chemistry of Filamentous Fungi and Biological EvaluationP01CA125066 · NCI · OHIO STATE UNIVERSITY · PI JAMES R FUCHS · 2007 to 2026
$27.2M
NCI NIH HHS P01 CA125066
6 · The paper itself

Abstract

Eight new compounds, including two cyclopenta[b]benzopyran derivatives (1, 2), two cyclopenta[b]benzofuran derivatives (3, 4), three cycloartane triterpenoids (5-7), and an apocarotenoid (8), together with 16 known compounds, were isolated from the chloroform-soluble partitions of separate methanol extracts of a combination of the fruits, leaves, and twigs and of the roots of Aglaia perviridis collected in Vietnam. Isolation work was monitored using human colon cancer cells (HT-29) and facilitated with an LC/MS dereplication procedure. The structures of the new compounds (1-8) were determined on the basis of spectroscopic data interpretation. The Mosher ester method was employed to determine the absolute configurations of 5-7, and the absolute configuration of the 9,10-diol unit of compound 8 was established by a dimolybdenum tetraacetate [Mo2(AcO)4] induced circular dichroism procedure. Seven known rocaglate derivatives (9-15) exhibited significant cytotoxicity against the HT-29 cell line, with rocaglaol (9) being the most potent (ED50 0.0007 μM). The new compounds 2-4 were also active against this cell line, with ED50 values ranging from 0.46 to 4.7 μM. The cytotoxic compounds were evaluated against a normal colon cell line, CCD-112CoN. In addition, the new compound perviridicin B (2), three known rocaglate derivatives (9, 11, 12), and a known sesquiterpene, 2-oxaisodauc-5-en-12-al (17), showed significant NF-κB (p65) inhibitory activity in an ELISA assay.

Indexed as

AglaiaAntineoplastic Agents, PhytogenicBenzofuransBenzopyransDrug Screening Assays, AntitumorHT29 CellsHumansMolecular StructureNF-kappa BNuclear Magnetic Resonance, BiomolecularTriterpenesVietnamAntineoplastic Agents, PhytogenicBenzofuransBenzopyransNF-kappa BrocaglaolTriterpenes

Identifiers

PMID23301897
PMCPMC3606667
OpenAlexW2057521991

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.