Evidence map›Paper›PMID 33608591›Full record

ArticleScientific reports2021

Synthesis of novel phytol-derived γ-butyrolactones and evaluation of their biological activity.

Anna Gliszczyńska, Katarzyna Dancewicz, Beata Gabryś, Marta Świtalska, Joanna Wietrzyk, Gabriela Maciejewska

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Anatomical and Metabolome Features ofInternational journal of molecular sciences · 2024
    Article
  6. Article
  7. Phytochemical Screening and Evaluation of Pesticidal Efficacy in the Oleoresins ofEvidence-based complementary and alternative medicine : eCAM · 2023
    Article
  8. Article
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

6 authors at 4 institutions in 1 country.

Anna GliszczyńskaDepartment of Chemistry, Wroclaw University of Environmental and Life Sciences, Norwida 25, 50-375, Wrocław, Poland. anna.gliszczynska@wp.pl.
Katarzyna DancewiczDepartment of Botany and Ecology, University of Zielona Góra, Szafrana 1, 65-516, Zielona Góra, Poland.
Beata GabryśDepartment of Botany and Ecology, University of Zielona Góra, Szafrana 1, 65-516, Zielona Góra, Poland.
Marta ŚwitalskaDepartment of Experimental Oncology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Science, Weigla 12, 53-114, Wrocław, Poland.
Joanna WietrzykDepartment of Experimental Oncology, Ludwik Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Science, Weigla 12, 53-114, Wrocław, Poland.
Gabriela MaciejewskaCentral Laboratory of Instrumental Analysis, Wrocław University of Science and Technology, Wybrzeże Wyspiańskiego 27, 50-370, Wrocław, Poland.
Ludwik Hirszfeld Institute of Immunology and Experimental Therapy · PLUniversity of Zielona Góra · PLAGH University of Krakow · PLWroclaw University of Environmental and Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis of phytol-derived γ-butyrolactones as well as their evaluation for deterrent activity towards peach-potato aphid Myzus persicae and antiproliferative activity against four selected cancer cell lines are reported. Products were obtained in good yields (19-96%) and their structures were fully characterized by spectroscopic data (NMR, HRMS). Four synthesized δ-halo-γ-lactones (4-7) are new and have not been previously described in the literature. In the choice test phytol (1) appeared deterrent to M. persicae, whereas modifications of its structure did not cause the avoidance of the treated leaves by the aphids. In contrast, aphids were attracted to the leaves treated with the new trans-δ-chloro-γ-lactone (6). Electrical Penetration Graph (EPG) technique applied to explore the aphid probing and feeding activity revealed that neither phytol nor lactone 6 affected aphid probing and the consumption of phloem sap, which means that both phytol and the lactone 6 might have acted as postingestive modifiers of aphid behavior. The results of in vitro antitumor assays showed that obtained phytol derivatives exhibit cytotoxic activity against studied cancer cell lines (leukemia, lung and colon carcinoma and its doxorubicin resistant subline). Halolactones 4-6 were identified as the compounds, which arrest cell cycle of leukemia cells mainly in G2/M and S phases.

Indexed as

4-ButyrolactoneAnimalsAntineoplastic AgentsCaspase 3Caspase 7Cell CycleCell LineCell ProliferationChemistry Techniques, SyntheticChromatography, Thin LayerGas Chromatography-Mass SpectrometryGene Expression RegulationHumansMicePhytolStructure-Activity Relationship4-ButyrolactoneAntineoplastic AgentsCaspase 3Caspase 7Phytol

Identifiers

PMID33608591
PMCPMC7896091
OpenAlexW3131085111

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.