Evidence map›Paper›PMID 29415009›Full record

ArticlePloS one2018

Synthesis of magnolol and honokiol derivatives and their effect against hepatocarcinoma cells.

Margherita Maioli, Valentina Basoli, Paola Carta, Davide Fabbri, Maria Antonietta Dettori, Sara Cruciani, Pier Andrea Serra, Giovanna Delogu

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.3field-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

23 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  4. Proapoptotic and Antiproliferative Effects of the Desert TruffleEvidence-based complementary and alternative medicine : eCAM · 2023
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  5. Natural and natural-like polyphenol compounds:Archives of medical science : AMS · 2023
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  15. Article
  16. Review
  17. Molecules (Basel, Switzerland) · 2019
    Article
  18. Article
  19. Article
  20. 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

8 authors at 2 institutions in 2 countries.

Margherita MaioliDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Valentina BasoliDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Paola CartaInstitute of Biomolecular Chemistry, National Research Council, Sassari, Italy.
Davide FabbriInstitute of Biomolecular Chemistry, National Research Council, Sassari, Italy.
Maria Antonietta DettoriInstitute of Biomolecular Chemistry, National Research Council, Sassari, Italy.
Sara CrucianiDepartment of Biomedical Sciences, University of Sassari, Sassari, Italy.
Pier Andrea SerraCentre for Developmental Biology and Reprogramming (CEDEBIOR), Department of Biomedical Sciences, University of Sassari, Sassari, Italy.
Giovanna DeloguInstitute of Biomolecular Chemistry, National Research Council, Sassari, Italy.ORCID 0000-0001-8650-387X
National Research Council · ITUniversity of Sassari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hepatocellular carcinoma is one of the most common malignant tumour with high level of mortality rate due to its rapid progression and high resistance to conventional chemotherapies. Thus, the search for novel therapeutic leads is of global interest. Herein, a small set of derivatives of magnolol 1 and honokiol 2, the main components of Magnolia grandiflora and Magnolia obovata, were evaluated in in vitro assay using tumoral hepatocytes. The pro-drug approach was applied as versatile strategy to the improve bioactivity of the compounds by careful transformation of the hydroxyl groups of magnolol 1 and honokiol 2 in suitable ester derivatives. Compounds 10 and 11 resulted to be more potent than the parental honokiol 2 at concentration down to 1 μM with complete viability of treated fibroblast cells up to concentrations of 80 μM. The combination of a butyrate ester and a bare phenol-OH group in the honokiol structure seemed to play a significant role in the antiproliferative activity identifying an interesting pharmacological clue against hepatocellular carcinoma.

Indexed as

Allyl CompoundsBiphenyl CompoundsCarbon-13 Magnetic Resonance SpectroscopyCarcinoma, HepatocellularCell LineCell Line, TumorDrug Screening Assays, AntitumorHumansLignansLiver NeoplasmsPhenolsProton Magnetic Resonance SpectroscopyAllyl CompoundsBiphenyl CompoundshonokiolLignansmagnololPhenols

Identifiers

PMID29415009
PMCPMC5802897
OpenAlexW2793006597

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.