Evidence map›Paper›PMID 32046220›Full record

ArticleMolecules (Basel, Switzerland)2020

Synthesis of Bisphenol Neolignans Inspired by Honokiol as Antiproliferative Agents.

Nunzio Cardullo, Vincenza Barresi, Vera Muccilli, Giorgia Spampinato, Morgana D'Amico, Daniele Filippo Condorelli, Corrado Tringali

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.8field-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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Neuroprotective Potency of Neolignans inFrontiers in pharmacology · 2022
    Pooled it
  2. Article
  3. Article
  4. Article
  5. The Potential ofMolecules (Basel, Switzerland) · 2023
    Review
  6. Article
  7. A Rare Natural Benzo[International journal of molecular sciences · 2020
    Article
  8. Rapha MyrInternational journal of molecular sciences · 2020
    Article
  9. 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

7 authors at 1 institution in 1 country.

Nunzio CardulloDepartment of Chemical Sciences, University of Catania, Viale A. Doria 6, 95125 Catania, Italy.
Vincenza BarresiDepartment of Biomedical and Biotechnological Sciences, Section of Medical Biochemistry, University of Catania, Via Santa Sofia 97, 95123 Catania, Italy.
Vera MuccilliDepartment of Chemical Sciences, University of Catania, Viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0002-6212-5154
Giorgia SpampinatoDepartment of Biomedical and Biotechnological Sciences, Section of Medical Biochemistry, University of Catania, Via Santa Sofia 97, 95123 Catania, Italy.
Morgana D'AmicoDepartment of Biomedical and Biotechnological Sciences, Section of Medical Biochemistry, University of Catania, Via Santa Sofia 97, 95123 Catania, Italy.
Daniele Filippo CondorelliDepartment of Biomedical and Biotechnological Sciences, Section of Medical Biochemistry, University of Catania, Via Santa Sofia 97, 95123 Catania, Italy.ORCID 0000-0002-0311-5386
Corrado TringaliDepartment of Chemical Sciences, University of Catania, Viale A. Doria 6, 95125 Catania, Italy.ORCID 0000-0003-4268-0115
University of Catania · IT

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca PRIN 2017 Project No. 2017A95NCJ_003Piano della ricerca di Ateneo, Intervento 2, University of Catania Years 2016-2018Università di Catania FIR 2014 - project No. 668A01
6 · The paper itself

Abstract

Honokiol (2) is a natural bisphenol neolignan showing a variety of biological properties, including antitumor activity. Some studies pointed out 2 as a potential anticancer agent in view of its antiproliferative and pro-apoptotic activity towards tumor cells. As a further contribution to these studies, we report here the synthesis of a small library of bisphenol neolignans inspired by honokiol and the evaluation of their antiproliferative activity. The natural lead was hence subjected to simple chemical modifications to obtain the derivatives 3-9; further neolignans (12a-c, 13a-c, 14a-c, and 15a) were synthesized employing the Suzuki-Miyaura reaction, thus obtaining bisphenols with a substitution pattern different from honokiol. These compounds and the natural lead were subjected to antiproliferative assay towards HCT-116, HT-29, and PC3 tumor cell lines. Six of the neolignans show GI

Indexed as

Allyl CompoundsAntineoplastic AgentsApoptosisBenzhydryl CompoundsBiphenyl CompoundsBisphenol A CompoundsCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorHCT116 CellsHT29 CellsHumansLignansPC-3 CellsPhenolsAllyl CompoundsAntineoplastic AgentsBenzhydryl CompoundsBiphenyl Compoundsbisphenol ABisphenol A CompoundshonokiolLignansPhenolsantitumor activityapoptosisbisphenol neolignanshonokiolpolyphenolsSuzuki–Miyaura cross-coupling

Identifiers

PMID32046220
PMCPMC7037512
OpenAlexW3005264044

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.