Evidence map›Paper›PMID 31328585›Full record

ReviewJournal of enzyme inhibition and medicinal chemistry2019

Carbazole scaffolds in cancer therapy: a review from 2012 to 2018.

Samar Issa, Anthony Prandina, Nicolas Bedel, Pål Rongved, Saïd Yous, Marc Le Borgne, Zouhair Bouaziz

Abstract readReview
In one paragraph

Review in Journal of enzyme inhibition and medicinal chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
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

34 citing papers in PubMed.

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  13. Investigating the potential of monocyclic BJournal of molecular modeling · 2024
    Article
  14. Article
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  16. 5,8-Dimethyl-9Pharmaceuticals (Basel, Switzerland) · 2023
    Article
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  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

7 authors.

Samar Issaa Ecole de Biologie Industrielle, EBInnov , Cergy-Pontoise , France.ORCID http://orcid.org/0000-0003-2446-3512
Anthony Prandinab Faculté de Pharmacie - ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry, SFR Santé Lyon-Est CNRS UMS3453 - INSERM US7, Université de Lyon, Université Claude Bernard Lyon 1 , Lyon , France.ORCID http://orcid.org/0000-0002-7624-7654
Nicolas Bedelb Faculté de Pharmacie - ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry, SFR Santé Lyon-Est CNRS UMS3453 - INSERM US7, Université de Lyon, Université Claude Bernard Lyon 1 , Lyon , France.
Pål Rongvedc Department of Pharmaceutical Chemistry, School of Pharmacy, University of Oslo , Oslo , Norway.ORCID http://orcid.org/0000-0001-6678-1952
Saïd Yousd Université Lille, Inserm, CHU Lille, UMR-S 1172 JPArc Centre de Recherche Jean-Pierre Aubert Neurosciences et Cancer , Lille , France.ORCID http://orcid.org/0000-0001-9221-6535
Marc Le Borgneb Faculté de Pharmacie - ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry, SFR Santé Lyon-Est CNRS UMS3453 - INSERM US7, Université de Lyon, Université Claude Bernard Lyon 1 , Lyon , France.ORCID http://orcid.org/0000-0003-1398-075X
Zouhair Bouazizb Faculté de Pharmacie - ISPB, EA 4446 Bioactive Molecules and Medicinal Chemistry, SFR Santé Lyon-Est CNRS UMS3453 - INSERM US7, Université de Lyon, Université Claude Bernard Lyon 1 , Lyon , France.ORCID http://orcid.org/0000-0002-9948-0272

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For over half a century, the carbazole skeleton has been the key structural motif of many biologically active compounds including natural and synthetic products. Carbazoles have taken an important part in all the existing anti-cancer drugs because of their discovery from a large variety of organisms, including bacteria, fungi, plants, and animals. In this article, we specifically explored the literature from 2012 to 2018 on the anti-tumour activities reported to carbazole derivatives and we have critically collected the most significant data. The most described carbazole anti-tumour agents were classified according to their structure, starting from the tricyclic-carbazole motif to fused tetra-, penta-, hexa- and heptacyclic carbazoles. To date, three derivatives are available on the market and approved in cancer therapy.

Indexed as

AnimalsAntineoplastic AgentsCarbazolesCell ProliferationHumansMolecular StructureNeoplasmsAntineoplastic AgentsCarbazolescancerCarbazolecytotoxicityenzyme inhibitorstargeted therapy

Identifiers

PMID31328585
PMCPMC6691762

What OpenQuestion holds

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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.