Evidence map›Paper›PMID 32318543›Full record

ArticleFrontiers in chemistry2020

Investigations on the Anticancer Potential of Benzothiazole-Based Metallacycles.

Stephan Mokesch, Klaudia Cseh, Heiko Geisler, Michaela Hejl, Matthias H M Klose, Alexander Roller, Samuel M Meier-Menches, Michael A Jakupec, Wolfgang Kandioller, Bernhard K Keppler

Open access · goldAbstract read
In one paragraph

Article in Frontiers in chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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

10 authors at 2 institutions in 1 country.

Stephan MokeschInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Klaudia CsehInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Heiko GeislerInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Michaela HejlInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Matthias H M KloseInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Alexander RollerInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Samuel M Meier-MenchesResearch Cluster Translational Cancer Therapy Research, University of Vienna, Vienna, Austria.
Michael A JakupecInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Wolfgang KandiollerInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
Bernhard K KepplerInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
University of Vienna · ATLudwig Boltzmann Cluster for Cardiovascular Research · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of 2-phenylbenzothiazole derivatives and their corresponding organometallic ruthenium(II) and osmium(II) complexes were synthesized, designed to exploit both, the attributes of the half-sandwich transition metal scaffold and the bioactivity spectrum of the applied 2-phenylbenzothiazoles. All synthesized compounds were characterized via standard analytical methods. The obtained organometallics showed antiproliferative activity in the low μM range and are thus at least an order of magnitude more potent than the free ligands. ESI-MS measurements showed that the examined compounds were stable in aqueous solution over 48 h. Additionally, their binding preferences to small biomolecules, their cellular accumulation and capacity of inducing apoptosis/necrosis were investigated. Based on the fluorescence properties of the selected ligand and the corresponding ruthenium complex, their subcellular distribution was studied by fluorescence microscopy, revealing a high degree of colocalization with acidic organelles of cancer cells.

Indexed as

anticancerbenzothiazolesmetallacyclesosmium complexesruthenium complexes

Identifiers

PMID32318543
PMCPMC7147246
OpenAlexW3014865614

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.