Evidence map›Paper›PMID 36793764›Full record

ArticleFrontiers in chemistry2023

Half sandwich-type osmium, ruthenium, iridium and rhodium complexes with bidentate glycosyl heterocyclic ligands induce cytostasis in platinum-resistant ovarian cancer cells and bacteriostasis in Gram-positive multiresistant bacteria.

István Kacsir, Adrienn Sipos, Tímea Kiss, Evelin Major, Nikolett Bajusz, Emese Tóth, Péter Buglyó, László Somsák, Gábor Kardos, Péter Bai and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Recent Advances in Anticancer Research of Osmium and Rhodium Complexes.Medicinal chemistry (Shariqah (United Arab Emirates)) · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Half-Sandwich Type Platinum-Group Metal Complexes ofMolecules (Basel, Switzerland) · 2023
    Article
  10. 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

11 authors at 2 institutions in 1 country.

István KacsirDepartment of Organic Chemistry, University of Debrecen, Debrecen, Hungary.
Adrienn SiposDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Tímea KissDepartment of Organic Chemistry, University of Debrecen, Debrecen, Hungary.
Evelin MajorDepartment of Metagenomics, University of Debrecen, Debrecen, Hungary.
Nikolett BajuszDepartment of Metagenomics, University of Debrecen, Debrecen, Hungary.
Emese TóthDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Péter BuglyóDepartment of Inorganic and Analytical Chemistry, Faculty of Sciences and Technology, University of Debrecen, Debrecen, Hungary.
László SomsákDepartment of Organic Chemistry, University of Debrecen, Debrecen, Hungary.
Gábor KardosDepartment of Metagenomics, University of Debrecen, Debrecen, Hungary.
Péter BaiDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Éva BokorDepartment of Organic Chemistry, University of Debrecen, Debrecen, Hungary.
University of Debrecen · HUNational Research, Development and Innovation Office · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The toxicity of and resistance to platinum complexes as cisplatin, oxaliplatin or carboplatin calls for the replacement of these therapeutic agents in clinical settings. We have previously identified a set of half sandwich-type osmium, ruthenium and iridium complexes with bidentate glycosyl heterocyclic ligands exerting specific cytostatic activity on cancer cells but not on non-transformed primary cells. The apolar nature of the complexes, conferred by large, apolar benzoyl protective groups on the hydroxyl groups of the carbohydrate moiety, was the main molecular feature to induce cytostasis. We exchanged the benzoyl protective groups to straight chain alkanoyl groups with varying length (3 to 7 carbon units) that increased the IC

Indexed as

glycosyl triazolehalf-sandwich complexMRSAovarian cancerquinolinereactive oxygen species productionsarcomaVRE

Identifiers

PMID36793764
PMCPMC9923724
OpenAlexW4318478080

What Socratic 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 Socratic graph.