Evidence map›Paper›PMID 26905758›Full record

ArticleThe Journal of antibiotics2016

Cladosporinone, a new viriditoxin derivative from the hypersaline lake derived fungus Cladosporium cladosporioides.

Yang Liu, Tibor Kurtán, Chang Yun Wang, Wen Han Lin, Raha Orfali, Werner Eg Müller, Georgios Daletos, Peter Proksch

Open access · bronzeAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in The Journal of antibiotics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Subcellular localization of fungal specialized metabolites.Fungal biology and biotechnology · 2022
    Review
  8. Review
  9. Article
  10. The GenusMolecules (Basel, Switzerland) · 2021
    Review
  11. 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 6 institutions in 4 countries.

Yang LiuInstitute of Pharmaceutical Biology and Biotechnology, Heinrich Heine University, Duesseldorf, Germany.
Tibor KurtánDepartment of Organic Chemistry, University of Debrecen, Debrecen, Hungary.
Chang Yun WangKey Laboratory of Marine Drugs, The Ministry of Education of China, School of Medicine and Pharmacy, Ocean University of China, Qingdao, People's Republic of China.
Wen Han LinState Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, People's Republic of China.
Raha OrfaliDepartment of Pharmacognosy, Faculty of Pharmacy, King Saud University, Riyadh, KSA.
Werner Eg MüllerInstitute of Physiological Chemistry, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Georgios DaletosInstitute of Pharmaceutical Biology and Biotechnology, Heinrich Heine University, Duesseldorf, Germany.
Peter ProkschInstitute of Pharmaceutical Biology and Biotechnology, Heinrich Heine University, Duesseldorf, Germany.
Heinrich Heine University Düsseldorf · DEKing Saud University · SAOcean University of China · CNPeking University · CNUniversity Medical Center of the Johannes Gutenberg University Mainz · DEUniversity of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A new cytotoxic viriditoxin derivative, cladosporinone (1), along with the known viriditoxin (2) and two viriditoxin derivatives (3 and 4) were obtained from the fungus Cladosporium cladosporioides isolated from the sediment of a hypersaline lake in Egypt. The structure of the new compound (1) was determined by 1D and 2D NMR measurements as well as by high-resolution ESIMS and electronic circular dichroism spectroscopy. All isolated compounds were studied for their cytotoxicity against the murine lymphoma cell line L5187Y and for their antibiotic activity against several pathogenic bacteria. Viriditoxin (2) was the most active compound in both bioassays. Compound 1 also exhibited strong cytotoxicity against the murine lymphoma cell line L5187Y with an IC50 value of 0.88 μm, whereas its antibiotic activity was weak.

Indexed as

AnimalsAnti-Bacterial AgentsAntineoplastic AgentsBacteriaCell Line, TumorCircular DichroismCladosporiumEgyptInhibitory Concentration 50LakesLymphomaMagnetic Resonance SpectroscopyMiceNaphtholsAnti-Bacterial AgentsAntineoplastic AgentsNaphtholsviriditoxin

Identifiers

PMID26905758
OpenAlexW2275149924

What OpenQuestion holds

Textmetadata
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.