Evidence map›Paper›PMID 30018257›Full record

ReviewMolecules (Basel, Switzerland)2018

Synthesis and Biological Activity of Sterol 14α-Demethylase and Sterol C24-Methyltransferase Inhibitors.

David J Leaver

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Novel Metabolites ofJournal of fungi (Basel, Switzerland) · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Open biology · 2022
    Article
  11. Review
  12. Microbial Sterolomics as a Chemical Biology Tool.Molecules (Basel, Switzerland) · 2018
    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

1 author at 1 institution in 1 country.

David J LeaverDepartment of Biology, Geology and Physical Sciences, Sul Ross State University, Alpine, TX 79832, USA. david.leaver@sulross.edu.
Sul Ross State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sterol 14α-demethylase (SDM) is essential for sterol biosynthesis and is the primary molecular target for clinical and agricultural antifungals. SDM has been demonstrated to be a valid drug target for antiprotozoal therapies, and much research has been focused on using SDM inhibitors to treat neglected tropical diseases such as human African trypanosomiasis (HAT), Chagas disease, and leishmaniasis. Sterol C24-methyltransferase (24-SMT) introduces the C24-methyl group of ergosterol and is an enzyme found in pathogenic fungi and protozoa but is absent from animals. This difference in sterol metabolism has the potential to be exploited in the development of selective drugs that specifically target 24-SMT of invasive fungi or protozoa without adversely affecting the human or animal host. The synthesis and biological activity of SDM and 24-SMT inhibitors are reviewed herein.

Indexed as

14-alpha Demethylase InhibitorsFungal ProteinsMethyltransferasesMycosesProtozoan InfectionsProtozoan ProteinsSterol 14-DemethylaseAnimalsHumans14-alpha Demethylase Inhibitorsdelta 24-sterol methyltransferaseFungal ProteinsMethyltransferasesProtozoan ProteinsSterol 14-Demethylaseantifungalsantiparasitic drugsazolesChagas diseasehuman African trypanosomiasismechanism-based inactivatorssterol 14α-demethylasesterol biosynthesissterol C24-methyltransferasesynthesis

Identifiers

PMID30018257
PMCPMC6099924
OpenAlexW2884522400

What OpenQuestion holds

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LicenceCC BY
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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.