Evidence map›Paper›PMID 32148676›Full record

ReviewIranian journal of microbiology2019

Unraveling the importance of molecules of natural origin in antifungal drug development through targeting ergosterol biosynthesis pathway.

Fatemehsadat Jamzivar, Masoomeh Shams-Ghahfarokhi, Mansoor Khoramizadeh, Niloufar Yousefi, Mohammadhassan Gholami-Shabani, Mehdi Razzaghi-Abyaneh

Open access · diamondAbstract readReview
In one paragraph

Review in Iranian journal of microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 24% 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, 13 citations in OpenAlex.

  1. Inhibition Mechanism ofFoods (Basel, Switzerland) · 2025
    Article
  2. Review
  3. Evaluation of Antifungal Selective Toxicity UsingJournal of fungi (Basel, Switzerland) · 2023
    Article
  4. Review
  5. Review
  6. 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

6 authors at 3 institutions in 1 country.

Fatemehsadat JamzivarDepartment of Mycology, Pasteur Institute of Iran, Tehran, Iran.
Masoomeh Shams-GhahfarokhiDepartment of Mycology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Mansoor KhoramizadehSchool of Iranian Traditional Medicine, Iran University of Medical Sciences, Tehran, Iran.
Niloufar YousefiDepartment of Mycology, Pasteur Institute of Iran, Tehran, Iran.
Mohammadhassan Gholami-ShabaniDepartment of Mycology, Pasteur Institute of Iran, Tehran, Iran.
Mehdi Razzaghi-AbyanehDepartment of Mycology, Pasteur Institute of Iran, Tehran, Iran.
Pasteur Institute of Iran · IRIran University of Medical Sciences · IRTarbiat Modares University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the past decades, the incidence of life-threatening fungal infections has increased dramatically in particular among patients with hampered immune function. Fungal infections cause around 1.5 million deaths annually, superior to malaria and tuberculosis. With respect to high toxicity, narrow spectrum of activity and drug resistance to current antifungals, there is an urgent need to discover novel leads from molecules of natural origin especially those derived from plants and microorganisms for antifungal drug discovery. Among antifungal drugs introduced into the clinic, those affecting ergosterol biosynthesis are still superior to other classes and the vital role of ergosterol in fungal growth and development. This review highlights current knowledge about available antifungal agents and further issues on antifungal drug discovery from compounds of natural origin which affect ergosterol biosynthesis. Special attention is made to the fungal sterol C24-methyltransferase (SMT), a crucial enzyme in ergosterol biosynthesis pathway as a novel target for rational drug design.

Indexed as

Antifungal drug discoveryErgosterol biosynthesisFungal infectionsNatural compounds

Identifiers

PMID32148676
PMCPMC7048963
OpenAlexW2999304316

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.