Evidence map›Paper›PMID 26617963›Full record

ArticleACS medicinal chemistry letters2015

Silicon Incorporated Morpholine Antifungals: Design, Synthesis, and Biological Evaluation.

Gorakhnath R Jachak, Remya Ramesh, Duhita G Sant, Shweta U Jorwekar, Manjusha R Jadhav, Santosh G Tupe, Mukund V Deshpande, D Srinivasa Reddy

Abstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Synthesis of hydrazides of heterocyclic amines and their antimicrobial and spasmolytic activity.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
    Article
  8. Review
  9. Article
  10. Inhibition of Phytosterol Biosynthesis by Azasterols.Molecules (Basel, Switzerland) · 2020
    Article
  11. Article
  12. Metabolism and Biological Activities of 4-Methyl-Sterols.Molecules (Basel, Switzerland) · 2019
    Review
  13. Article
  14. Article
  15. 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 2 institutions in 1 country.

Gorakhnath R JachakDivision of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
Remya RameshDivision of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
Duhita G SantDivision of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
Shweta U JorwekarDivision of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
Manjusha R JadhavNational Research Centre for Grapes , Manjri, Solapur Road, Pune-412307, India.
Santosh G TupeDivision of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
Mukund V DeshpandeDivision of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
D Srinivasa ReddyDivision of Organic Chemistry and Biochemical Sciences Division, CSIR-National Chemical Laboratory , Dr. Homi Bhabha Road, Pune-411008, India.
National Chemical Laboratory · INNational Research Centre for Grapes · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Known morpholine class antifungals (fenpropimorph, fenpropidin, and amorolfine) were synthetically modified through silicon incorporation to have 15 sila-analogues. Twelve sila-analogues exhibited potent antifungal activity against different human fungal pathogens such as Candida albicans, Candida glabrata, Candida tropicalis, Cryptococcus neoformans, and Aspergillus niger. Sila-analogue 24 (fenpropimorph analogue) was the best in our hands, which showed superior fungicidal potential than fenpropidin, fenpropimorph, and amorolfine. The mode of action of sila-analogues was similar to morpholines, i.e., inhibition of sterol reductase and sterol isomerase enzymes of ergosterol synthesis pathway.

Indexed as

Antifungal drugsCandida albicansergosterol biosynthesismorpholinessila-analogues

Identifiers

PMID26617963
PMCPMC4645241
OpenAlexW2410067170

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.