Evidence map›Paper›PMID 30126306›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2018

Design, synthesis, and evaluation of curcumin analogues as potential inhibitors of bacterial sialidase.

Bo Ram Kim, Ji-Young Park, Hyung Jae Jeong, Hyung-Jun Kwon, Su-Jin Park, In-Chul Lee, Young Bae Ryu, Woo Song Lee

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Sialidase Inhibitors with Different Mechanisms.Journal of medicinal chemistry · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Sialidases FromFrontiers in cellular and infection microbiology · 2019
    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

8 authors at 1 institution in 1 country.

Bo Ram Kima Bio-processing Technology Development and Support Team , Korea Research Institute of Bioscience and Biotechnology , Jeongeup , Republic of Korea.
Ji-Young Parkb Natural Product Material Research Center , Korea Research Institute of Bioscience and Biotechnology , Jeongeup , Republic of Korea.
Hyung Jae Jeonga Bio-processing Technology Development and Support Team , Korea Research Institute of Bioscience and Biotechnology , Jeongeup , Republic of Korea.
Hyung-Jun Kwonb Natural Product Material Research Center , Korea Research Institute of Bioscience and Biotechnology , Jeongeup , Republic of Korea.
Su-Jin Parkb Natural Product Material Research Center , Korea Research Institute of Bioscience and Biotechnology , Jeongeup , Republic of Korea.
In-Chul Leeb Natural Product Material Research Center , Korea Research Institute of Bioscience and Biotechnology , Jeongeup , Republic of Korea.
Young Bae Ryub Natural Product Material Research Center , Korea Research Institute of Bioscience and Biotechnology , Jeongeup , Republic of Korea.
Woo Song Leeb Natural Product Material Research Center , Korea Research Institute of Bioscience and Biotechnology , Jeongeup , Republic of Korea.
Korea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sialidases are key virulence factors that remove sialic acid from the host cell surface glycan, unmasking receptors that facilitate bacterial adherence and colonisation. In this study, we developed potential agents for treating bacterial infections caused by Streptococcus pneumoniae Nan A that inhibit bacterial sialidase using Turmeric and curcumin analogues. Design, synthesis, and structure analysis relationship (SAR) studies have been also described. Evaluation of the synthesised derivatives demonstrated that compound 5e was the most potent inhibitor of S. pneumoniae sialidase (IC

Indexed as

Drug DesignAnti-Bacterial AgentsCurcuminDose-Response Relationship, DrugEnzyme InhibitorsMicrobial Sensitivity TestsMolecular StructureNeuraminidaseStreptococcus pneumoniaeStructure-Activity RelationshipAnti-Bacterial AgentsCurcuminEnzyme InhibitorsNeuraminidaseCurcuminNan Asepsissialidase

Identifiers

PMID30126306
PMCPMC6104608
OpenAlexW2888134640

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.