Evidence map›Paper›PMID 29126729›Full record

ArticleEuropean journal of medicinal chemistry2018

Indole and Benzimidazole Bichalcophenes: Synthesis, DNA Binding and Antiparasitic Activity.

Abdelbasset A Farahat, Mohamed A Ismail, Arvind Kumar, Tanja Wenzler, Reto Brun, Ananya Paul, W David Wilson, David W Boykin

Open access · hybridAbstract read
In one paragraph

Article in European journal of medicinal chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Escaping ESKAPE resistance:Royal Society open science · 2023
    Article
  10. RSC advances · 2022
    Article
  11. Journal of molecular structure · 2022
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Microindoline 581, an Indole Derivative fromIranian journal of pharmaceutical research : IJPR · 2020
    Article
  20. 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 3 institutions in 3 countries.

Abdelbasset A FarahatDepartment of Chemistry, Georgia State University, Atlanta, GA, 30303, United States; Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura 35516, Egypt. Electronic address: afarahat@gsu.edu.
Mohamed A IsmailDepartment of Chemistry, Faculty of Science, Mansoura University, Mansoura 35516, Egypt.
Arvind KumarDepartment of Chemistry, Georgia State University, Atlanta, GA, 30303, United States.
Tanja WenzlerSwiss Tropical and Public Health Institute, 4002 Basel, Switzerland; University of Basel, 4003 Basel, Switzerland.
Reto BrunSwiss Tropical and Public Health Institute, 4002 Basel, Switzerland; University of Basel, 4003 Basel, Switzerland.
Ananya PaulDepartment of Chemistry, Georgia State University, Atlanta, GA, 30303, United States.
W David WilsonDepartment of Chemistry, Georgia State University, Atlanta, GA, 30303, United States.
David W BoykinDepartment of Chemistry, Georgia State University, Atlanta, GA, 30303, United States.
Georgia State University · USMansoura University · EGSwiss Tropical and Public Health Institute · CH

Funding

Molecular Design for Specific Recognition of Functional DNA SequencesR01GM111749 · NIGMS · GEORGIA STATE UNIVERSITY · PI WILSON, W DAVID · 2014 to 2021
$2.5M
NIGMS NIH HHS R01 GM111749
6 · The paper itself

Abstract

A novel series of indole and benzimidazole bichalcophene diamidine derivatives were prepared to study their antimicrobial activity against the tropical parasites causing African sleeping sickness and malaria. The dicyanoindoles needed to synthesize the target diamidines were obtained through Stille coupling reactions while the bis-cyanobenzimidazoles intermediates were made via condensation/cyclization reactions of different aldehydes with 4-cyano-1,2-diaminobenzene. Different amidine synthesis methodologies namely, lithium bis-trimethylsilylamide (LiN[Si(CH3)

Indexed as

AnimalsBenzimidazolesCell SurvivalDisease Models, AnimalIndolesMiceParasitic Sensitivity TestsPentamidineTrypanocidal AgentsTrypanosoma brucei rhodesienseTrypanosomiasis, AfricanbenzimidazoleBenzimidazolesindoleIndolesPentamidineTrypanocidal AgentsAfrican sleeping sicknessAntimalarialDiamidinesDNA minor groove bindersMalariaPinner reactionStille couplingTrypanocidal

Identifiers

PMID29126729
PMCPMC5744864
OpenAlexW2766534471

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.