Evidence map›Paper›PMID 27766903›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2017

Synthesis of new Schiff bases bearing 1,2,4-triazole, thiazolidine and chloroazetidine moieties and their pharmacological evaluation.

Nadia G Kandile, Mansoura I Mohamed, Hind M Ismaeel

Abstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Development of Metal Complexes for Treatment of Coronaviruses.International journal of molecular sciences · 2022
    Article
  5. Article
  6. Article
  7. Review
  8. 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

3 authors.

Nadia G Kandilea Department of Chemistry, Faculty of Women , Ain Shams University , Heliopolis , Cairo , Egypt.
Mansoura I Mohameda Department of Chemistry, Faculty of Women , Ain Shams University , Heliopolis , Cairo , Egypt.
Hind M Ismaeela Department of Chemistry, Faculty of Women , Ain Shams University , Heliopolis , Cairo , Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New compounds based on oxindole moiety were synthesized via the reaction of 5-substitued isatins 1a-e with different nucleophiles such as benzidine, 3,3'-dimethoxybenzidine 2a,b and 2,6-diaminopyridine 3 to afford three different classes of bis-Schiff bases 4a-e, 5a-e and 6a-e, respectively. The structures of the new compounds were elucidated on the basis of their FTIR,

Indexed as

AzetidinesSchiff BasesThiazolidinesTriazolesazetidineAzetidinesSchiff BasesThiazolidinesTriazolesAnticancer drugsminimal inhibitory concentrationoxindole moietypathagonic bacteriaSchiff bases

Identifiers

PMID27766903
PMCPMC6009854

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.