Evidence map›Paper›PMID 28891347›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2017

Synthesis and biological evaluation of aminomethyl and alkoxymethyl derivatives as carbonic anhydrase, acetylcholinesterase and butyrylcholinesterase inhibitors.

İlhami Gulçin, Malahat Abbasova, Parham Taslimi, Zübeyir Huyut, Leyla Safarova, Afsun Sujayev, Vagif Farzaliyev, Şükrü Beydemir, Saleh H Alwasel, Claudiu T Supuran

Open access · goldAbstract 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
12.0field-weighted citation impact, top 1% 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, 94 citations in OpenAlex.

  1. Drug Design of Carbonic Anhydrase Inhibitors.Sub-cellular biochemistry · 2026
    Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Isocoumarins: a new class of selective carbonic anhydrase IX and XII inhibitors.Journal of enzyme inhibition and medicinal chemistry · 2022
    Article
  8. Article
  9. Synthesis, characterisation, biological evaluation andJournal of enzyme inhibition and medicinal chemistry · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Isothiocyanates: cholinesterase inhibiting, antioxidant, and anti-inflammatory activity.Journal of enzyme inhibition and medicinal chemistry · 2018
    Article
  14. Article
  15. Article
  16. 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

10 authors at 6 institutions in 4 countries.

İlhami Gulçina Department of Chemistry, Faculty of Sciences , Ataturk University , Erzurum , Turkey.ORCID http://orcid.org/0000-0001-5993-1668
Malahat Abbasovac Laboratory of Theoretical Bases of Synthesis and Action Mechanism of Additives , Institute of Chemistry of Additives, Azerbaijan National Academy of Sciences , Baku , Azerbaijan.
Parham Taslimia Department of Chemistry, Faculty of Sciences , Ataturk University , Erzurum , Turkey.
Zübeyir Huyutd Department of Biochemistry, Faculty of Medical , Yüzüncü Yıl University , Van , Turkey.
Leyla Safarovac Laboratory of Theoretical Bases of Synthesis and Action Mechanism of Additives , Institute of Chemistry of Additives, Azerbaijan National Academy of Sciences , Baku , Azerbaijan.
Afsun Sujayevc Laboratory of Theoretical Bases of Synthesis and Action Mechanism of Additives , Institute of Chemistry of Additives, Azerbaijan National Academy of Sciences , Baku , Azerbaijan.
Vagif Farzaliyevc Laboratory of Theoretical Bases of Synthesis and Action Mechanism of Additives , Institute of Chemistry of Additives, Azerbaijan National Academy of Sciences , Baku , Azerbaijan.
Şükrü Beydemire Department of Biochemistry, Faculty of Pharmacy , Anadolu University , Eskişehir , Turkey.
Saleh H Alwaselb Department of Zoology, College of Science , King Saud University , Riyadh , Saudi Arabia.
Claudiu T Supuranf Dipartimento di Chimica Ugo Schiff , Universita degli Studi di Firenze , Florence , Italy.
Azerbaijan National Academy of Sciences · AZKing Saud University · SAAnadolu University · TRAtatürk University · TRUniversity of Florence · ITVan Yüzüncü Yıl Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Compounds containing nitrogen and sulfur atoms can be widely used in various fields such as industry, medicine, biotechnology and chemical technology. Therefore, the reactions of aminomethylation and alkoxymethylation of mercaptobenzothiazole, mercaptobenzoxazole and 2-aminothiazole were developed. Additionally, the alkoxymethyl derivatives of mercaptobenzoxazole and 2-aminothiazole were synthesized by a reaction with hemiformals, which are prepared by the reaction of alcohols and formaldehyde. In this study, the inhibitory effects of these molecules were investigated against acetylcholinesterase (AChE), butyrylcholinesterase (BChE) enzymes and carbonic anhydrase I, and II isoenzymes (hCA I and II). Both hCA isoenzymes were significantly inhibited by the recently synthesized molecules, with K

Indexed as

AcetylcholinesteraseBenzothiazolesBenzoxazolesButyrylcholinesteraseCarbonic Anhydrase InhibitorsCarbonic AnhydrasesCholinesterase InhibitorsDose-Response Relationship, DrugHumansMolecular StructureStructure-Activity RelationshipThiazoles2-aminothiazoleAcetylcholinesterasebenzothiazoleBenzothiazolesBenzoxazolesButyrylcholinesteraseCarbonic Anhydrase InhibitorsCarbonic AnhydrasesCholinesterase InhibitorsThiazolesAcetylcholinesterasebutyrylcholinesterasecarbonic anhydrasemercaptobenzothiazolemercaptobenzoxazole

Identifiers

PMID28891347
PMCPMC6445195
OpenAlexW2755562647

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.