Evidence map›Paper›PMID 33920838›Full record

ArticlePharmaceuticals (Basel, Switzerland)2021

Dual-Target Compounds against Type 2

Ádám Sipos, Eszter Szennyes, Nikolett Éva Hajnal, Sándor Kun, Katalin E Szabó, Karen Uray, László Somsák, Tibor Docsa, Éva Bokor

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2021. 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
1.8field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Synthesis, In Silico and Kinetics Evaluation ofInternational journal of molecular sciences · 2024
    Article
  5. Article
  6. Synthesis, X-ray diffraction analysis, quantum chemical studies andJournal of enzyme inhibition and medicinal chemistry · 2022
    Article
  7. Article
  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

9 authors at 1 institution in 1 country.

Ádám SiposDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Eszter SzennyesDepartment of Organic Chemistry, University of Debrecen, POB 400, H-4002 Debrecen, Hungary.
Nikolett Éva HajnalDepartment of Organic Chemistry, University of Debrecen, POB 400, H-4002 Debrecen, Hungary.
Sándor KunDepartment of Organic Chemistry, University of Debrecen, POB 400, H-4002 Debrecen, Hungary.
Katalin E SzabóDepartment of Organic Chemistry, University of Debrecen, POB 400, H-4002 Debrecen, Hungary.
Karen UrayDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.ORCID 0000-0001-6997-459X
László SomsákDepartment of Organic Chemistry, University of Debrecen, POB 400, H-4002 Debrecen, Hungary.ORCID 0000-0002-9103-9845
Tibor DocsaDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Egyetem tér 1, H-4032 Debrecen, Hungary.
Éva BokorDepartment of Organic Chemistry, University of Debrecen, POB 400, H-4002 Debrecen, Hungary.
University of Debrecen · HU

Funding

European Regional Development Fund GINOP-2.3.2-15-2016-00008, GINOP-2.3.3-15-2016-00004Nemzeti Kutatási Fejlesztési és Innovációs Hivatal FK125067, FK132222
6 · The paper itself

Abstract

A current trend in the quest for new therapies for complex, multifactorial diseases, such as diabetes mellitus (DM), is to find dual or even multi-target inhibitors. In DM, the sodium dependent glucose cotransporter 2 (SGLT2) in the kidneys and the glycogen phosphorylase (GP) in the liver are validated targets. Several (β-D-glucopyranosylaryl)methyl (het)arene type compounds, called gliflozins, are marketed drugs that target SGLT2. For GP, low nanomolar glucose analogue inhibitors exist. The purpose of this study was to identify dual acting compounds which inhibit both SGLTs and GP. To this end, we have extended the structure-activity relationships of SGLT2 and GP inhibitors to scarcely known (

Indexed as

1,2,3- and 1,2,4-triazole1,2,4- and 1,3,4-oxadiazoleC-glucosyl heterocycledual-target inhibitorglycogen phosphorylaseimidazolepyrimidinesodium dependent glucose cotransporterthiazole

Identifiers

PMID33920838
PMCPMC8071193
OpenAlexW3153618077

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.