Evidence map›Paper›PMID 35425287›Full record

ArticleRSC advances2022

Integrated

Dina S Ghallab, Eman Shawky, Ali M Metwally, Ismail Celik, Reham S Ibrahim, Mohamed M Mohyeldin

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 42 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Dina S GhallabDepartment of Pharmacognosy, Faculty of Pharmacy, Alexandria University Alexandria 21521 Egypt rehamsaid84@yahoo.com reham.abdelkader@alexu.edu.eg +20-1223821098.
Eman ShawkyDepartment of Pharmacognosy, Faculty of Pharmacy, Alexandria University Alexandria 21521 Egypt rehamsaid84@yahoo.com reham.abdelkader@alexu.edu.eg +20-1223821098.ORCID https://orcid.org/0000-0003-0089-9629
Ali M MetwallyDepartment of Pharmacognosy, Faculty of Pharmacy, Alexandria University Alexandria 21521 Egypt rehamsaid84@yahoo.com reham.abdelkader@alexu.edu.eg +20-1223821098.
Ismail CelikDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Erciyes University Kayseri 38039 Turkey.
Reham S IbrahimDepartment of Pharmacognosy, Faculty of Pharmacy, Alexandria University Alexandria 21521 Egypt rehamsaid84@yahoo.com reham.abdelkader@alexu.edu.eg +20-1223821098.ORCID https://orcid.org/0000-0002-8208-5014
Mohamed M MohyeldinDepartment of Pharmacognosy, Faculty of Pharmacy, Alexandria University Alexandria 21521 Egypt rehamsaid84@yahoo.com reham.abdelkader@alexu.edu.eg +20-1223821098.
Alexandria University · EGErciyes University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Xanthine oxidase (XO) has been well-recognized as a validated target for the treatment of hyperuricemia and gout. Currently, there are two drugs in clinical use that shut down XO overactivity, allopurinol and febuxostat; however, detrimental side effects restrict their applications. Propolis is a unique natural adhesive biomass of structurally variable and biologically active metabolites that exert remarkable health benefits. Moreover, combination drug therapy has become a promising pharmacotherapeutic strategy directed for reformulating existing drugs into new combination entities with potentiating therapeutic impacts. In this study, computer-aided molecular docking and MD simulations accompanied by biochemical testing were used for mining novel pharmacologically active chemical entities from Egyptian propolis to combat hyperuricemia. Further, with a view to decrease the potential toxicity of synthetic drugs and enhance efficacy, propolis hits were subjected to combination analysis with each of allopurinol and febuxostat. More specifically, Glide docking was utilized for a structure-based virtual screening of in-house datasets comprising various Egyptian propolis metabolites. Rosmarinic acid, luteolin, techtochrysin and isoferulic acid were the most promising virtual hits.

Identifiers

PMID35425287
PMCPMC8979054
OpenAlexW4207033852

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.