Evidence map›Paper›PMID 34103896›Full record

ArticleDrug design, development and therapy2021

Novel Phenolic Compounds as Potential Dual EGFR and COX-2 Inhibitors: Design, Semisynthesis, in vitro Biological Evaluation and in silico Insights.

Mohamed A Abdelgawad, Arafa Musa, Atiah H Almalki, Sami I Alzarea, Ehab M Mostafa, Mostafa M Hegazy, Gomaa Mostafa-Hedeab, Mohammed M Ghoneim, Della G T Parambi, Rania B Bakr and 6 more

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2021. 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
5.0field-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

13 citing papers in PubMed, 41 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

16 authors at 6 institutions in 3 countries.

Mohamed A AbdelgawadDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.ORCID 0000-0001-9035-5638
Arafa MusaDepartment of Pharmacognosy, College of Pharmacy, Jouf University, Sakaka, 72341, Saudi Arabia.ORCID 0000-0003-0979-556X
Atiah H AlmalkiDepartment of Pharmaceutical Chemistry, College of Pharmacy, Taif University, Taif, 21944, Saudi Arabia.
Sami I AlzareaDepartment of Pharmacology, College of Pharmacy, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.
Ehab M MostafaDepartment of Pharmacognosy, College of Pharmacy, Jouf University, Sakaka, 72341, Saudi Arabia.
Mostafa M HegazyDepartment of Pharmacognosy, Faculty of Pharmacy, Al-Azhar University, Cairo, 11371, Egypt.ORCID 0000-0001-8975-9424
Gomaa Mostafa-HedeabDepartment of Pharmacology, Medical College, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.
Mohammed M GhoneimDepartment of Pharmacognosy, Faculty of Pharmacy, Al-Azhar University, Cairo, 11371, Egypt.ORCID 0000-0002-9179-4373
Della G T ParambiDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.
Rania B BakrDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.
Nayef S Al-MuaikelDepartment of Chemistry, College of Science, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.
Abdullah S AlanaziDepartment of Clinical Pharmacy, College of Pharmacy, Jouf University, Sakaka, Aljouf, Saudi Arabia.ORCID 0000-0002-8120-4018
Metab AlharbiDepartment of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh, 11451, Saudi Arabia.
Waqas AhmadDrug and Herbal Research Centre, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Syed N A BukhariDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.ORCID 0000-0001-8125-7972
Mohammad M Al-SaneaDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka, Aljouf, 72341, Saudi Arabia.ORCID 0000-0002-9820-4022
Jouf University · SAAl-Azhar University · EGAlfaisal University · SAKing Saud University · SANational University of Malaysia · MYTaif University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionEpidermal growth factor receptor (EGFR) inhibition is an imperative therapeutic approach targeting various types of cancer including colorectal, lung, breast, and pancreatic cancer types. Moreover, cyclooxygenase-2 (COX-2) is frequently overexpressed in different types of cancers and has a role in the promotion of malignancy, apoptosis inhibition, and metastasis of tumor cells. Combination therapy has been emerged to improve the therapeutic benefit against cancer and curb intrinsic and acquired resistance.

methodsThree semi-synthetic series of compounds (

resultsCompounds DISCUSSION: The NMR of prepared compounds showed characteristic peaks that confirmed the structure of the target compounds. The synthesized benzoxazolyl scaffold containing compounds showed inhibitory activities for both COXs and EGFR which are consistent with the virtual docking study.

Indexed as

Drug DesignAmaranthaceaeCyclooxygenase 2Cyclooxygenase 2 InhibitorsErbB ReceptorsHumansMolecular Docking SimulationMolecular StructurePhenolsPlant ExtractsProtein Kinase InhibitorsCyclooxygenase 2Cyclooxygenase 2 InhibitorsEGFR protein, humanErbB ReceptorsPhenolsPlant ExtractsProtein Kinase Inhibitorsanticanceranti-inflammatoryBRAFkinase inhibitorsmultitarget agents

Identifiers

PMID34103896
PMCPMC8178614
OpenAlexW3170423241

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.