Evidence map›Paper›PMID 35607598›Full record

ArticleDrug design, development and therapy2022

Novel 2-(5-Aryl-4,5-Dihydropyrazol-1-yl)thiazol-4-One as EGFR Inhibitors: Synthesis, Biological Assessment and Molecular Docking Insights.

Tarfah Al-Warhi, Ahmed M El Kerdawy, Mohamed A Said, Amgad Albohy, Zainab M Elsayed, Nada Aljaeed, Eslam B Elkaeed, Wagdy M Eldehna, Hatem A Abdel-Aziz, Miral A Abdelmoaz

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

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  12. Discovery of novel thiazolyl-pyrazolines as dual EGFR and VEGFR-2 inhibitors endowed withJournal of enzyme inhibition and medicinal chemistry · 2022
    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 8 institutions in 2 countries.

Tarfah Al-WarhiDepartment of Chemistry, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
Ahmed M El KerdawyDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Cairo, Egypt.ORCID 0000-0003-4127-9055
Mohamed A SaidDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Egyptian Russian University, Badr City, Cairo, 11829, Egypt.ORCID 0000-0002-7937-0084
Amgad AlbohyDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, The British University in Egypt (BUE), El-Sherouk City, Cairo, 11837, Egypt.ORCID 0000-0003-3021-8767
Zainab M ElsayedScientific Research and Innovation Support Unit, Faculty of Pharmacy, Kafrelsheikh University, Kafrelsheikh, Egypt.
Nada AljaeedDepartment of Chemistry, College of Science, Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia.
Eslam B ElkaeedDepartment of Pharmaceutical Sciences, College of Pharmacy, Almaarefa University, Riyadh, 13713, Saudi Arabia.ORCID 0000-0002-2546-8035
Wagdy M EldehnaSchool of Biotechnology, Badr University in Cairo, Badr City, Cairo, 11829, Egypt.ORCID 0000-0001-6996-4017
Hatem A Abdel-AzizDepartment of Applied Organic Chemistry, National Research Center, Dokki, Giza, 12622, Egypt.ORCID 0000-0002-2606-2504
Miral A AbdelmoazDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Sinai University, Kantra, Egypt.ORCID 0000-0002-1269-7912
Kafrelsheikh University · EGPrincess Nourah bint Abdulrahman University · SAAlfaisal University · SABritish University in Egypt · EGCairo University · EGEgyptian Russian University · EGNational Research Centre · EGSinai University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Epidermal growth factor receptor (EGFR) regulates several cell functions which include cell growth, survival, multiplication, differentiation, and apoptosis. Currently, EGFR kinase inhibitors are of increasing interest as promising targeted antitumor therapeutic agents. Methods: Different thiazolyl-pyrazoline derivatives ( Results: Testing the thiazolyl pyrazoline compounds Discussion: Generally, it was observed that the tested thiazolyl pyrazolines showed more potent antiproliferative activity toward breast cancer cells T-47D than toward lung cancer cell lines A549. In particular, thiazolyl pyrazolines

Indexed as

Antineoplastic AgentsBreast NeoplasmsLung NeoplasmsCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorErbB ReceptorsErlotinib HydrochlorideFemaleHumansMolecular Docking SimulationMolecular StructureProtein Kinase InhibitorsStructure-Activity RelationshipThiazolesAntineoplastic AgentsEGFR protein, humanErbB ReceptorsErlotinib HydrochlorideProtein Kinase InhibitorsThiazolesantitumorbreast cancerEGFR inhibitorslung cancermolecular dockingpyrazolo

Identifiers

PMID35607598
PMCPMC9123247
OpenAlexW4280609152

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.