Evidence map›Paper›PMID 35956848›Full record

ArticleMolecules (Basel, Switzerland)2022

Novel 1,3-Thiazole Analogues with Potent Activity against Breast Cancer: A Design, Synthesis, In Vitro, and In Silico Study.

Manar G Salem, Dina M Abu El-Maaty, Yassmina I Mohey El-Deen, Basem H Elesawy, Ahmad El Askary, Asmaa Saleh, Essa M Saied, Mohammed El Behery

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.8field-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

25 citing papers in PubMed, 54 citations in OpenAlex.

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  14. Thiazolo-pyridopyrimidines: AnBioImpacts : BI · 2024
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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

8 authors at 4 institutions in 3 countries.

Manar G SalemPharmaceutical Organic Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
Dina M Abu El-MaatyBiochemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 415222, Egypt.
Yassmina I Mohey El-DeenPharmaceutical Organic Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
Basem H ElesawyDepartment of Pathology, College of Medicine, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Ahmad El AskaryDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Asmaa SalehDepartment of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.
Essa M SaiedChemistry Department, Faculty of Science, Suez Canal University, Ismailia 41522, Egypt.ORCID 0000-0002-7342-6200
Mohammed El BeheryThe Division of Biochemistry, Chemistry Department, Faculty of Science, Port Said University, Port Said 42526, Egypt.ORCID 0000-0002-3120-7149
Suez Canal University · EGTaif University · SAPort Said University · EGPrincess Nourah bint Abdulrahman University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most common cancer in women, responsible for over half a million deaths in 2020. Almost 75% of FDA-approved drugs are mainly nitrogen- and sulfur-containing heterocyclic compounds, implying the importance of such compounds in drug discovery. Among heterocycles, thiazole-based heterocyclic compounds have demonstrated a broad range of pharmacological activities. In the present study, a novel set of 1,3-thiazole derivatives was designed and synthesized based on the coupling of acetophenone derivatives, and phenacyl bromide was substituted as a key reaction step. The activity of synthesized compounds was screened against the proliferation of two breast cancer cell lines (MCF-7 and MDA-MB-231). Almost all compounds exhibited a considerable antiproliferative activity toward the breast cancer cells as compared to staurosporine, with no significant cytotoxicity toward the epithelial cells. Among the synthesized compounds, compound

Indexed as

Antineoplastic AgentsBreast NeoplasmsCell ProliferationDrug DesignDrug Screening Assays, AntitumorFemaleHumansMolecular Docking SimulationMolecular StructureStaurosporineStructure-Activity RelationshipThiazolesVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2Antineoplastic AgentsStaurosporineThiazolesVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-21,3-thiazole2-hydrazinyl-1,3-thiazoleanticancer activityantiproliferationapoptosisbreast cancercell cycle arrestmolecular dockingVEGFR-2 kinase activity

Identifiers

PMID35956848
PMCPMC9370021
OpenAlexW4289346862

What OpenQuestion holds

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LicenceCC BY
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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.