Evidence map›Paper›PMID 38500276›Full record

ArticleCurrent medicinal chemistry2025

Synthesis of Bis-thiazoles Tethered 1,4-Dihydropyridine and Pyridine Linkers

Jehan Yahia Al-Humaidi, Sayed Mohamed Riyadh, Basant Farag, Magdi Elsayed Abdelsalam Zaki, Tariq Ziyad Abolibda, Sobhi Mohamed Gomha

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Article in Current medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

5 citing papers in PubMed, 11 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 5 institutions in 2 countries.

Jehan Yahia Al-HumaidiDepartment of Chemistry, College of Science, Princess Nourah bint Abdulrahman University, P.O. BOX 84428, Riyadh 11671, Saudi Arabia.
Sayed Mohamed RiyadhDepartment of Chemistry, Faculty of Science, Cairo University, Cairo 12613, Egypt.
Basant FaragDepartment of Chemistry, Faculty of Science, Zagazig University, Zagazig 44519, Egypt.
Magdi Elsayed Abdelsalam ZakiDepartment of Chemistry, Faculty of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11623, Saudi Arabia.
Tariq Ziyad AbolibdaDepartment of Chemistry, Faculty of Science, Islamic University of Madinah, Madinah, 42351, Saudi Arabia.
Sobhi Mohamed GomhaDepartment of Chemistry, Faculty of Science, Islamic University of Madinah, Madinah, 42351, Saudi Arabia.
Islamic University of Madinah · SACairo University · EGImam Mohammad ibn Saud Islamic University · SAPrincess Nourah bint Abdulrahman University · SAZagazig University · EG

Funding

Princess Nourah Bint Abdulrahman University, Riyadh, Saudi Arabia PNURSP2023R24
6 · The paper itself

Abstract

aimIn this study, a neoteric and expedient oxidation method is applied for a variety of Hantzsch 1,4-dihydropyridine derivatives such as 1,4-dihydro- 2,6-dimethyl-3,5-diacetylpyridine, 3,5-bis-hydrazono--2,6-dimethyl-1,4-dihydropyridine, and 3,5-bis-thiazoly-2,6-dimethyl-1,4-dihydro pyridines.

methodsThis simple oxidation is based upon the

resultThe results revealed that the interaction of hydrazinylidene and thiazole as an anticancer Tyrosine Kinase inhibitor has been improved.

conclusionAdditionally, the compounds exhibiting the highest activity were assessed for their potential anticancer effects against HepG-2, MCF-7, and WI-38 cells, and the outcomes demonstrated encouraging activity against cancer.

Indexed as

Antineoplastic AgentsDihydropyridinesMolecular Docking SimulationProtein Kinase InhibitorsPyridinesReceptors, Vascular Endothelial Growth FactorThiazolesCell Line, TumorCell ProliferationHumansMolecular StructureOxidation-ReductionStructure-Activity Relationship1,4-dihydropyridineAntineoplastic AgentsDihydropyridinesProtein Kinase InhibitorspyridinePyridinesReceptors, Vascular Endothelial Growth FactorThiazoles14-dihydropyridinesanticancerhydrazonoyl halidesmolecular dockingnitrous acidOxidationSAR.VEGFR-2 inhibitors

Identifiers

PMID38500276
OpenAlexW4392876925

What OpenQuestion holds

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Registered trials

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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.