Evidence map›Paper›PMID 38803909›Full record

ReviewHeliyon2024

Various synthesis and biological evaluation of some tri -tetra-substituted imidazoles derivatives: A review.

Abdeljalil Hamdi, Walid Daoudi, Mohamed Aaddouz, Mohamed Azzouzi, Hassan Amhamdi, Abdellah Elyoussfi, Abdelmalik El Aatiaoui, Dakeshwar Kumar Verma, Mohamed Abboud, M'hamed Ahari

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
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.

Abdeljalil HamdiApplied Chemistry Research Unit, FSTH, Abdelmalek Essaâdi University, AL Hoceima, Tetouan, Morocco.
Walid DaoudiLaboratory of Molecular Chemistry, Materials and Environment (LCM2E), Departement of Chemistry, Multidisciplinary Faculty of Nador, University Mohamed I, 60700 Nador, Morocco.
Mohamed AaddouzLaboratoire de chimie analytique appliquée, matériaux et environnement (LC2AME), Faculté des Sciences, B.P. 717, 60000 Oujda, Morocco.
Mohamed AzzouziLaboratory of Molecular Chemistry, Materials and Environment (LCM2E), Departement of Chemistry, Multidisciplinary Faculty of Nador, University Mohamed I, 60700 Nador, Morocco.
Hassan AmhamdiApplied Chemistry Research Unit, FSTH, Abdelmalek Essaâdi University, AL Hoceima, Tetouan, Morocco.
Abdellah ElyoussfiLaboratoire de chimie analytique appliquée, matériaux et environnement (LC2AME), Faculté des Sciences, B.P. 717, 60000 Oujda, Morocco.
Abdelmalik El AatiaouiLaboratory of Molecular Chemistry, Materials and Environment (LCM2E), Departement of Chemistry, Multidisciplinary Faculty of Nador, University Mohamed I, 60700 Nador, Morocco.
Dakeshwar Kumar VermaDepartment of Chemistry, Government Digvijay Autonomous Postgraduate College, Rajnandgaon, Chhattisgarh-491441, India.
Mohamed AbboudCatalysis Research Group (CRG), Department of Chemistry, College of Science, King Khalid University, Abha 61413, Saudi Arabia.
M'hamed AhariApplied Chemistry Research Unit, FSTH, Abdelmalek Essaâdi University, AL Hoceima, Tetouan, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The imidazole nucleus represents a significant group of heterocyclic molecules with diverse significance in the modern world due to its exploration potential and various pharmacological applications. The relevance of imidazole and its derivatives has gained popularity in recent years, especially in the production of commercial drugs and the treatment of various conditions. The imidazole nucleus is present in many natural compounds and widely distributed in essential amino acids, such as l-histidine, whose derivatives exhibit powerful pharmacological properties. In this review, we delve into the historical timeline and development of synthetic pathways for tri- and tetra-substituted imidazoles used in the renowned

Indexed as

Pharmacological applicationsPreclinical approachesRadziszewski reactionTri-tetra-substituted imidazole

Identifiers

PMID38803909
PMCPMC11128531

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.