Evidence map›Paper›PMID 42851996›Full record

ArticleRSC advances2026

Synthesis, characterization, X-ray diffraction,

Edmore F Kangara, Thishana Singh, Phindile Khoza, Darian Naidu, Nompumelelo P Mkwananzi, Sibusiso Senzani, Oluwatoba E Oyeneyin, Manuel A Fernandes, Werner Van Zyl, Matshawandile Tukulula

Abstract read
In one paragraph

Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Edmore F KangaraMolecular Sciences Institute, School of Chemistry, University of the Witwatersrand Private Bag X3 Johannesburg 2050 South Africa kangara.edd@gmail.com.ORCID https://orcid.org/0000-0003-0541-2429
Thishana SinghDiscipline of Chemistry, School of Agriculture and Engineering, University of KwaZulu-Natal Private Bag X54001, Westville Durban 4000 South Africa TukululaM@ukzn.ac.za.ORCID https://orcid.org/0000-0003-1007-4540
Phindile KhozaDiscipline of Chemistry, School of Agriculture and Engineering, University of KwaZulu-Natal Private Bag X54001, Westville Durban 4000 South Africa TukululaM@ukzn.ac.za.
Darian NaiduHIV Pathogenesis Programme, Doris Duke Medical Research Institute, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal Durban 4001 South Africa.
Nompumelelo P MkwananziHIV Pathogenesis Programme, Doris Duke Medical Research Institute, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal Durban 4001 South Africa.
Sibusiso SenzaniSchool of Laboratory Medicine and Medical Science, College of Health Sciences, University of KwaZulu-Natal Medical School Campus Durban 4001 South Africa.
Oluwatoba E OyeneyinDepartment of Chemical and Physical Sciences, Walter Sisulu University (WSU) Private Bag X01 Mthatha Eastern Cape 4099 South Africa.
Manuel A FernandesMolecular Sciences Institute, School of Chemistry, University of the Witwatersrand Private Bag X3 Johannesburg 2050 South Africa kangara.edd@gmail.com.ORCID https://orcid.org/0000-0002-4849-5335
Werner Van ZylDiscipline of Chemistry, School of Agriculture and Engineering, University of KwaZulu-Natal Private Bag X54001, Westville Durban 4000 South Africa TukululaM@ukzn.ac.za.ORCID https://orcid.org/0000-0002-2012-8584
Matshawandile TukululaDiscipline of Chemistry, School of Agriculture and Engineering, University of KwaZulu-Natal Private Bag X54001, Westville Durban 4000 South Africa TukululaM@ukzn.ac.za.ORCID https://orcid.org/0000-0002-1844-3614

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of thiazole-2-imines (1a-1f) with unsubstituted aryl groups or aryl groups bearing methyl, methoxy, fluoro, or nitro substituents was designed using selected structural features of thiamine as inspiration. The compounds were synthesized from monosubstituted acylthioureas and

Identifiers

PMID42851996
PMCPMC13646916

What OpenQuestion holds

Textmetadata
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.