Evidence map›Paper›PMID 41695418›Full record

ArticleRSC advances2026

Synthesis, multi-target evaluation and DFT analysis of 6-hydroxychromone derived hydrazones with carbonic anhydrase I-II/acetylcholinesterase inhibition and antioxidant activity.

Wajeeha Zareen, Nadeem Ahmed, Feyzi Sinan Tokali, Talha Islam, Mariya Al-Rashida, Ayşe Merve Senol, Orhan Ulucay, Ahmed Mohamed Tawfeek, Parham Taslimi, Zahid Shafiq and 1 more

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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Wajeeha ZareenInstitute of Chemical Sciences, Bahauddin Zakariya University Multan 60800 Pakistan zahidshafiq@bzu.edu.pk.
Nadeem AhmedCollege of Chemistry & Chemical Engineering, Central South University Changsha Hunan 410083 China.ORCID https://orcid.org/0000-0001-6004-0037
Feyzi Sinan TokaliDepartment of Material and Material Processing Technologies, Kars Vocational School, Kafkas University 36100 Kars Turkey.
Talha IslamDepartment of Chemistry, Forman Christian College (A Chartered University) Ferozepur Road 54600 Lahore Pakistan.
Mariya Al-RashidaDepartment of Chemistry, Forman Christian College (A Chartered University) Ferozepur Road 54600 Lahore Pakistan.
Ayşe Merve SenolDepartment of Medical Services and Techniques, Program of Medical Laboratory Techniques, University of Health Sciences 34668 Istanbul Turkey.ORCID https://orcid.org/0000-0003-3355-8222
Orhan UlucayDepartment of Bioengineering, Faculty of Engineering and Architecture, Kafkas University 36100 Kars Turkey.
Ahmed Mohamed TawfeekDepartment of Chemistry, College of Science, King Saud University P. O. Box 2455 Riyadh 11451 Saudi Arabia mislam@ksu.edu.sa.
Parham TaslimiDepartment of Biotechnology, Faculty of Science, Bartin University 74110 Bartin Turkey.
Zahid ShafiqInstitute of Chemical Sciences, Bahauddin Zakariya University Multan 60800 Pakistan zahidshafiq@bzu.edu.pk.ORCID https://orcid.org/0000-0003-4088-8297
Mohammad Shahidul IslamDepartment of Chemistry, College of Science, King Saud University P. O. Box 2455 Riyadh 11451 Saudi Arabia mislam@ksu.edu.sa.ORCID https://orcid.org/0000-0002-4612-5875

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease seems to be the result of several tumultuous processes such as cholinergic deficits associated with the abnormal metabolic status and oxidative stress that cannot be controlled effectively by single-target molecules. A complex group of agents capable of combining specific enzyme inhibition with antioxidant protection may be seen as an approach toward neuroprotection. The partial synthesis method led to the creation of a new series of chromone hydrazones (3a-p) from substituted hydrazones and 6-hydroxy-chromone. All the newly obtained hydrazones were assayed for their inhibitory activity against acetylcholinesterase (AchE) and human carbonic anhydrases (CA I and II), and their antioxidant potentials were also studied. The chromone-substituted hydrazones 3c, 3e, and 3f exhibited good inhibitory activity against AChE with IC

Identifiers

PMID41695418
PMCPMC12903877

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.