Correction: Structure-based design, synthesis, and biological activity evaluation of chalcone–piperazine derivatives as dual AChE and MAO B inhibitors
Berkant Kurban, Begüm Nurpelin Sağlık Özkan, Derya Osmaniye, Serkan Levent, Yusuf Özkay, Zafer Asım Kaplancıklı

TL;DR
This paper corrects a previously published study on the design and testing of chalcone–piperazine compounds as inhibitors of two enzymes linked to neurological diseases.
Contribution
The correction addresses errors in the original publication to ensure scientific accuracy and reliability.
Findings
The correction clarifies details in the experimental methods and results.
It ensures the data and conclusions remain valid and trustworthy for future research.
Abstract
Correction for ‘Structure-based design, synthesis, and biological activity evaluation of chalcone–piperazine derivatives as dual AChE and MAO B inhibitors’ by Berkant Kurban et al., RSC Adv., 2025, 15, 40897–40911, https://doi.org/10.1039/D5RA05397H.
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
- —Anadolu Üniversitesi10.13039/501100008770
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Taxonomy
TopicsSynthesis and biological activity · Melanoma and MAPK Pathways · Enzyme function and inhibition
The authors regret that details of the funding information were omitted from the Acknowledgements of the original manuscript. The correct Acknowledgements are as shown below.
Acknowledgements
As the authors of this study, we thank Anadolu University Faculty of Pharmacy Central Research Laboratory (MERLAB), for their support and contributions. This study was supported by Anadolu University under the Scientific Research Projects (BAP) program, Project Code: YTT-2025-2710. Additionally, this study is a master’s thesis. YÖK Thesis number: 806986.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
