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Correction: Novel pyrimidine linked acyl thiourea derivatives as potent α-amylase and proteinase K inhibitors: design, synthesis, molecular docking and ADME studies

Hina Zamana, Aamer Saeed*a, Hammad Ismailb, Sadaf Anwaarc, Muhammad Latifd, Muhammad Zaffar Hashmie and Hesham R. El-Seedif
aDepartment of Chemistry, Quaid-I-Azam University, Islamabad, 45320, Pakistan. E-mail: asaeed@qau.edu.pk; Fax: +92-51-9064-224; Tel: +92-51-9064-2128
bDepartment of Biochemistry and Biotechnology, University of Gujrat, Gujrat 50700, Pakistan. E-mail: hammad.ismail@uog.edu.pk
cDepartment of Biological Sciences, International Islamic University, Islamabad, 45500, Pakistan. E-mail: sadaf.anwaar@iiu.edu.pk
dCentre for Genetics and Inherited Diseases (CGID), Taibah University Al-Madinah Al-Munawwarah, Kingdom of Saudi Arabia. E-mail: latifmayo@yahoo.com
eInstitute of Molecular Biology and Biotechnology, The University of Lahore, Pakistan. E-mail: muhammadzaffar.hashmi@fulbrightmail.org
fDepartment of Chemistry, Faculty of Science, Islamic University of Madinah, Madinah, 42351, Saudi Arabia. E-mail: elseedi_99@yahoo.com

Received 13th January 2025 , Accepted 13th January 2025

First published on 23rd January 2025


Abstract

Correction for ‘Novel pyrimidine linked acyl thiourea derivatives as potent α-amylase and proteinase K inhibitors: design, synthesis, molecular docking and ADME studies’ by Hina Zaman et al., RSC Adv., 2024, 14, 33235–33246, https://doi.org/10.1039/D4RA05799F.


The authors regret that one of the affiliations (affiliation e) was incorrectly shown in the original manuscript. The corrected list of affiliations is as shown here.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


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