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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
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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