
OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Design, synthesis, and biological investigation of selective human carbonic anhydrase II, IX, and XII inhibitors using 7-aryl/heteroaryl triazolopyrimidines bearing a sulfanilamide scaffold
Romeo Romagnoli, Tiziano De Ventura, Stefano Manfredini, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 4
Romeo Romagnoli, Tiziano De Ventura, Stefano Manfredini, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 4
Showing 4 citing articles:
Development of novel amino-benzenesulfonamide derivatives and their analogues as carbonic anhydrase inhibitors: Design, synthesis, anticancer activity assessment, and pharmacokinetic studies using UPLC-MS/MS
Khaled Elsayad, Ghada F. Elmasry, Sally Tarek Mahmoud, et al.
Bioorganic Chemistry (2025), pp. 108335-108335
Closed Access
Khaled Elsayad, Ghada F. Elmasry, Sally Tarek Mahmoud, et al.
Bioorganic Chemistry (2025), pp. 108335-108335
Closed Access
Synthesis of novel 1,2,3-triazole-tethered N-acyl hydrazones as a new class of carbonic anhydrase II inhibitors: In vitro and in silico potentials
Noor Fatima, Aamer Saeed, Saeed Ullah, et al.
Bioorganic Chemistry (2024) Vol. 153, pp. 107822-107822
Closed Access | Times Cited: 2
Noor Fatima, Aamer Saeed, Saeed Ullah, et al.
Bioorganic Chemistry (2024) Vol. 153, pp. 107822-107822
Closed Access | Times Cited: 2
New Structural Features of Isatin Dihydrothiazole Hybrids for Selective Carbonic Anhydrase Inhibitors
Daniela Secci, Simona Distinto, Alessia Onali, et al.
ACS Medicinal Chemistry Letters (2024) Vol. 15, Iss. 11, pp. 1860-1865
Closed Access | Times Cited: 1
Daniela Secci, Simona Distinto, Alessia Onali, et al.
ACS Medicinal Chemistry Letters (2024) Vol. 15, Iss. 11, pp. 1860-1865
Closed Access | Times Cited: 1
An overview of the most used synthetic pathways of 1,2,4-triazolo[1,5-a]pyrimidines
Mohamed Nabil Zedan, Mai E. Shoman, Mohamed Abdel‐Aziz, et al.
Results in Chemistry (2024) Vol. 12, pp. 101903-101903
Open Access | Times Cited: 1
Mohamed Nabil Zedan, Mai E. Shoman, Mohamed Abdel‐Aziz, et al.
Results in Chemistry (2024) Vol. 12, pp. 101903-101903
Open Access | Times Cited: 1
Exploring heterocyclic scaffolds in carbonic anhydrase inhibition: a decade of structural and therapeutic insights
Nafeesa Naeem, Amina Sadiq, Mohamed I. A. Othman, et al.
RSC Advances (2024) Vol. 14, Iss. 48, pp. 35769-35970
Open Access
Nafeesa Naeem, Amina Sadiq, Mohamed I. A. Othman, et al.
RSC Advances (2024) Vol. 14, Iss. 48, pp. 35769-35970
Open Access