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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:

A decade of tail-approach based design of selective as well as potent tumor associated carbonic anhydrase inhibitors
Amit Kumar, Kiran Siwach, Claudiu T. Supuran, et al.
Bioorganic Chemistry (2022) Vol. 126, pp. 105920-105920
Closed Access | Times Cited: 55

Showing 1-25 of 55 citing articles:

A simple yet multifaceted 90 years old, evergreen enzyme: Carbonic anhydrase, its inhibition and activation
Claudiu T. Supuran
Bioorganic & Medicinal Chemistry Letters (2023) Vol. 93, pp. 129411-129411
Closed Access | Times Cited: 60
Novel beta-lactam substituted benzenesulfonamides: in vitro enzyme inhibition, cytotoxic activity and in silico interactions
Özcan Güleç, Cüneyt Türkeş, Mustafa Arslan, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 12, pp. 6359-6377
Closed Access | Times Cited: 49
Carbonic anhydrase IX: An atypical target for innovative therapies in cancer
Roberto Ronca, Claudiu T. Supuran
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer (2024) Vol. 1879, Iss. 4, pp. 189120-189120
Open Access | Times Cited: 19
Anti-obesity carbonic anhydrase inhibitors: challenges and opportunities
Claudiu T. Supuran
Journal of Enzyme Inhibition and Medicinal Chemistry (2022) Vol. 37, Iss. 1, pp. 2478-2488
Open Access | Times Cited: 46
Click chemistry approaches for developing carbonic anhydrase inhibitors and their applications
Andrea Angeli, Claudiu T. Supuran
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 21
Tumor associated carbonic anhydrase inhibitors: Rational approaches, design strategies, structure activity relationship and mechanistic insights
Sridhar Goud Nerella, Pavitra S. Thacker, Mohammed Arifuddin, et al.
European Journal of Medicinal Chemistry Reports (2024) Vol. 10, pp. 100131-100131
Open Access | Times Cited: 11
Design and synthesis of 6-arylpyridine-tethered sulfonamides as novel selective inhibitors of carbonic anhydrase IX with promising antitumor features toward the human colorectal cancer
Wagdy M. Eldehna, Eslam Essam Mohammed, Ghada H. Al-Ansary, et al.
European Journal of Medicinal Chemistry (2023) Vol. 258, pp. 115538-115538
Closed Access | Times Cited: 17
Targeting carbonic anhydrases for the management of hypoxic metastatic tumors
Claudiu T. Supuran
Expert Opinion on Therapeutic Patents (2023) Vol. 33, Iss. 11, pp. 701-720
Closed Access | Times Cited: 17
Multi- and poly-pharmacology of carbonic anhydrase inhibitors
Claudiu T. Supuran
Pharmacological Reviews (2024) Vol. 77, Iss. 1, pp. 100004-100004
Closed Access | Times Cited: 6
Benzenesulfonamide decorated dihydropyrimidin(thi)ones: carbonic anhydrase profiling and antiproliferative activity
Hakan Aslan, G. RENZI, Andrea Angeli, et al.
RSC Medicinal Chemistry (2024) Vol. 15, Iss. 6, pp. 1929-1941
Open Access | Times Cited: 5
Sulfonamides as anticancer agents: A brief review on sulfonamide derivatives as inhibitors of various proteins overexpressed in cancer
Khaled Elsayad, Ghada F. Elmasry, Sally Tarek Mahmoud, et al.
Bioorganic Chemistry (2024) Vol. 147, pp. 107409-107409
Closed Access | Times Cited: 5
Design, Synthesis, Anticancer Screening, and Mechanistic Study of Spiro-N-(4-sulfamoyl-phenyl)-1,3,4-thiadiazole-2-carboxamide Derivatives
Ahmed M. M. El‐Saghier, Hamada H. H. Mohammed, Sherif A. Maher, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 2, pp. 863-863
Open Access
Predicting Carbonic Anhydrase Binding Affinity: Insights from QM Cluster Models
Mackenzie Taylor, Haedam Mun, Junming Ho
The Journal of Physical Chemistry B (2025)
Closed Access
Carbonic anhydrase inhibitors: Structural insights and therapeutic potential
Priti Singh, Mohammed Arifuddin, Claudiu T. Supuran, et al.
Bioorganic Chemistry (2025), pp. 108224-108224
Closed Access
Dual targeting carbonic anhydrase inhibitors as promising therapeutic approach: a structural overview
Katia D’Ambrosio, Anna Di Fiore, Emma Langella
Frontiers in Molecular Biosciences (2025) Vol. 12
Open Access
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
Latest Advances in Specific Inhibition of Tumor-Associated Carbonic Anhydrases
Claudiu T. Supuran
Future Medicinal Chemistry (2023) Vol. 15, Iss. 1, pp. 5-7
Closed Access | Times Cited: 14
PET radiotracers and fluorescent probes for imaging human carbonic anhydrase IX and XII in hypoxic tumors
Sridhar Goud Nerella, Priti Singh, Pavitra S. Thacker, et al.
Bioorganic Chemistry (2023) Vol. 133, pp. 106399-106399
Closed Access | Times Cited: 13
An asiatic acid derived trisulfamate acts as a nanomolar inhibitor of human carbonic anhydrase VA
Toni C. Denner, Niels V. Heise, Immo Serbian, et al.
Steroids (2024) Vol. 205, pp. 109381-109381
Open Access | Times Cited: 3
Isosteviol – A new scaffold for the synthesis of carbonic anhydrase II inhibitors
Toni C. Denner, Niels V. Heise, René Csük
Results in Chemistry (2024) Vol. 7, pp. 101426-101426
Open Access | Times Cited: 3
Multiple Binding Modes of Inhibitors to Human Carbonic Anhydrases: An Update on the Design of Isoform-Specific Modulators of Activity
Katia D’Ambrosio, Anna Di Fiore, Vincenzo Alterio, et al.
Chemical Reviews (2024)
Closed Access | Times Cited: 3
Small Structural Differences Govern the Carbonic Anhydrase II Inhibition Activity of Cytotoxic Triterpene Acetazolamide Conjugates
Toni C. Denner, Niels V. Heise, Julian Zacharias, et al.
Molecules (2023) Vol. 28, Iss. 3, pp. 1009-1009
Open Access | Times Cited: 8
Derivatives of 4-methyl-1,2,3-benzoxathiazine 2,2-dioxide as selective inhibitors of human carbonic anhydrases IX and XII over the cytosolic isoforms I and II
Jekaterīna Ivanova, Morteza Abdoli, Alessio Nocentini, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 8
Design and Synthesis of Pyrazole Carboxamide Derivatives as Selective Cholinesterase and Carbonic Anhydrase Inhibitors: Molecular Docking and Biological Evaluation
Mustafa Durgun, Süleyman Akocak, Nebih Lolak, et al.
Chemistry & Biodiversity (2023) Vol. 21, Iss. 2
Closed Access | Times Cited: 8
Sulfonamide‐incorporated bis(α‐aminophosphonates) as promising carbonic anhydrase inhibitors: Design, synthesis, biological evaluation, and X‐ray crystallographic studies
Marjan Sobati, Morteza Abdoli, Andrea Angeli, et al.
Archiv der Pharmazie (2024) Vol. 357, Iss. 7
Closed Access | Times Cited: 2
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