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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:

S-substituted 2-mercaptoquinazolin-4(3H)-one and 4-ethylbenzensulfonamides act as potent and selective human carbonic anhydrase IX and XII inhibitors
Adel S. El‐Azab, Alaa A.‐M. Abdel‐Aziz, Silvia Bua, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2020) Vol. 35, Iss. 1, pp. 733-743
Open Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

Targeting carbonic anhydrase IX and XII isoforms with small molecule inhibitors and monoclonal antibodies
Mateusz Kciuk, Adrianna Gielecińska, Somdutt Mujwar, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2022) Vol. 37, Iss. 1, pp. 1278-1298
Open Access | Times Cited: 69
Recent advances in the medicinal chemistry of carbonic anhydrase inhibitors
Shubham Kumar, Sandeep Rulhania, Shalini Jaswal, et al.
European Journal of Medicinal Chemistry (2020) Vol. 209, pp. 112923-112923
Closed Access | Times Cited: 114
Recent Advances on Quinazoline Derivatives: A Potential Bioactive Scaffold in Medicinal Chemistry
Ram Karan, Pooja Agarwal, Mukty Sinha, et al.
ChemEngineering (2021) Vol. 5, Iss. 4, pp. 73-73
Open Access | Times Cited: 64
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
Identification of thienopyrimidine derivatives tethered with sulfonamide and other moieties as carbonic anhydrase inhibitors: Design, synthesis and anti-proliferative activity
Samah Higazy, Nermin Samir, Ahmed El‐Khouly, et al.
Bioorganic Chemistry (2024) Vol. 144, pp. 107089-107089
Closed Access | Times Cited: 11
Synthesis of new sulfonamide derivatives: Investigation of their interactions with carbonic anhydrase and cholinesterase enzymes by in vitro and in silico evaluations
Muhammet Gürkan Kurban, Reşit Çakmak, Eyüp Başaran, et al.
Journal of Molecular Structure (2024) Vol. 1314, pp. 138798-138798
Closed Access | Times Cited: 5
S-Alkylated quinazolin-4(3H)-ones as dual EGFR/VEGFR-2 kinases inhibitors: design, synthesis, anticancer evaluation and docking study
Samar S. Tawfik, Abdelrahman Hamdi, Ahmed R. Ali, et al.
RSC Advances (2024) Vol. 14, Iss. 36, pp. 26325-26339
Open Access | Times Cited: 5
Remarkable utilization of quinazoline-based homosulfonamide for in vitro cytotoxic effects with triple kinase inhibition activities: cell cycle analysis and molecular docking profile
Adel S. El‐Azab, Alaa A.‐M. Abdel‐Aziz, Ahmed H. Bakheit, et al.
RSC Advances (2025) Vol. 15, Iss. 1, pp. 541-558
Open Access
A novel class of phenylpyrazolone-sulphonamides rigid synthetic anticancer molecules selectively inhibit the isoform IX of carbonic anhydrases guided by molecular docking and orbital analyses
Maan T. Khayat, Hany E. A. Ahmed, Abdelsattar M. Omar, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 41, Iss. 24, pp. 15243-15261
Closed Access | Times Cited: 14
Recent Advances in Biological Active Sulfonamide based Hybrid Compounds Part A: Two-Component Sulfonamide Hybrids
Reihane Ghomashi, Shakila Ghomashi, Hamidreza Aghaei, et al.
Current Medicinal Chemistry (2022) Vol. 30, Iss. 4, pp. 407-480
Closed Access | Times Cited: 20
Novel 2‐substituted thioquinazoline‐benzenesulfonamide derivatives as carbonic anhydrase inhibitors with potential anticancer activity
Heba T. Abdel‐Mohsen, Mohamed A. Omar, Andrea Petreni, et al.
Archiv der Pharmazie (2022) Vol. 355, Iss. 12
Closed Access | Times Cited: 17
Investigation of the carbonic anhydrase inhibitory activity of benzenesulfonamides incorporating substituted fused‐pyrimidine tails
Heba T. Abdel‐Mohsen, Andrea Petreni, Claudiu T. Supuran
Archiv der Pharmazie (2022) Vol. 355, Iss. 11
Closed Access | Times Cited: 14
Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review
Anjaneyulu Bendi, Taruna, Rajni Rajni, et al.
Archiv der Pharmazie (2024) Vol. 357, Iss. 7
Closed Access | Times Cited: 2
Design, synthesis, and carbonic anhydrase inhibition activities of Schiff bases incorporating benzenesulfonamide scaffold: Molecular docking application
Adel S. El‐Azab, Alaa A.‐M. Abdel‐Aziz, Silvia Bua, et al.
Saudi Pharmaceutical Journal (2023) Vol. 31, Iss. 12, pp. 101866-101866
Open Access | Times Cited: 7
Carbonic Anhydrase Inhibition Activities of Schiff’s Bases Based on Quinazoline-Linked Benzenesulfonamide
Adel S. El‐Azab, Alaa A.‐M. Abdel‐Aziz, Hazem A. Ghabbour, et al.
Molecules (2022) Vol. 27, Iss. 22, pp. 7703-7703
Open Access | Times Cited: 11
Synthesis, antiproliferative and enzymatic inhibition activities of quinazolines incorporating benzenesulfonamide: Cell cycle analysis and molecular modeling study
Adel S. El‐Azab, Hamad M. Alkahtani, Nawaf A. Alsaif, et al.
Journal of Molecular Structure (2023) Vol. 1278, pp. 134928-134928
Closed Access | Times Cited: 6
Application of Deep Eutectic Solvents in the Synthesis of Substituted 2-Mercaptoquinazolin-4(3H)-Ones: A Comparison of Selected Green Chemistry Methods
Mario Komar, Tatjana Gazivoda Kraljević, Igor Jerković, et al.
Molecules (2022) Vol. 27, Iss. 2, pp. 558-558
Open Access | Times Cited: 10
Synthesis, Characterization and Molecular Docking Study of Novel 1,4-Dihydropyridine Derivatives as Antimicrobial and Anticancer Agents
Fereshteh Gandomi, Karim Akbari Dilmaghani, Bakhshali Massoumi, et al.
Russian Journal of Bioorganic Chemistry (2023) Vol. 49, Iss. 5, pp. 1089-1099
Closed Access | Times Cited: 3
Green synthesis of 2‐thioxo‐4‐quinazolinones from 2‐aminobenzamide and isothiocyanates
Ngoc Binh Vo, Le Thanh Hang Nguyen, Thi Yen Tran, et al.
Vietnam Journal of Chemistry (2024) Vol. 62, Iss. S1, pp. 147-152
Open Access
Prominent Antidiabetic and Anticancer Investigation of Scrophularia deserti Extract: Integration of Experimental and Computational Approaches
Arafa Musa, Shaimaa R. Ahmed, Shaimaa Hussein, et al.
Journal of Molecular Structure (2024) Vol. 1315, pp. 138769-138769
Closed Access
Recent Advances in the Design and Synthesis of Small Molecule Carbonic Anhydrase IX Inhibitors
Peng‐Cheng Lv, Yinyi Cai, Jiayi Luo, et al.
Current Topics in Medicinal Chemistry (2022) Vol. 22, Iss. 7, pp. 550-560
Closed Access | Times Cited: 2
MOLECULAR FIELD-BASED QSAR STUDIES AND DOCKING ANALYSIS OF MERCAPTOQUINAZOLINONE BENZENE SULFONAMIDE DERIVATIVES AGAINST hCA XII
Pushparathinam Gopinath, M. K. Kathiravan
RASAYAN Journal of Chemistry (2022) Vol. 15, Iss. 01, pp. 686-699
Open Access | Times Cited: 2
Synthesis and Inhibition Activity Study of Triazinyl-Substituted Amino(alkyl)-benzenesulfonamide Conjugates with Polar and Hydrophobic Amino Acids as Inhibitors of Human Carbonic Anhydrases I, II, IV, IX, and XII
Mária Bodnár Mikulová, Dáša Kružlicová, Daniel Pecher, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 20, pp. 11283-11283
Open Access | Times Cited: 2
Synthesis and antibacterial activities of some novel hybrid compounds based on 2‐mercapto‐3‐arylquinazolin‐4(3H)‐one scaffold bearing specific coumarin
Linh Bui Thi Thuy, Phuoc Le Thien, Chi–Hien Dang, et al.
Vietnam Journal of Chemistry (2023) Vol. 61, Iss. S2, pp. 131-136
Open Access
Methyl 2-((3-(3-methoxyphenyl)-4-oxo-3,4-dihydroquinazolin-2-yl)thio)acetate
Maja Molnar, Mario Komar, Igor Jerković
Molbank (2022) Vol. 2022, Iss. 3, pp. M1434-M1434
Open Access
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