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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:

Synthesis, characterization and biological evaluation of tertiary sulfonamide derivatives of pyridyl-indole based heteroaryl chalcone as potential carbonic anhydrase IX inhibitors and anticancer agents
Mudasir Nabi Peerzada, Parvez Κhan, Kamal Ahmad, et al.
European Journal of Medicinal Chemistry (2018) Vol. 155, pp. 13-23
Closed Access | Times Cited: 85

Showing 1-25 of 85 citing articles:

Sulfonamide derivatives as multi-target agents for complex diseases
Sinem Apaydın, Marianna Török
Bioorganic & Medicinal Chemistry Letters (2019) Vol. 29, Iss. 16, pp. 2042-2050
Closed Access | Times Cited: 191
Rosmarinic Acid Exhibits Anticancer Effects via MARK4 Inhibition
Saleha Anwar, Anas Shamsi, Mohd Shahbaaz, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 142
Sulfonamide derivatives as potential anti-cancer agents and their SARs elucidation
Yichao Wan, Guoqing Fang, Hongjuan Chen, et al.
European Journal of Medicinal Chemistry (2021) Vol. 226, pp. 113837-113837
Closed Access | Times Cited: 136
Chalcone: A Promising Bioactive Scaffold in Medicinal Chemistry
Gayathri Rajendran, Deepu Bhanu, Baladhandapani Aruchamy, et al.
Pharmaceuticals (2022) Vol. 15, Iss. 10, pp. 1250-1250
Open Access | Times Cited: 70
Pharmacotherapeutics Applications and Chemistry of Chalcone Derivatives
Jagjit Singh Dhaliwal, Said Moshawih, Khang Wen Goh, et al.
Molecules (2022) Vol. 27, Iss. 20, pp. 7062-7062
Open Access | Times Cited: 70
The importance of indole and azaindole scaffold in the development of antitumor agents
Yu Han, Wei Dong, Qunqun Guo, et al.
European Journal of Medicinal Chemistry (2020) Vol. 203, pp. 112506-112506
Closed Access | Times Cited: 130
Chalcone hybrids as potential anticancer agents: Current development, mechanism of action, and structure‐activity relationship
Feng Gao, Gang Huang, Jiaqi Xiao
Medicinal Research Reviews (2020) Vol. 40, Iss. 5, pp. 2049-2084
Closed Access | Times Cited: 104
Design and development of Isatin-triazole hydrazones as potential inhibitors of microtubule affinity-regulating kinase 4 for the therapeutic management of cell proliferation and metastasis
Babita Aneja, Nashrah Sharif Khan, Parvez Κhan, et al.
European Journal of Medicinal Chemistry (2018) Vol. 163, pp. 840-852
Closed Access | Times Cited: 85
Recent developments in biological aspects of chalcones: the odyssey continues
Anu Rani, Amit Ȧnand, Kewal Kumar, et al.
Expert Opinion on Drug Discovery (2019) Vol. 14, Iss. 3, pp. 249-288
Closed Access | Times Cited: 80
Medicinal attributes of pyridine scaffold as anticancer targeting agents
Esraa A. Mohamed, Nasser S. M. Ismail, Mohamed Hagras, et al.
Future Journal of Pharmaceutical Sciences (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 61
Carbonic anhydrase IX: A tumor acidification switch in heterogeneity and chemokine regulation
Aarfa Queen, Humaira Naaz Bhutto, Mohd Yousuf, et al.
Seminars in Cancer Biology (2022) Vol. 86, pp. 899-913
Closed Access | Times Cited: 51
Identification of α-Mangostin as a Potential Inhibitor of Microtubule Affinity Regulating Kinase 4
Parvez Κhan, Aarfa Queen, Taj Mohammad, et al.
Journal of Natural Products (2019) Vol. 82, Iss. 8, pp. 2252-2261
Closed Access | Times Cited: 73
Indole chalcones: Design, synthesis, in vitro and in silico evaluation against Mycobacterium tuberculosis
Deepthi Ramesh, Annu Joji, Balaji Gowrivel Vijayakumar, et al.
European Journal of Medicinal Chemistry (2020) Vol. 198, pp. 112358-112358
Closed Access | Times Cited: 65
Deciphering the key heterocyclic scaffolds in targeting microtubules, kinases and carbonic anhydrases for cancer drug development
Mudasir Nabi Peerzada, Ernest Hamel, Ruoli Bai, et al.
Pharmacology & Therapeutics (2021) Vol. 225, pp. 107860-107860
Closed Access | Times Cited: 53
Design, synthesis and biological evaluation of sulfamoylphenyl-quinazoline derivatives as potential EGFR/CAIX dual inhibitors
Bin Zhang, Zhikun Liu, Shengjin Xia, et al.
European Journal of Medicinal Chemistry (2021) Vol. 216, pp. 113300-113300
Closed Access | Times Cited: 45
Design, synthesis and in silico insights of novel 1,2,3-triazole benzenesulfonamide derivatives as potential carbonic anhydrase IX and XII inhibitors with promising anticancer activity
Marwa M. Abdelhakeem, Martha M. Morcoss, Dina Hanna, et al.
Bioorganic Chemistry (2024) Vol. 144, pp. 107154-107154
Closed Access | Times Cited: 6
Probing the Inhibition of Microtubule Affinity Regulating Kinase 4 by N-Substituted Acridones
Maria Voura, Parvez Κhan, Savvas Thysiadis, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 53
Synthesis and SAR studies of novel 1,2,4-oxadiazole-sulfonamide based compounds as potential anticancer agents for colorectal cancer therapy
Farheen Shamsi, Phool Hasan, Aarfa Queen, et al.
Bioorganic Chemistry (2020) Vol. 98, pp. 103754-103754
Closed Access | Times Cited: 39
A Review of the Therapeutic Importance of Indole Scaffold in Drug Discovery
Nishith Teraiya, Khushbu Agrawal, Tarun M Patel, et al.
Current Drug Discovery Technologies (2023) Vol. 20, Iss. 6
Closed Access | Times Cited: 12
Thienopyrimidine–Chalcone Hybrid Molecules Inhibit Fas-Activated Serine/Threonine Kinase: An Approach To Ameliorate Antiproliferation in Human Breast Cancer Cells
Nashrah Sharif Khan, Parvez Κhan, Mohammad Fawad Ansari, et al.
Molecular Pharmaceutics (2018) Vol. 15, Iss. 9, pp. 4173-4189
Closed Access | Times Cited: 41
Novel tertiary sulfonamide derivatives containing benzimidazole moiety as potent anti-gastric cancer agents: Design, synthesis and SAR studies
Jiansong, Qiu-Lei Gao, Bowen Wu, et al.
European Journal of Medicinal Chemistry (2019) Vol. 183, pp. 111731-111731
Closed Access | Times Cited: 41
Design, synthesis & biological evaluation of ferulic acid-based small molecule inhibitors against tumor-associated carbonic anhydrase IX
Babita Aneja, Aarfa Queen, Parvez Κhan, et al.
Bioorganic & Medicinal Chemistry (2020) Vol. 28, Iss. 9, pp. 115424-115424
Closed Access | Times Cited: 33
Novel 3-(6-methylpyridin-2-yl)coumarin-based chalcones as selective inhibitors of cancer-related carbonic anhydrases IX and XII endowed with anti-proliferative activity
Haytham O. Tawfik, Moataz A. Shaldam, Alessio Nocentini, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2022) Vol. 37, Iss. 1, pp. 1043-1052
Open Access | Times Cited: 20
Discovery of Novel Hydroxyimine-Tethered Benzenesulfonamides as Potential Human Carbonic Anhydrase IX/XII Inhibitors
Mudasir Nabi Peerzada, Daniela Vullo, Niccolò Paoletti, et al.
ACS Medicinal Chemistry Letters (2023) Vol. 14, Iss. 6, pp. 810-819
Open Access | Times Cited: 10
Discovery of 1,2,3-triazole incorporated indole-piperazines as potent antitubercular agents: Design, synthesis, in vitro biological evaluation, molecular docking and ADME studies
Rajkumar Reddyrajula, Umadevi Etikyala, Vijjulatha Manga, et al.
Bioorganic & Medicinal Chemistry (2023) Vol. 98, pp. 117562-117562
Closed Access | Times Cited: 10
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