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OpenAlex Citation Counts

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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:

The 1,2,3-triazole ring as a bioisostere in medicinal chemistry
Elisa Bonandi, Michael S. Christodoulou, Gaia Fumagalli, et al.
Drug Discovery Today (2017) Vol. 22, Iss. 10, pp. 1572-1581
Open Access | Times Cited: 583

Showing 1-25 of 583 citing articles:

1,2,3-Triazole-containing hybrids as leads in medicinal chemistry: A recent overview
Khurshed Bozorov, Jiangyu Zhao, Haji Akber Aisa
Bioorganic & Medicinal Chemistry (2019) Vol. 27, Iss. 16, pp. 3511-3531
Open Access | Times Cited: 663
1,2,3-Triazole-containing hybrids as potential anticancer agents: Current developments, action mechanisms and structure-activity relationships
Zhi Xu, Shijia Zhao, Yi Liu
European Journal of Medicinal Chemistry (2019) Vol. 183, pp. 111700-111700
Closed Access | Times Cited: 422
Amide Bond Bioisosteres: Strategies, Synthesis, and Successes
Shikha Kumari, Angelica V. Carmona, Amit K. Tiwari, et al.
Journal of Medicinal Chemistry (2020) Vol. 63, Iss. 21, pp. 12290-12358
Open Access | Times Cited: 403
Cu(I)-Catalyzed Click Chemistry in Glycoscience and Their Diverse Applications
Anand K. Agrahari, Priyanka Bose, Manoj K. Jaiswal, et al.
Chemical Reviews (2021) Vol. 121, Iss. 13, pp. 7638-7956
Closed Access | Times Cited: 313
Comprehensive review on the anti-bacterial activity of 1,2,3-triazole hybrids
Bo Zhang
European Journal of Medicinal Chemistry (2019) Vol. 168, pp. 357-372
Closed Access | Times Cited: 284
The Most Common Functional Groups in Bioactive Molecules and How Their Popularity Has Evolved over Time
Peter Ertl, Eva Altmann, Jeffrey M. McKenna
Journal of Medicinal Chemistry (2020) Vol. 63, Iss. 15, pp. 8408-8418
Closed Access | Times Cited: 248
Triazole derivatives and their antiplasmodial and antimalarial activities
Xuemei Chu, Cong Wang, Wenling Wang, et al.
European Journal of Medicinal Chemistry (2019) Vol. 166, pp. 206-223
Closed Access | Times Cited: 243
CuAAC-ensembled 1,2,3-triazole-linked isosteres as pharmacophores in drug discovery: review
A. Shobha Rani, Gurjaspreet Singh, Akshpreet Singh, et al.
RSC Advances (2020) Vol. 10, Iss. 10, pp. 5610-5635
Open Access | Times Cited: 230
An overview of spirooxindole as a promising scaffold for novel drug discovery
Liming Zhou, Ren‐Yu Qu, Guang‐Fu Yang
Expert Opinion on Drug Discovery (2020) Vol. 15, Iss. 5, pp. 603-625
Closed Access | Times Cited: 229
1,2,3‐Triazole hybrids as anticancer agents: A review
Mohammad Mahboob Alam
Archiv der Pharmazie (2021) Vol. 355, Iss. 1
Closed Access | Times Cited: 214
Medicinal chemistry strategies to discover P-glycoprotein inhibitors: An update
Jinyun Dong, Zuodong Qin, Weidong Zhang, et al.
Drug Resistance Updates (2020) Vol. 49, pp. 100681-100681
Closed Access | Times Cited: 209
Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase
Chnar Kakakhan, Cüneyt Türkeş, Özcan Güleç, et al.
Bioorganic & Medicinal Chemistry (2022) Vol. 77, pp. 117111-117111
Closed Access | Times Cited: 81
Versatile Synthetic Platform for 1,2,3-Triazole Chemistry
Disha P. Vala, Ruturajsinh M. Vala, Hitendra M. Patel
ACS Omega (2022) Vol. 7, Iss. 42, pp. 36945-36987
Open Access | Times Cited: 74
1,2,3-triazole and chiral Schiff base hybrids as potential anticancer agents: DFT, molecular docking and ADME studies
Yonas Belay, Alfred Muller, Fanikie S. Mokoena, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 22
Biocompatible strategies for peptide macrocyclisation
Junming He, Pritha Ghosh, Christoph Nitsche
Chemical Science (2024) Vol. 15, Iss. 7, pp. 2300-2322
Open Access | Times Cited: 21
Multicomponent reactions (MCRs) yielding medicinally relevant rings: a recent update and chemical space analysis of the scaffolds
Mukesh Tandi, Vaibhav Sharma, B. Gopal, et al.
RSC Advances (2025) Vol. 15, Iss. 2, pp. 1447-1489
Open Access | Times Cited: 3
1,2,3‐Triazole hybrids with anti‐HIV‐1 activity
Lian‐Shun Feng, Man‐Jie Zheng, Feng Zhao, et al.
Archiv der Pharmazie (2020) Vol. 354, Iss. 1
Closed Access | Times Cited: 115
Current scenario of tetrazole hybrids for antibacterial activity
Feng Gao, Jiaqi Xiao, Gang Huang
European Journal of Medicinal Chemistry (2019) Vol. 184, pp. 111744-111744
Closed Access | Times Cited: 108
1,2,4-Triazole-quinoline/quinolone hybrids as potential anti-bacterial agents
Jingyu Zhang, Su Wang, Yanyan Ba, et al.
European Journal of Medicinal Chemistry (2019) Vol. 174, pp. 1-8
Closed Access | Times Cited: 107
Artemisinin-derived hybrids and their anticancer activity
Feng Gao, Zhou Sun, Fangong Kong, et al.
European Journal of Medicinal Chemistry (2020) Vol. 188, pp. 112044-112044
Closed Access | Times Cited: 101
Recent accomplishments on the synthetic/biological facets of pharmacologically active 1H-1,2,3-triazoles
Sumit Kumar, Bharvi Sharma, Vishu Mehra, et al.
European Journal of Medicinal Chemistry (2020) Vol. 212, pp. 113069-113069
Closed Access | Times Cited: 93
Design, Synthesis, Molecular Modeling, Anticancer Studies, and Density Functional Theory Calculations of 4-(1,2,4-Triazol-3-ylsulfanylmethyl)-1,2,3-triazole Derivatives
Adeeb Al Sheikh Ali, Daoud J. O. Khan, Arshi Naqvi, et al.
ACS Omega (2020) Vol. 6, Iss. 1, pp. 301-316
Open Access | Times Cited: 93
1,2,3-Triazole-Containing Compounds as Anti–Lung Cancer Agents: Current Developments, Mechanisms of Action, and Structure–Activity Relationship
Ting Liang, Xiangyang Sun, Wenhong Li, et al.
Frontiers in Pharmacology (2021) Vol. 12
Open Access | Times Cited: 93
Coumarin–benzimidazole hybrids: A review of developments in medicinal chemistry
Arya C. G, Ramesh Gondru, Yupeng Li, et al.
European Journal of Medicinal Chemistry (2021) Vol. 227, pp. 113921-113921
Closed Access | Times Cited: 91
Thiazolidinone-linked1,2,3-triazoles with monoterpenic skeleton as new potential anticancer agents: Design, synthesis and molecular docking studies
Ali Oubella, Az‐Eddine El Mansouri, Mourad Fawzi, et al.
Bioorganic Chemistry (2021) Vol. 115, pp. 105184-105184
Closed Access | Times Cited: 79
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