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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:

An overview on the synthetic urease inhibitors with structure-activity relationship and molecular docking
Wei Yang, Qianqian Feng, Zhiyun Peng, et al.
European Journal of Medicinal Chemistry (2022) Vol. 234, pp. 114273-114273
Closed Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

Flavonoids and related privileged scaffolds as potential urease inhibitors: a review
Munirah M. Al‐Rooqi, Ehsan Ullah Mughal, Qandeel Alam Raja, et al.
RSC Advances (2023) Vol. 13, Iss. 5, pp. 3210-3233
Open Access | Times Cited: 24
DNA protection, molecular docking, enzyme inhibition and enzyme kinetic studies of 1,5,9-epideoxyloganic acid isolated fromNepeta aristatawith bio-guided fractionation
Yunus Başar, Semiha Yenigün, Yaşar İpek, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 17, pp. 9235-9248
Closed Access | Times Cited: 19
A Small-Molecule Inhibitor of Gut Bacterial Urease Protects the Host from Liver Injury
Khyle C. Richards-Corke, Yindi Jiang, Vladimir Yeliseyev, et al.
ACS Chemical Biology (2025)
Closed Access
Design, synthesis, in vitro evaluation, and molecular dynamics simulation studies of novel coumarin-acetohydrazide Schiff base derivatives as urease enzyme inhibitors
Mohammad Reza Azimi, Hassan Sepehrmansourie, Ahmad Ebadi, et al.
Medicinal Chemistry Research (2025)
Closed Access
Synthesis and Evaluation of Novel Ebselen Derivatives as Urease Inhibitors for Combating Helicobacter pylori Infections
Weilong Cao, Feng Jin, Binzhuo Liu, et al.
European Journal of Medicinal Chemistry (2025) Vol. 287, pp. 117359-117359
Closed Access
Novel Sulfamide-Hydroxamic Acids Containing Piperazine/Piperidine Segment as Potent Urease Inhibitors: Synthesis, Biological Evaluation, Kinetics and Molecular Docking Studies
Yao Zeng, Wan‐Qing Song, Liang-Chao Yuan, et al.
(2025)
Closed Access
Phenolic profiles, antioxidant, antiquorum sensing, antibiofilm and enzyme inhibitory activities of selected Acacia species collected from Benin
Koudoro Yaya Alain, Alfred Ngenge Tamfu, Selçuk Küçükaydın, et al.
LWT (2022) Vol. 171, pp. 114162-114162
Open Access | Times Cited: 31
Exploring Recent Updates on Molecular Docking: Types, Method, Application, Limitation & Future Prospects
Mahendra Kumar Sahu, Amit Kumar Nayak, Bisrat Hailemeskel, et al.
International Journal Of Pharmaceutical Research And Allied Sciences (2024) Vol. 13, Iss. 2, pp. 24-40
Closed Access | Times Cited: 5
Use of hybrid molecular simulation techniques for systematic analysis of polyphenols as promising therapeutic agent against SARS-CoV-2
Shabbir Muhammad, Shafiq urRehman, Maimoona Zia, et al.
Journal of Molecular Structure (2024) Vol. 1305, pp. 137744-137744
Closed Access | Times Cited: 4
Synergizing structure and function: Cinnamoyl hydroxamic acids as potent urease inhibitors
L. Viana, Giovanna M. Naves, Isabela G. Medeiros, et al.
Bioorganic Chemistry (2024) Vol. 146, pp. 107247-107247
Closed Access | Times Cited: 4
Urease inhibition and molecular docking studies on transition metal complexes of ligands derived from barbituric and thiobarbituric acids
Syed Raza Shah, Majid Khan, Sobia Ahsan Halim, et al.
Applied Organometallic Chemistry (2024) Vol. 38, Iss. 6
Closed Access | Times Cited: 4
An overview: metal-based inhibitors of urease
Wei Yang, Zhiyun Peng, Guangcheng Wang
Journal of Enzyme Inhibition and Medicinal Chemistry (2022) Vol. 38, Iss. 1, pp. 361-375
Open Access | Times Cited: 21
Different barbiturate derivatives linked to aryl hydrazone moieties as urease inhibitors; design, synthesis, urease inhibitory evaluations, and molecular dynamic simulations
Marjan Mollazadeh, Homa Azizian, Azadeh Fakhrioliaei, et al.
Medicinal Chemistry Research (2023) Vol. 32, Iss. 5, pp. 930-943
Closed Access | Times Cited: 12
Synthesis and biological evaluation of triazolones/oxadiazolones as novel urease inhibitors
Yining Wang, Suya Li, Liang-Chao Yuan, et al.
Bioorganic & Medicinal Chemistry (2024) Vol. 102, pp. 117656-117656
Closed Access | Times Cited: 3
Synthesis of novel 2-mercapto-1,3,4-oxadiazole derivatives as potent urease inhibitors: In vitro and in silico investigations
Aziz Khan, Ahmed A. Elhenawy, Munir Ur Rehman, et al.
Journal of Molecular Structure (2024) Vol. 1312, pp. 138596-138596
Closed Access | Times Cited: 2
Syntheses, crystal structure, luminescent properties and Hirshfeld surface of a set of triazole-based salts
Bing-Qian Jin, Yu-Qing Song, Yin−Xue Ma, et al.
Journal of Molecular Structure (2023) Vol. 1279, pp. 134980-134980
Closed Access | Times Cited: 6
Chalcones bearing nitrogen‐containing heterocyclics as multi‐targeted inhibitors: Design, synthesis, biological evaluation and molecular docking studies
Yusuf Sıcak, Hüseyin Kekeçmuhammed, Ayşegül Karaküçük‐İyidoğan, et al.
Journal of Molecular Recognition (2023) Vol. 36, Iss. 7
Closed Access | Times Cited: 5
Ureases as drug targets in urinary tract infections
Charles E. Deutch
Elsevier eBooks (2024), pp. 297-340
Closed Access | Times Cited: 1
Antiurease Activity of Antibiotics: In Vitro, In Silico, Structure Activity Relationship, and MD Simulations of Cephalosporins and Fluoroquinolones
Misbah Aslam, Jameel Rahman, Ambar Iqbal, et al.
ACS Omega (2024) Vol. 9, Iss. 12, pp. 14005-14016
Open Access | Times Cited: 1
Synthesis, and molecular docking of thiourea derivatives as antibacterial agents targeting enzymes involved in biosynthesis of bacterial cell wall
Suzana, Nuzul Wahyuning Diyah, Rini Susanti, et al.
Pharmacy Education (2024) Vol. 24, Iss. 2, pp. 71-77
Open Access | Times Cited: 1
Inhibitory activity of catecholic phosphonic and phosphinic acids against Helicobacter pylori ureolysis
Marta Maślanka, Wojciech Tabor, Paweł Krzyżek, et al.
European Journal of Medicinal Chemistry (2023) Vol. 257, pp. 115528-115528
Open Access | Times Cited: 4
Chemical characterization, in vitro antioxidant, anti-cancer and enzyme inhibition activities of three edible mushroom species
Ebru Deveci, Gülsen Tel‐Çayan, Fatih Çayan, et al.
Journal of Food Measurement & Characterization (2023) Vol. 17, Iss. 5, pp. 5518-5533
Closed Access | Times Cited: 4
Design, Synthesis and Evaluation of Aryl‐Tailored Oxadiazole‐thiones as New Urease Inhibitors
Tuğçe Gür Maz, H. Burak Caliskan, İrfan Çapan, et al.
ChemistrySelect (2023) Vol. 8, Iss. 8
Closed Access | Times Cited: 3
Unusual short intramolecular N–H⋅⋅⋅H–C contact and weak intermolecular interactions in two N-(adamantan-1-yl)piperazine carbothioamides: Crystallography, quantum chemical study and in vitro urease inhibitory activity
Lamya H. Al-Wahaibi, Sivashanmugam Mangaiyarkarasi, Olivier Blacque, et al.
Journal of Molecular Structure (2023) Vol. 1291, pp. 136052-136052
Closed Access | Times Cited: 3
In vitro evaluation of novel mefenamic acid derivatives as potential α-glucosidase and urease inhibitors: Design, synthesis, in silico and cytotoxic studies
Saima Daud, Obaid‐ur‐Rahman Abid, Wajid Rehman, et al.
Journal of Saudi Chemical Society (2023) Vol. 27, Iss. 4, pp. 101680-101680
Open Access | Times Cited: 3
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