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:

Design and synthesis of novel nitrothiazolacetamide conjugated to different thioquinazolinone derivatives as anti-urease agents
Marzieh Sohrabi, Mohammad Nazari Montazer, Sara Moghadam Farid, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 24

Showing 24 citing articles:

The anti-Alzheimer potential of novel spiroindolin-1,2-diazepine derivatives as targeted cholinesterase inhibitors with modified substituents
Hormoz Pourtaher, Alireza Hasaninejad, Shahrokh Zare, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 14

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 pyridylpiperazine hybrid derivatives as urease inhibitors
Muhammad Sajid Hamid Akash, Sumera Zaib, Matloob Ahmad, et al.
Frontiers in Chemistry (2024) Vol. 12
Open Access | Times Cited: 3

Design and synthesis of new N-thioacylated ciprofloxacin derivatives as urease inhibitors with potential antibacterial activity
Keyvan Pedrood, Homa Azizian, Mohammad Nazari Montazer, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 17

Synthesis and biological evaluation of 2-nitrocinnamaldehyde derived thiosemicarbazones as urease inhibitors
Muhammad Islam, Ajmal Khan, Majid Khan, et al.
Journal of Molecular Structure (2023) Vol. 1284, pp. 135387-135387
Closed Access | Times Cited: 9

New thioxothiazolidinyl-acetamides derivatives as potent urease inhibitors: design, synthesis, in vitro inhibition, and molecular dynamic simulation
Navid Dastyafteh, Milad Noori, Mohammad Nazari Montazer, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 8

An overview of potential algae-derived bioactive compounds against urease-positive microorganisms
Najmeh Oliyaei, Mohammad Hashem Hashempur, Kamiar Zomorodian, et al.
Algal Research (2023) Vol. 77, pp. 103372-103372
Closed Access | Times Cited: 5

Synthesis, Urease Inhibition, Molecular Docking, and Optical Analysis of a Symmetrical Schiff Base and Its Selected Metal Complexes
Samuel Bonne, Muhammad Saleem, Muhammad Asif Hanif, et al.
Molecules (2024) Vol. 29, Iss. 20, pp. 4899-4899
Open Access | Times Cited: 1

Identification of (N-aryl-N-arylsulfonyl)aminoacetohydroxamic acids as novel urease inhibitors and the mechanism exploration
Suya Li, Yan Zhang, Yining Wang, et al.
Bioorganic Chemistry (2022) Vol. 130, pp. 106275-106275
Closed Access | Times Cited: 9

New solid phase methodology for the synthesis of biscoumarin derivatives: experimental and in silico approaches
Elham Zarenezhad, Mohammad Nazari Montazer, Masoumeh Tabatabaee, et al.
BMC Chemistry (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 8

Computational Strategies Targeting Inhibition of Helicobacter pylori and Cryptococcus neoformans Ureases
Marciéli Fábris, Nailton M. Nascimento-Júnior, Marcelle de Lima Ferreira Bispo, et al.
Current Pharmaceutical Design (2023) Vol. 29, Iss. 10, pp. 777-792
Closed Access | Times Cited: 4

N -Arylacetamide derivatives of methyl 1,2-benzothiazine-3-carboxylate as potential drug candidates for urease inhibition
Sajila Hina, Sumera Zaib, Maliha Uroos, et al.
Royal Society Open Science (2023) Vol. 10, Iss. 4
Open Access | Times Cited: 3

Urease
Ilaria D’Agostino, Simone Carradori
Elsevier eBooks (2023), pp. 393-410
Closed Access | Times Cited: 3

Synthesis, molecular docking, and cytotoxicity of quinazolinone and dihydroquinazolinone derivatives as cytotoxic agents
Fahimeh Taayoshi, Aida Iraji, Ali Moazzam, et al.
BMC Chemistry (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 6

A Facile, One-pot, and Green Method for Synthesis of 2-Aryl-3-(Phenylamino)Dihydroquinazolin-4(1 H )-One Derivatives Using Sodium Lauryl Sulfate (SLS) in Aqueous Media at the Room Temperature
Sara Moghadam Farid, Ali Moazzam, Keyvan Pedrood, et al.
Polycyclic aromatic compounds (2023) Vol. 44, Iss. 2, pp. 981-993
Closed Access | Times Cited: 2

Norfloxacin Derivatives as DNA Gyrase and Urease Inhibitors: Synthesis, Biological Evaluation and Molecular Docking
Breena Awan, Mohsin Abbas Khan, Irshad Ahmad, et al.
Future Medicinal Chemistry (2023) Vol. 15, Iss. 23, pp. 2181-2194
Closed Access | Times Cited: 2

Synthesis, urease inhibitory and anticancer evaluation of glucosamine-sulfonylurea conjugates
Ghadeer A. R. Y. Suaifan, Mayadah B. Shehadeh, Dua’a M. Tahboub, et al.
Medicinal Chemistry Research (2024) Vol. 33, Iss. 4, pp. 663-676
Closed Access

Benzimidazole-acrylonitrile hybrid derivatives act as potent urease inhibitors with possible fungicidal activity
Ebrahim Saeedian Moghadam, Abdullah M. Al‐Sadi, Mahdis Sadeghi Moghadam, et al.
Future Medicinal Chemistry (2024), pp. 1-18
Closed Access

Exploration of thiazine Schiff bases as promising urease inhibitors: Design, synthesis, enzyme inhibition, kinetic analysis, ADME/T evaluation, and molecular docking studies
Yousaf Khan, Mehwish Solangi, Khalid Mohammed Khan, et al.
International Journal of Biological Macromolecules (2024) Vol. 281, pp. 136361-136361
Closed Access

Ugi Bis‐Amide Derivatives as Tyrosinase Inhibitor; Synthesis, Biology Assessment, and in Silico Analysis
Faeze Yousefnejad, Aida Iraji, Reyhaneh Sabourian, et al.
Chemistry & Biodiversity (2022) Vol. 20, Iss. 1
Closed Access | Times Cited: 3

Design, synthesis, and biological studies of the new cysteine-N-arylacetamide derivatives as a potent urease inhibitor
Mohammad Nazari Montazer, Mehdi Asadi, Fatemeh Moradkhani, et al.
Naunyn-Schmiedeberg s Archives of Pharmacology (2023) Vol. 397, Iss. 1, pp. 305-315
Open Access | Times Cited: 1

Structure-based drug discovery and antimicrobial activity of ciprofloxacin‐grafted Ugi adducts
Behnam Tahmasebi, Aida Iraji, Maedeh Sherafati, et al.
Journal of Biomolecular Structure and Dynamics (2022) Vol. 41, Iss. 17, pp. 8165-8174
Closed Access | Times Cited: 1

Design, synthesis, and biological studies of the new cysteine-N-arylacetamide derivatives as potent urease inhibitor
Mohammad Nazari Montazer, Mehdi Asadi, Fatemeh Moradkhani, et al.
Research Square (Research Square) (2022)
Open Access

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