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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:

Identification of phenylcarbamoylazinane-1,3,4-oxadiazole amides as lipoxygenase inhibitors with expression analysis and in silico studies
Bushra Bashir, Wardah Shahid, Muhammad Ashraf, et al.
Bioorganic Chemistry (2021) Vol. 115, pp. 105243-105243
Closed Access | Times Cited: 18

Showing 18 citing articles:

Synthesis and Evaluation of 1,3,5-Triaryl-2-Pyrazoline Derivatives as Potent Dual Inhibitors of Urease and α-Glucosidase Together with Their Cytotoxic, Molecular Modeling and Drug-Likeness Studies
Rabia Mehmood, Amina Sadiq, Reem I. Alsantali, et al.
ACS Omega (2022) Vol. 7, Iss. 4, pp. 3775-3795
Open Access | Times Cited: 32
Dual COX-2/15-LOX inhibitors: A new avenue in the prevention of cancer
Ali Aliabadi, Elham Khanniri, Mohammad Mahboubi‐Rabbani, et al.
European Journal of Medicinal Chemistry (2023) Vol. 261, pp. 115866-115866
Closed Access | Times Cited: 11
Synthesis, in Vitro Cholinesterase Inhibition, Molecular Docking, DFT, and ADME Studies of Novel 1,3,4‐Oxadiazole‐2‐Thiol Derivatives
Sidra Tariq, Sadaf Mutahir, Muhammad Asim Khan, et al.
Chemistry & Biodiversity (2022) Vol. 19, Iss. 8
Closed Access | Times Cited: 16
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
Synthesis of novel oxadiazole derivatives: DFT calculations, molecular docking studies, and in vitro, in vivo evaluation of antidiabetic activity using Drosophila melanogaster model
Govinda Anjanayya, Ramesh S. Gani, Avinash K. Kudva, et al.
Journal of the Iranian Chemical Society (2024) Vol. 21, Iss. 8, pp. 2221-2237
Closed Access | Times Cited: 2
Design, Synthesis and Characterization of Strontium and Cerium-Co-Doped TiO 2 -HAp as an Efficient Nanocomposite: Investigation of Its Photocatalytic and Catalytic Applications
Alireza Esmaeilzadeh, Felora Heshmatpour
Polycyclic aromatic compounds (2023) Vol. 43, Iss. 10, pp. 9461-9478
Closed Access | Times Cited: 6
Design, synthesis, in vitro and in silico studies of naproxen derivatives as dual lipoxygenase and α-glucosidase inhibitors
Asma Sardar, Obaid‐ur‐Rahman Abid, Saima Daud, et al.
Journal of Saudi Chemical Society (2022) Vol. 26, Iss. 3, pp. 101468-101468
Open Access | Times Cited: 9
Assessing p-tolyloxy-1,3,4-oxadiazole acetamides as lipoxygenase inhibitors assisted by in vitro and in silico studies
Bushra Bashir, Naheed Riaz, Syeda Abida Ejaz, et al.
Bioorganic Chemistry (2022) Vol. 129, pp. 106144-106144
Closed Access | Times Cited: 9
Probing N-Substituted 4-(5-mercapto-4-ethyl-4H-1,2,4-triazol-3-yl)-N-phenylpiperdine-1-carboxamides as potent 15-LOX inhibitors supported with ADME, DFT calculations and molecular docking studies
Zahid Nawaz, Naheed Riaz, Muhammad Saleem, et al.
Heliyon (2024) Vol. 10, Iss. 17, pp. e35278-e35278
Open Access | Times Cited: 1
Vetting of new N-furfurylated p-chlorophenyl-1,2,4-triazole acetamides as lipoxygenase inhibitors assisted with in vitro and in silico studies
Naheed Riaz, Muhammad Yasin, Muhammad Ashraf, et al.
Journal of the Iranian Chemical Society (2023) Vol. 20, Iss. 4, pp. 977-994
Closed Access | Times Cited: 4
Exploring ibuprofen derivatives as α‐glucosidase and lipoxygenase inhibitors: Cytotoxicity and in silico studies
Saima Daud, Obaid‐ur‐Rahman Abid, Asma Sardar, et al.
Archiv der Pharmazie (2022) Vol. 355, Iss. 8
Closed Access | Times Cited: 7
Investigations of p -tolyloxy-1,3,4-oxadiazole propionamides as soybean 15-lipoxygenase inhibitors in comforting with in vitro and in silico studies
Bushra Bashir, Naheed Riaz, Syeda Abida Ejaz, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 41, Iss. 24, pp. 15549-15568
Closed Access | Times Cited: 3
Molecular hybrids of substituted phenylcarbamoylpiperidine and 1,2,4-triazole methylacetamide as potent 15-LOX inhibitors: Design, synthesis, DFT calculations and molecular docking studies
Zahid Nawaz, Naheed Riaz, Muhammad Saleem, et al.
Bioorganic Chemistry (2023) Vol. 143, pp. 106984-106984
Closed Access | Times Cited: 3
Design, synthesis, and pharmacological evaluation of indazole carboxamides of N-substituted pyrrole derivatives as soybean lipoxygenase inhibitors
Vasiliki Lavrentaki, Antonios Kousaxidis, Panagiotis Theodosis‐Nobelos, et al.
Molecular Diversity (2023)
Closed Access | Times Cited: 2
Exploration of 4-tolyl-5-(p-tolyloxymethyl)-4H-1,2,4-triazole thioethers as potent 15-LOX inhibitors supported by in vitro, in silico, MD simulation and DNA binding studies
Ambar Iqbal, Muhammad Ashraf, Avinash Karkada Ashok, et al.
Journal of Molecular Structure (2024) Vol. 1321, pp. 139963-139963
Closed Access
Fe3O4@BA-Imid-Pyrim-Pd(0) Nanocomposite: An Efficient and Recoverable Catalyst for Azidation/Carbonylation Coupling Reactions
Yi Zheng, Mostafa R. Abukhadra, Mehdi Tlija, et al.
Journal of Inorganic and Organometallic Polymers and Materials (2024)
Closed Access
Parsing p-tolyloxy-1,3,4-oxadiazolepropanamides as 15-lipoxygenase inhibitors prop up by in vitro and in silico profiling including structure determination
Bushra Bashir, Naheed Riaz, Syeda Abida Ejaz, et al.
Journal of Molecular Structure (2022) Vol. 1275, pp. 134664-134664
Closed Access | Times Cited: 3
Modular and Computational Access to Innocuous Multistep Metal-Free Synthesis of 1,3,4-Oxadiazoles as Enzyme Inhibitors
Muhammad Umair, Azizur Rehman, Muhammad Athar Abbasi, et al.
ACS Omega (2023) Vol. 8, Iss. 13, pp. 11952-11965
Open Access
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