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:
Phenoxytacrine derivatives: Low-toxicity neuroprotectants exerting affinity to ifenprodil-binding site and cholinesterase inhibition
Anna Misiachna, Barbora Svobodová, Jakub Netolický, et al.
European Journal of Medicinal Chemistry (2024) Vol. 266, pp. 116130-116130
Open Access | Times Cited: 8
Anna Misiachna, Barbora Svobodová, Jakub Netolický, et al.
European Journal of Medicinal Chemistry (2024) Vol. 266, pp. 116130-116130
Open Access | Times Cited: 8
Showing 8 citing articles:
Prophylaxis by a reversible cholinesterase inhibitor and the treatment NMDA receptor antagonists as combinatorial countermeasure against nerve agent poisoning in mice model
Jiřı́ Kassa, Jan Konečný, Barbora Svobodová, et al.
Chemico-Biological Interactions (2025) Vol. 407, pp. 111386-111386
Closed Access
Jiřı́ Kassa, Jan Konečný, Barbora Svobodová, et al.
Chemico-Biological Interactions (2025) Vol. 407, pp. 111386-111386
Closed Access
Investigation of small molecules disrupting dengue virus assembly by inhibiting capsid protein and blocking RNA encapsulation
Hrithika Panday, Abhimanyu Kumar Jha, Vivek Dhar Dwivedi
Molecular Diversity (2024)
Closed Access | Times Cited: 1
Hrithika Panday, Abhimanyu Kumar Jha, Vivek Dhar Dwivedi
Molecular Diversity (2024)
Closed Access | Times Cited: 1
Annulated and spiro-molecular systems from cycloheptane-based β-ketoesters: Synthesis, reactivity, and biological applications
Sherif M. H. Sanad, Ahmed E. M. Mekky, Rahma M.B. Hussein, et al.
Journal of Molecular Structure (2024), pp. 141274-141274
Closed Access | Times Cited: 1
Sherif M. H. Sanad, Ahmed E. M. Mekky, Rahma M.B. Hussein, et al.
Journal of Molecular Structure (2024), pp. 141274-141274
Closed Access | Times Cited: 1
Three new antinociceptive diterpenoids from the fruits of Rhododendron molle
Ying-Ying Zhu, Yang‐Lan Liu, Bing Chai, et al.
Journal of Asian Natural Products Research (2024) Vol. 26, Iss. 9, pp. 1024-1032
Closed Access
Ying-Ying Zhu, Yang‐Lan Liu, Bing Chai, et al.
Journal of Asian Natural Products Research (2024) Vol. 26, Iss. 9, pp. 1024-1032
Closed Access
Dizocilpine derivatives with neuroprotective effect lacking the psychomimetic side effects
Jan Konečný, Anna Misiachna, Markéta Chvojková, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Jan Konečný, Anna Misiachna, Markéta Chvojková, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Dizocilpine derivatives as neuroprotective NMDA receptor antagonists without psychomimetic side effects
Jan Konečný, Anna Misiachna, Markéta Chvojková, et al.
European Journal of Medicinal Chemistry (2024) Vol. 280, pp. 116981-116981
Open Access
Jan Konečný, Anna Misiachna, Markéta Chvojková, et al.
European Journal of Medicinal Chemistry (2024) Vol. 280, pp. 116981-116981
Open Access
Benzylpiperidine derivatives as new dual μ-opioid and σ1 receptor ligands with potent antinociceptive effects
Zong-Zheng Li, Zhen Wang, Chen Xiong, et al.
Bioorganic Chemistry (2024) Vol. 153, pp. 107921-107921
Closed Access
Zong-Zheng Li, Zhen Wang, Chen Xiong, et al.
Bioorganic Chemistry (2024) Vol. 153, pp. 107921-107921
Closed Access
The Effect of Tacrine on Functional Response of the Lower Oesophageal Sphincter Assessed by Endoscopic Luminal Impedance Planimetry in Experimental Pigs
Jan Bureš, Martin Novák, Věra Radochová, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 12, pp. 1588-1588
Open Access
Jan Bureš, Martin Novák, Věra Radochová, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 12, pp. 1588-1588
Open Access
