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:

Molecular target interactions of quinoline derivatives as anticancer agents: A review
Vikas Pradhan, Salahuddin Salahuddin, Rajnish Kumar, et al.
Chemical Biology & Drug Design (2022) Vol. 101, Iss. 4, pp. 977-997
Closed Access | Times Cited: 10

Showing 10 citing articles:

An insight into sustainable and green chemistry approaches for the synthesis of quinoline derivatives as anticancer agents
B. Kumaraswamy, K. Hemalatha, Rohit Pal, et al.
European Journal of Medicinal Chemistry (2024) Vol. 275, pp. 116561-116561
Closed Access | Times Cited: 7

Hydroxamic acid hybrids: Histone deacetylase inhibitors with anticancer therapeutic potency
Yuan Jiang Pan, Haodong Hou, Bo Zhou, et al.
European Journal of Medicinal Chemistry (2023) Vol. 262, pp. 115879-115879
Closed Access | Times Cited: 6

Novel Quinolin-4-ylcarbonylhydrazine Having N-(3-Arylacryloyl) Moiety: Design, Synthesis and Biological Evaluation as Potential Cytotoxic Agents against MDA-MB-231 via Tubulin Assembly Inhibition
Hany M. Abd El‐Lateef, Tahani H. Alharbi, Eman Fayad, et al.
Journal of Molecular Structure (2024) Vol. 1321, pp. 140214-140214
Closed Access | Times Cited: 1

Increased Free Radical Generation during the Interaction of a Quinone-Quinoline Chelator with Metal Ions and the Enhancing Effect of Light
Olga Yu. Selyutina, Simon V. Babenko, Irina A. Slepneva, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 8, pp. 1116-1116
Open Access | Times Cited: 3

Insight into the Various Approaches Undertaken for the Synthesis of Quinoline Hybrids Imparting Diverse Therapeutic Activities
Ruchi Sharma, Chandana Majee, Rupa Mazumder, et al.
Letters in Organic Chemistry (2024) Vol. 21, Iss. 9, pp. 756-783
Closed Access

Current Scenario of Pyridine/Quinoline-Sulfonamide Hybrids with Anticancer Potential (A Review)
Guangbin Dong, Yu Feng, Jeh‐Jeng Wang, et al.
Russian Journal of General Chemistry (2024) Vol. 94, Iss. 4, pp. 989-1005
Closed Access

Tris{2-[N-(quinolin-8-yl)carbamoylmethoxy]phenyl}phosphine oxide: synthesis and coordination properties
Т. В. Баулина, I. Yu. Kudryavtsev, Маргарита П. Пасечник, et al.
Russian Chemical Bulletin (2024) Vol. 73, Iss. 10, pp. 3032-3037
Closed Access

Virtual Screening of Quinoline Antitumor Small Molecular Compounds Targeting the p53-MDM2 Interaction
涵静 丁
Pharmacy Information (2023) Vol. 12, Iss. 05, pp. 434-442
Closed Access

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