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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:

Discovery of (2-(pyrrolidin-1-yl)thieno[3,2-d]pyrimidin-4-yl)(3,4,5-trimethoxyphenyl)methanone as a novel potent tubulin depolymerizing and vascular disrupting agent
Chao Tian, Meng Wang, Xueqi Shi, et al.
European Journal of Medicinal Chemistry (2022) Vol. 238, pp. 114466-114466
Closed Access | Times Cited: 9

Showing 9 citing articles:

Discovery of novel N-benzylarylamide-dithiocarbamate based derivatives as dual inhibitors of tubulin polymerization and LSD1 that inhibit gastric cancers
Xin-Ying Yuan, Chun-Hong Song, Xiujuan Liu, et al.
European Journal of Medicinal Chemistry (2023) Vol. 252, pp. 115281-115281
Closed Access | Times Cited: 17
Discovery of novel thienopyridine indole derivatives as inhibitors of tubulin polymerization targeting the colchicine-binding site with potent anticancer activities
Wen‐Bo Liu, Weiguang Yang, Ji Wu, et al.
European Journal of Medicinal Chemistry (2025) Vol. 286, pp. 117314-117314
Closed Access
Discovery of a novel Coumarin-Dihydroquinoxalone derivative MY-673 as a tubulin polymerization inhibitor capable of inhibiting the ERK pathway with potent anti-gastric cancer activities
Jian Song, Shuyu Wang, Xiao Wang, et al.
Bioorganic Chemistry (2023) Vol. 137, pp. 106580-106580
Closed Access | Times Cited: 8
Design and Synthesis of New 4-(3,4,5-Trimethoxyphenyl)Thiazole–Pyrimidine Derivatives as Potential Antiproliferative Agents
Ashraf K. El‐Damasy, Heewon Jin, Mohamed Sabry, et al.
Medicina (2023) Vol. 59, Iss. 6, pp. 1076-1076
Open Access | Times Cited: 5
Design, synthesis and biological evaluation of N-benzylaryl cinnamide derivatives as tubulin polymerization inhibitors capable of promoting YAP degradation with potent anti-gastric cancer activities
Xiang-Jing Fu, Jiao Huang, Na Li, et al.
European Journal of Medicinal Chemistry (2023) Vol. 262, pp. 115883-115883
Closed Access | Times Cited: 5
Design, synthesis, and bioevaluation of imidazo [1,2–a] pyrazine derivatives as tubulin polymerization inhibitors with potent anticancer activities
Bulian Deng, Zhiqiang Sun, Yuxi Wang, et al.
Bioorganic & Medicinal Chemistry (2022) Vol. 76, pp. 117098-117098
Closed Access | Times Cited: 6
S-72, a Novel Orally Available Tubulin Inhibitor, Overcomes Paclitaxel Resistance via Inactivation of the STING Pathway in Breast Cancer
Zhenyan Hou, Songwen Lin, Tingting Du, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 5, pp. 749-749
Open Access | Times Cited: 2
Design, synthesis, and biological evaluation of new biaryl derivatives of cycloalkyl diacetamide bearing chalcone moiety as type II c-MET kinase inhibitors
Somayeh Salarinejad, Soheila Seyfi, Seiko Hayashi, et al.
Molecular Diversity (2024)
Open Access
Design, Synthesis, and Biological Evaluation of New Biaryl Derivatives of Cycloalkyl diacetamide Bearing Chalcone Moiety as type II c-MET Kinase Inhibitors
Somayeh Salarinejad, Soheila Seyfi, Seiko Hayashi, et al.
Research Square (Research Square) (2023)
Open Access
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