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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:

Identification of pyrrolo[3′,4’:3,4]cyclohepta[1,2-d][1,2]oxazoles as promising new candidates for the treatment of lymphomas
Marilia Barreca, Virginia Spanò, Roberta Rocca, et al.
European Journal of Medicinal Chemistry (2023) Vol. 254, pp. 115372-115372
Open Access | Times Cited: 25

Showing 25 citing articles:

The Role of Five-Membered Heterocycles in the Molecular Structure of Antibacterial Drugs Used in Therapy
Aura Rusu, I. Moga, Livia Uncu, et al.
Pharmaceutics (2023) Vol. 15, Iss. 11, pp. 2554-2554
Open Access | Times Cited: 58
Novel 4-(2-arylidenehydrazineyl)thienopyrimidine derivatives as anticancer EGFR inhibitors: Design, synthesis, biological evaluation, kinome selectivity and in silico insights
Heba A. Elsebaie, Eman A. El-Bastawissy, Kamel M. Elberembally, et al.
Bioorganic Chemistry (2023) Vol. 140, pp. 106799-106799
Closed Access | Times Cited: 23
The Effect of 4-(Dimethylamino)phenyl-5-oxopyrrolidines on Breast and Pancreatic Cancer Cell Colony Formation, Migration, and Growth of Tumor Spheroids
Karolina Kairytė, Rita Vaickelionienė, Birutė Grybaitė, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 3, pp. 1834-1834
Open Access | Times Cited: 5
Design, Synthesis, Molecular Modeling, In Vitro and In Vivo Biological Evaluation of Potent Anthranilamide Derivatives as Dual P-glycoprotein and CYP3A4 Inhibitors
Ahmed M. Said, Yara E. Mansour, Radwa R. Soliman, et al.
European Journal of Medicinal Chemistry (2024) Vol. 273, pp. 116492-116492
Closed Access | Times Cited: 5
Targeting hematological malignancies with isoxazole derivatives
Monika Majirská, Martina Bago Pilátová, Z Kudlicková, et al.
Drug Discovery Today (2024) Vol. 29, Iss. 8, pp. 104059-104059
Open Access | Times Cited: 5
Discovery of novel 6-p-tolyl-3-(3,4,5-trimethoxybenzyl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine derivative as a potent tubulin inhibitor with promising in vivo antitumor activity
Tangyang Ji, Xie‐Er Jian, Lin Chen, et al.
European Journal of Medicinal Chemistry (2023) Vol. 256, pp. 115437-115437
Closed Access | Times Cited: 12
Natural Products–Pyrazine Hybrids: A Review of Developments in Medicinal Chemistry
Guoqing Chen, Hongyan Guo, Zhe‐Shan Quan, et al.
Molecules (2023) Vol. 28, Iss. 21, pp. 7440-7440
Open Access | Times Cited: 12
Anticancer potential and structure activity studies of purine and pyrimidine derivatives: an updated review
T. K. MANNA, Sumit Maji, M. Mondal A. Maity, et al.
Molecular Diversity (2024) Vol. 29, Iss. 1, pp. 817-848
Closed Access | Times Cited: 4
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
Novel 4-Aryl-4H-chromene derivative displayed excellent in vivo anti-glioblastoma efficacy as the microtubule-targeting agent
Haoyi Yang, Dongyu Zhang, Ziyang Yuan, et al.
European Journal of Medicinal Chemistry (2024) Vol. 267, pp. 116205-116205
Closed Access | Times Cited: 3
Structure-based design and synthesis of BML284 derivatives: A novel class of colchicine-site noncovalent tubulin degradation agents
Chufeng Zhang, Wei Yan, Yan Liu, et al.
European Journal of Medicinal Chemistry (2024) Vol. 268, pp. 116265-116265
Closed Access | Times Cited: 2
Discovery and biological evaluation of 6-aryl-4-(3,4,5-trimethoxyphenyl)quinoline derivatives with promising antitumor activities as novel colchicine-binding site inhibitors
Qianqian Xu, Yuxuan Tu, Yujing Zhang, et al.
European Journal of Medicinal Chemistry (2024) Vol. 279, pp. 116869-116869
Closed Access | Times Cited: 2
Benzimidazoles Containing Piperazine Skeleton at C-2 Position as Promising Tubulin Modulators with Anthelmintic and Antineoplastic Activity
Kameliya Anichina, Anelia Ts. Mavrova, Dimitar Vuchev, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 11, pp. 1518-1518
Open Access | Times Cited: 4
Synthesis of Pyrrolo[3,4-b]pyridin-5-ones via Ugi–Zhu Reaction and In Vitro–In Silico Studies against Breast Carcinoma
Ivette Morales-Salazar, Carlos E. Garduño-Albino, Flora P. Montes-Enríquez, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 11, pp. 1562-1562
Open Access | Times Cited: 4
Structure-based approaches for the design of 6-aryl-1-(3,4,5-trimethoxyphenyl)-1H-benzo[d][1,2,3]triazoles as tubulin polymerization inhibitors
Mingxin Huang, Hongyao Han, H.C. Liu, et al.
European Journal of Medicinal Chemistry (2024) Vol. 269, pp. 116309-116309
Closed Access | Times Cited: 1
Can O-GIcNAc Transferase (OGT) Complex Be Used as a Target for the Treatment of Hematological Malignancies?
Shiwei Zhuang, Zhimei Liu, Jinyao Wu, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 6, pp. 664-664
Open Access | Times Cited: 1
Identification of 3-Aryl-1-benzotriazole-1-yl-acrylonitrile as a Microtubule-Targeting Agent (MTA) in Solid Tumors
Stefano Zoroddu, Luca Sanna, Valentina Bordoni, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 11, pp. 5704-5704
Open Access | Times Cited: 1
Repurposing Study of 4-Acyl-1-phenylaminocarbonyl-2-substituted-piperazine Derivatives as Potential Anticancer Agents—In Vitro Evaluation against Breast Cancer Cells
Emilio Guillén-Mancina, María del Rosario García-Lozano, Estefanía Burgos‐Morón, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 17041-17041
Open Access | Times Cited: 2
Evaluation of Antitumor Activity of Xanthones Conjugated with Amino Acids
Flávia Barbosa, Joana Araújo, Virgínia M. F. Gonçalves, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2121-2121
Open Access
Design, Synthesis and Biological Evaluation of Novel Tubulin-Targeting Agents with a Dual-Mechanism for Polymerization Inhibition and Protein Degradation
Sibo Wang, Jiahao Wang, Xiankun Lu, et al.
(2024)
Closed Access
New strategies to hit hematological cancers
Marilia Barreca, Francesco Bertoni, Paola Barraja
European Journal of Medicinal Chemistry (2024) Vol. 270, pp. 116350-116350
Closed Access
Design, synthesis and biological evaluation of novel tubulin-targeting agents with a dual-mechanism for polymerization inhibition and protein degradation
Sibo Wang, Jiahao Wang, Xiankun Lu, et al.
European Journal of Medicinal Chemistry (2024) Vol. 272, pp. 116458-116458
Closed Access
Promising anti-proliferative indolic benzenesulfonamides alter mechanisms with sulfonamide nitrogen substituents
Raúl Fuentes-Martín, Pilar Ayuda-Durán, Robert Hanes, et al.
European Journal of Medicinal Chemistry (2024) Vol. 275, pp. 116617-116617
Open Access
Development of Novel Indole and Coumarin Derivatives as Antibacterial Agents That Target Histidine Kinase in S. aureus
Lisha K. Poonacha, Rashmi Ramesh, Akshay Ravish, et al.
Applied Microbiology (2023) Vol. 3, Iss. 4, pp. 1214-1228
Open Access | Times Cited: 1
Monofluoromethylation of N-Heterocyclic Compounds
Mikhail Yu. Moskalik
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 24, pp. 17593-17593
Open Access | Times Cited: 1
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