Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Novel guanidine derivatives targeting leukemia as selective Src/Abl dual inhibitors: Design, synthesis and anti-proliferative activity
Amr H. Moustafa, Asmaa M. AboulMagd, Ali M. Ali, et al.
Bioorganic Chemistry (2024) Vol. 147, pp. 107410-107410
Closed Access | Times Cited: 11

Showing 11 citing articles:

Design, synthesis, antineoplastic activity of new pyrazolo[3,4-d]pyrimidine derivatives as dual CDK2/GSK3β kinase inhibitors; molecular docking study, and ADME prediction
Mohamed T. M. Nemr, Ahmed Elshewy, Mohammed L. Ibrahim, et al.
Bioorganic Chemistry (2024) Vol. 150, pp. 107566-107566
Closed Access | Times Cited: 10
Design, synthesis and cytotoxic evaluation of new thieno[2,3-d]pyrimidine analogues as VEGFR-2/AKT dual inhibitors, apoptosis and autophagy inducers
Heba K. Abd El-Mawgoud, Asmaa M. AboulMagd, Mohamed T. M. Nemr, et al.
Bioorganic Chemistry (2024) Vol. 150, pp. 107622-107622
Closed Access | Times Cited: 8
Synthesis of tetra-substituted thiophene derivatives as potential Hits combating antibiotic resistant bacteria ESKAPE
Heba K. Abd El-Mawgoud, Asmaa M. AboulMagd, Ahmed Shaker, et al.
Bioorganic Chemistry (2025) Vol. 155, pp. 108101-108101
Closed Access
Advancing Src Kinase Inhibition: From Structural Design to Therapeutic Innovation - A Comprehensive Review
Yifeng Su, Kun Zhu, Jiahao Wang, et al.
European Journal of Medicinal Chemistry (2025) Vol. 287, pp. 117369-117369
Closed Access
Nitrogen, Oxygen, and Sulphur Heterocycles as Potent Anti‐Inflammatory Agents: Insight Into the Synthetic Routes
Mariam Khadri, Uday Shashikumar, Pei‐Chien Tsai, et al.
ChemistrySelect (2025) Vol. 10, Iss. 9
Closed Access
Novel benzenesulfonamide derivatives as potential selective carbonic anhydrase IX, XII inhibitors with anti-proliferative activity: Design, synthesis and in silico studies
Wael A.A. Fadaly, Fatma El Zahraa Ammar Mohamed, Mohamed T. M. Nemr, et al.
Bioorganic Chemistry (2024) Vol. 153, pp. 107881-107881
Closed Access | Times Cited: 4
Design, synthesis and biological evaluation of thienopyridine derivatives as c-Met kinase inhibitors
Tianyu Xie, Wenbo Hu, Lin You, et al.
Molecular Diversity (2024)
Closed Access | Times Cited: 3
Structural activity of synthesized pyrimidine-thiophene and pyrimidine-thiadiazole conjugates as anticancer agents
Abeer Mogadem, Abrar Bayazeed, Abdulmajeed F. Alrefaei, et al.
Results in Chemistry (2024) Vol. 11, pp. 101813-101813
Open Access | Times Cited: 2
An overview on pharmaceutical applications of phosphodiesterase enzyme 5 (PDE5) inhibitors
Mohamed T. M. Nemr, Mohamad Abdelaziz, Mohamed Teleb, et al.
Molecular Diversity (2024)
Open Access | Times Cited: 1
Synthesis, biological activities and mechanistic studies of C20-ketone pachysandra alkaloids as anti-hepatocellular carcinoma agents
Jinfeng Zhao, Jing Bai, Xiang Yu, et al.
Molecular Diversity (2024)
Closed Access
New chalcone incorporated structurally modified pyridine‐pyrimidine derivatives as anticancer agents: Their design, synthesis, and in‐vitro evaluation
Swarupa Ketha, Chithaluri Sudhakar, Shashikala Kethireddy, et al.
Chemistry & Biodiversity (2024) Vol. 21, Iss. 12
Closed Access
Discovery and optimization of 4-(imidazo[1,2-a]pyrimidin-3-yl)thiazol-2-amine derivatives as novel phosphodiesterase 4 inhibitors
Zongmin Wu, Furong Zhang, Zhexin Chen, et al.
Molecular Diversity (2024)
Closed Access
Page 1

Scroll to top