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:

New antileishmanial quinoline linked isatin derivatives targeting DHFR-TS and PTR1: Design, synthesis, and molecular modeling studies
Ahmed Sabt, Wagdy M. Eldehna, Tamer M. Ibrahim, et al.
European Journal of Medicinal Chemistry (2022) Vol. 246, pp. 114959-114959
Closed Access | Times Cited: 21

Showing 21 citing articles:

Discovery of sulfonamide-tethered isatin derivatives as novel anticancer agents and VEGFR-2 inhibitors
Moataz A. Shaldam, Hadia Almahli, Andrea Angeli, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 26

Identification of new anti-mycobacterial agents based on quinoline-isatin hybrids targeting enoyl acyl carrier protein reductase (InhA)
Eman F. Khaleel, Ahmed Sabt, Małgorzata Korycka-Machała, et al.
Bioorganic Chemistry (2024) Vol. 144, pp. 107138-107138
Closed Access | Times Cited: 8

Identification of sulphonamide-tethered N -((triazol-4-yl)methyl)isatin derivatives as inhibitors of SARS-CoV-2 main protease
Mai H. ElNaggar, Abdullah A. Elgazar, Ghada Gamal, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 13

1-Benzyl-5-bromo-3-hydrazonoindolin-2-ones as Novel Anticancer Agents: Synthesis, Biological Evaluation and Molecular Modeling Insights
Tarfah Al‐Warhi, Hadia Almahli, Raed M. Maklad, et al.
Molecules (2023) Vol. 28, Iss. 7, pp. 3203-3203
Open Access | Times Cited: 11

Isatin-based ibuprofen and mefenamic acid Schiff base derivatives as dual inhibitors against urease and α–glucosidase: In vitro, in silico and cytotoxicity studies
Saima Daud, Obaid‐ur‐Rahman Abid, Malik Saadullah, et al.
Journal of Saudi Chemical Society (2024) Vol. 28, Iss. 5, pp. 101905-101905
Open Access | Times Cited: 2

Discovery of new quinoline derivatives bearing 1-aryl-1,2,3-triazole motif as influenza H1N1 virus neuraminidase inhibitors
Ahmed Sabt, Eman F. Khaleel, Moataz A. Shaldam, et al.
Bioorganic Chemistry (2024) Vol. 151, pp. 107703-107703
Closed Access | Times Cited: 2

Identification of 2-(N-aryl-1,2,3-triazol-4-yl) quinoline derivatives as antitubercular agents endowed with InhA inhibitory activity
Ahmed Sabt, Maha-Hamadien Abdulla, Manal S. Ebaid, et al.
Frontiers in Chemistry (2024) Vol. 12
Open Access | Times Cited: 2

A Review on Synthesis and Biological Applications of Quinoline Derivative as Fused Aromatic Compounds
Md. Mohasin, Md. Zafer Alam, Qasim Ullah, et al.
Polycyclic aromatic compounds (2023), pp. 1-30
Closed Access | Times Cited: 7

Kaurane-Type Diterpenoids as Potential Inhibitors of Dihydrofolate Reductase-Thymidylate Synthase in New World Leishmania Species
Chonny Herrera‐Acevedo, Renata Priscila Barros de Menezes, Natália Ferreira de Sousa, et al.
Antibiotics (2023) Vol. 12, Iss. 4, pp. 663-663
Open Access | Times Cited: 6

Sojourn of Nitrogenous Heterocycles as Promising Antileishmanial Agents: Medicinal Perspectives and Structure–Activity Relationship Studies
Bhupender Nehra, Manoj Kumar, Sumitra Singh, et al.
Chemistry Africa (2024) Vol. 7, Iss. 7, pp. 3485-3529
Closed Access | Times Cited: 1

Hit-to-lead optimization of 4,5-dihydrofuran-3-sulfonyl scaffold against Leishmania amazonensis. Effect of an aliphatic moiety.
O. León, Fabiana Maia Santos Urbancg Moncorvo, Christophe Curti, et al.
European Journal of Medicinal Chemistry (2024) Vol. 280, pp. 116935-116935
Open Access | Times Cited: 1

Design and synthesis of N-acyl and dimeric N-Arylpiperazine derivatives as potential antileishmanial agents
Shabina B. Ansari, Sakshi Kamboj, Ramalingam Karthik Raja, et al.
Bioorganic Chemistry (2023) Vol. 137, pp. 106593-106593
Closed Access | Times Cited: 3

Isatin Derivatives: A Frontier in Antimicrobial Agents
Shareef Shaik, Manish Chaudhary, Charanjit Kaur, et al.
Letters in Organic Chemistry (2023) Vol. 21, Iss. 4, pp. 333-350
Closed Access | Times Cited: 3

Antibacterial Activity of Quinoline‐Based Derivatives against Methicillin‐Resistant Staphylococcus aureus and Pseudomonas aeruginosa: Design, Synthesis, DFT and Molecular Dynamic Simulations
Ahmed Sabt, Mohamed Abdelraof, Mohamed Farouk Hamissa, et al.
Chemistry & Biodiversity (2023) Vol. 20, Iss. 11
Closed Access | Times Cited: 3

Antileishmanial natural products as potential inhibitors of the Leishmania pteridine reductase: insights from molecular docking and molecular dynamics simulations
Abigail Kusiwaa Adomako, Edward Ntim Gasu, Jehoshaphat Oppong Mensah, et al.
In Silico Pharmacology (2024) Vol. 12, Iss. 2
Closed Access

Spiro-fused indoline-quinazoline hybrids as smart bombs against TNF-α-mediated inflammation
Mahmoud S. Elkotamy, Mohamed K. Elgohary, Mahmoud Abdelrahman Alkabbani, et al.
International Journal of Biological Macromolecules (2024) Vol. 283, pp. 137554-137554
Closed Access

Antileishmanial potential of thiourea-based derivatives: design, synthesis and biological activity
Abdul Hadi Abd Rahman, Muhammad Yaqoob, Fahad Hussain, et al.
RSC Advances (2024) Vol. 14, Iss. 50, pp. 37131-37141
Open Access

Machine Learning and Structure-based Virtual Screening for Selecting Cinnamic Acid Derivatives as Leishmania major DHFR-TS Inhibitors
Maria Camila Muñoz-Vega, Sofía López-Hernández, Adrián Sierra-Chavarro, et al.
(2023)
Open Access | Times Cited: 1

Machine-Learning- and Structure-Based Virtual Screening for Selecting Cinnamic Acid Derivatives as Leishmania major DHFR-TS Inhibitors
Maria Camila Muñoz-Vega, Sofía López-Hernández, Adrián Sierra-Chavarro, et al.
Molecules (2023) Vol. 29, Iss. 1, pp. 179-179
Open Access

Structure-Based Design and Virtual Screening of Indole Scaffolds Targeting Plasmodium falciparum: An Experimental and Computational Approach for Antimalarial Drug Discovery
Anurag Shama, Mallika Savaliya, Nutan Prakash Vishwakarma
Russian Journal of General Chemistry (2023) Vol. 93, Iss. S4, pp. S993-S1005
Closed Access

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