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:

Quinoline anticancer agents active on DNA and DNA-interacting proteins: From classical to emerging therapeutic targets
Antonino Lauria, Gabriele La Monica, Alessia Bono, et al.
European Journal of Medicinal Chemistry (2021) Vol. 220, pp. 113555-113555
Closed Access | Times Cited: 61

Showing 1-25 of 61 citing articles:

A review on metal complexes and its anti-cancer activities: Recent updates from in vivo studies
Suman Adhikari, Priyatosh Nath, Alakesh Das, et al.
Biomedicine & Pharmacotherapy (2024) Vol. 171, pp. 116211-116211
Open Access | Times Cited: 49

Quinoline–imidazole/benzimidazole derivatives as dual-/multi-targeting hybrids inhibitors with anticancer and antimicrobial activity
Dumitrela Diaconu, Vasilichia Antoci, Violeta Mangalagiu, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 37

Dynamic Kinetic Resolution of 2‐(Quinolin‐8‐yl)Benzaldehydes: Atroposelective Iridium‐Catalyzed Transfer Hydrogenative Allylation
José A. Carmona, Patricia Rodríguez‐Salamanca, Rosario Fernández, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 35
Open Access | Times Cited: 21

A new Fe(III) complex of quinoline-substituted β-enaminone: Magnetic properties in solutions and molecular docking
Alsu R. Sharipova, Ekaterina E. Batueva, А.Т. Губайдуллин, et al.
Inorganica Chimica Acta (2025), pp. 122547-122547
Closed Access

Design, synthesis, biological evaluation, and SAR studies of novel cyclopentaquinoline derivatives as DNA intercalators, topoisomerase II inhibitors, and apoptotic inducers
Mohamed M. Hammoud, Alaa S. Nageeb, M.A. Morsi, et al.
New Journal of Chemistry (2022) Vol. 46, Iss. 23, pp. 11422-11436
Closed Access | Times Cited: 33

Bioisosteric heterocyclic analogues of natural bioactive flavonoids by scaffold-hopping approaches: State-of-the-art and perspectives in medicinal chemistry
Gabriele La Monica, Alessia Bono, Federica Alamia, et al.
Bioorganic & Medicinal Chemistry (2024) Vol. 109, pp. 117791-117791
Open Access | Times Cited: 5

A Brief Review on the Synthesis of 4H‐Chromene‐Embedded Heterocycles
K. Nissi Sharon, P. Padmaja, Pedavenkatagari Narayana Reddy
ChemistrySelect (2024) Vol. 9, Iss. 27
Closed Access | Times Cited: 5

Copper(ii) complex enhanced chemodynamic therapy through GSH depletion and autophagy flow blockade
Wen-Ying Shen, Chun-Peng Jia, Li-Yi Liao, et al.
Dalton Transactions (2023) Vol. 52, Iss. 11, pp. 3287-3294
Closed Access | Times Cited: 12

Atroposelective Synthesis of 2‐(Quinolin‐8‐yl)benzyl Alcohols by Biocatalytic Dynamic Kinetic Resolutions
Juan M. Coto‐Cid, Gonzalo de Gonzalo, José A. Carmona, et al.
Advanced Synthesis & Catalysis (2023) Vol. 366, Iss. 4, pp. 909-915
Open Access | Times Cited: 10

Design and synthesis of new quinoline derivatives as selective C-RAF kinase inhibitors with potent anticancer activity
Seyed–Omar Zaraei, Nour N. Alach, Hanan S. Anbar, et al.
European Journal of Medicinal Chemistry (2022) Vol. 238, pp. 114434-114434
Open Access | Times Cited: 16

Acridine Based N-Acylhydrazone Derivatives as Potential Anticancer Agents: Synthesis, Characterization and ctDNA/HSA Spectroscopic Binding Properties
Mária Vilková, Monika Hudáčová, Nikola Palušeková, et al.
Molecules (2022) Vol. 27, Iss. 9, pp. 2883-2883
Open Access | Times Cited: 16

Recent advances in 3-aminoindazoles as versatile synthons for the synthesis of nitrogen heterocycles
Yimei Guo, Qinghe Gao
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 36, pp. 7138-7150
Closed Access | Times Cited: 16

A Small Sugar Molecule with Huge Potential in Targeted Cancer Therapy
Gabriela Pastuch-Gawołek, Julia Szreder, Monika Domińska, et al.
Pharmaceutics (2023) Vol. 15, Iss. 3, pp. 913-913
Open Access | Times Cited: 8

Rational Design of a Highly Sensitive Carboxylesterase Probe and Its Application in High-Throughput Screening for Uncovering Carboxylesterase Inhibitors
Kexin Wang, Ruoxi Wang, Zihui Yan, et al.
The Journal of Organic Chemistry (2024) Vol. 89, Iss. 20, pp. 14650-14657
Closed Access | Times Cited: 2

Synthesis of Ethyl Pyrimidine-Quinolincarboxylates Selected from Virtual Screening as Enhanced Lactate Dehydrogenase (LDH) Inhibitors
Iván Díaz, Sofı́a Salido, Manuel Nogueras, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9744-9744
Open Access | Times Cited: 2

Dynamic Kinetic Resolution of 2‐(Quinolin‐8‐yl)Benzaldehydes: Atroposelective Iridium‐Catalyzed Transfer Hydrogenative Allylation
José A. Carmona, Patricia Rodríguez‐Salamanca, Rosario Fernández, et al.
Angewandte Chemie (2023) Vol. 135, Iss. 35
Open Access | Times Cited: 7

Click Synthesis, Anticancer Activity, and Molecular Docking Investigation of some Functional 1,2,3-triazole Derivatives
Meryem Hrimla, Ali Oubella, Yassine Laamari, et al.
Biointerface Research in Applied Chemistry (2021) Vol. 12, Iss. 6, pp. 7633-7667
Open Access | Times Cited: 16

Design and synthesis of spiro[pyrrolidine-3,3'-quinoline]-2,2'-dione derivatives as novel antifungal agents targeting chitin synthase
Yan Long, Xinglong Yang, Yajie Xu, et al.
European Journal of Medicinal Chemistry (2024) Vol. 279, pp. 116895-116895
Closed Access | Times Cited: 1

Glycoconjugation of Quinoline Derivatives Using the C-6 Position in Sugars as a Strategy for Improving the Selectivity and Cytotoxicity of Functionalized Compounds
Monika Domińska, Gabriela Pastuch-Gawołek, Magdalena Skonieczna, et al.
Molecules (2022) Vol. 27, Iss. 20, pp. 6918-6918
Open Access | Times Cited: 9

Design and synthesis of novel 7-ethyl-10-fluoro-20-O-(cinnamic acid ester)-camptothecin derivatives as potential high selectivity and low toxicity topoisomerase I inhibitors for hepatocellular carcinoma
Yin-Peng Bai, Cheng‐Jie Yang, Nan Deng, et al.
Biochemical Pharmacology (2022) Vol. 200, pp. 115049-115049
Closed Access | Times Cited: 8

Copper(II) complexes with 3,5–dihalogeno–salicylaldehydes: Synthesis, structure and interaction with DNA and albumins
Aphrodite Christidou, Konstantina Zavalani, Antonios G. Hatzidimitriou, et al.
Journal of Inorganic Biochemistry (2022) Vol. 238, pp. 112049-112049
Closed Access | Times Cited: 8

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