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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:

Recent contributions of quinolines to antimalarial and anticancer drug discovery research
Tim Van de Walle, Lore Cools, Sven Mangelinckx, et al.
European Journal of Medicinal Chemistry (2021) Vol. 226, pp. 113865-113865
Open Access | Times Cited: 52

Showing 1-25 of 52 citing articles:

Synthesis, crystal structure, DFT calculations, NBO, Fukui function, NCI-RDG, Hirshfeld surface analysis, NLO properties and molecular docking analysis on (E)-N'-(3-methoxybenzylidene)-2-(quinolin-8-yloxy) acetohydrazide
Amar Chebli, Ahmed Djafri, Nourdine Boukabcha, et al.
Journal of Molecular Structure (2024) Vol. 1310, pp. 138287-138287
Closed Access | Times Cited: 6
Synthesis, In Vitro, and In Silico Approach to Quinoline-Arylsulfonate Derivatives as Antimicrobial Agents: DFT, Molecular Docking, and ADMET Studies
Nikhat Manzoor, Afreen Inam, Sabahat Samreen, et al.
Synthesis (2025)
Closed Access
A facile, environmentally-benign, green and a novel synthesis of tert-butyl-quinolines by using Fe3O4-MWCNT@CeO2 as recyclable catalyst
Adapaka Venkateswara Rao, Suresh Maddila, Sai Sonali Anantha, et al.
Inorganic Chemistry Communications (2024) Vol. 162, pp. 112280-112280
Closed Access | Times Cited: 4
Six‐Membered Aromatic Nitrogen Heterocyclic Anti‐Tumor Agents: Synthesis and Applications
Jiatong Li, Ao Gu, Xiao‐Mei Nong, et al.
The Chemical Record (2023) Vol. 23, Iss. 12
Closed Access | Times Cited: 13
Discovery of novel quinoline scaffold selective estrogen receptor degraders (SERDs) for treatment of ER positive breast cancer with enhanced antiproliferative bioactivity through immunogenic cell death (ICD) effects
Yunlong Lu, Zhenlin Liang, Lijuan Liu, et al.
European Journal of Medicinal Chemistry (2024) Vol. 275, pp. 116534-116534
Closed Access | Times Cited: 3
Design, development, and solvatochromic investigation of AIEE responsive Schiff base formulated from 5-aminoquinoline: DFT assessment and application as dual detection probe for Co2+ and Mg2+ ions
Nittish Sharma, Navjot Sandhu
Journal of Photochemistry and Photobiology A Chemistry (2024) Vol. 457, pp. 115903-115903
Closed Access | Times Cited: 3
Ring opening ring closure reactions with 5,9-diethyl-7-(chromon-3-yl)-7-hydroquinolino[3′,4′:5,6]pyrano[3,2-c]quinoline-6,8(5H,9H)-dione with some 1,2-binucleophiles: Synthesis, characterization, DFT study and biological activity
Al‐Shimaa Badran, Aya Ahmed, Asmaa I. Nabeel, et al.
Journal of Molecular Structure (2023) Vol. 1298, pp. 137030-137030
Closed Access | Times Cited: 10
Antioxidant and Anticancer Potential of the New Cu(II) Complexes Bearing Imine-Phenolate Ligands with Pendant Amine N-Donor Groups
Adriana Castro Pinheiro, Ianka Jacondino Nunes, Wesley Vieira Ferreira, et al.
Pharmaceutics (2023) Vol. 15, Iss. 2, pp. 376-376
Open Access | Times Cited: 9
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
Design, Synthesis, and Anticancer and Antibacterial Activities of Quinoline-5-Sulfonamides
Andrzej Zięba, Dominika Pindjaková, Małgorzata Latocha, et al.
Molecules (2024) Vol. 29, Iss. 17, pp. 4044-4044
Open Access | Times Cited: 2
Quinoline Synthesis: Nanocatalyzed Green Protocols─An Overview
Rangappa S. Keri, Srinivasa Budagumpi, Vinayak Adimule
ACS Omega (2024) Vol. 9, Iss. 42, pp. 42630-42667
Open Access | Times Cited: 2
Schiff bases as linker in the development of quinoline-sulfonamide hybrids as selective cancer-associated carbonic anhydrase isoforms IX/XII inhibitors: A new regioisomerism tactic
Afaf El‐Malah, Ehab S. Taher, Andrea Angeli, et al.
Bioorganic Chemistry (2022) Vol. 131, pp. 106309-106309
Closed Access | Times Cited: 14
Deaminative Cyclization of Tertiary Amines for the Synthesis of 2-Arylquinoline Derivatives with a Nonsubstituted Vinylene Fragment
Qinghe Gao, Yimei Guo, Zhenhua Sun, et al.
Organic Letters (2022) Vol. 25, Iss. 1, pp. 109-114
Closed Access | Times Cited: 13
Design, synthesis, and biological evaluation of quinoline-piperazine/pyrrolidine derivatives as possible antileishmanial agents
Sarita Katiyar, Ramalingam Karthik Raja, Abhishek Kumar, et al.
European Journal of Medicinal Chemistry (2023) Vol. 261, pp. 115863-115863
Closed Access | Times Cited: 6
Uracil as a Zn-Binding Bioisostere of the Allergic Benzenesulfonamide in the Design of Quinoline–Uracil Hybrids as Anticancer Carbonic Anhydrase Inhibitors
Samar El‐Kalyoubi, Ehab S. Taher, Tarek S. Ibrahim, et al.
Pharmaceuticals (2022) Vol. 15, Iss. 5, pp. 494-494
Open Access | Times Cited: 11
Inverse Electron Demand Diels Alder Reaction of Aza-o-Quinone Methides and Enaminones: Accessing 3-Aroyl Quinolines and Indeno[1,2-b]quinolinones
P Rahul, S Veena, Jubi John
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 21, pp. 13708-13714
Closed Access | Times Cited: 10
A bench-stable reagent for C-4 selective deuteriodifluoromethylation of azines
Junqing Liang, Lefeng Dong, Feng Qian, et al.
Chinese Chemical Letters (2022) Vol. 33, Iss. 11, pp. 4817-4821
Closed Access | Times Cited: 9
The Anticancer Effect of a Novel Quinoline Derivative 91b1 through Downregulation of Lumican
Yuanyuan Zhou, Zhongguo Zhou, Dessy Chan, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 21, pp. 13181-13181
Open Access | Times Cited: 9
Construction of Chiral Cyclobutanone-Fused 4-Aminoquinolines via Sequential Chiral Phosphoric Acid and Palladium Catalysis
Si Zhang, Ruoshi Jin, Yanfei Niu, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 7, pp. 4627-4632
Closed Access | Times Cited: 5
Lewis acid-mediated modular route to the synthesis of 3-substituted quinolines from 2-aminobenzyl alcohols and enamine(one)s
Aritra Ghosh, Samridhi Upadhyay, Dipak J. Dahatonde, et al.
New Journal of Chemistry (2024) Vol. 48, Iss. 15, pp. 6902-6910
Closed Access | Times Cited: 1
Design, Synthesis, and In Vitro Antimalarial Evaluation of New 1,3,5-Tris[(4-(Substituted-Aminomethyl)Phenoxy)Methyl]Benzenes
Sandra Albenque-Rubio, Jean Guillon, Patrice Agnamey, et al.
Drugs and Drug Candidates (2024) Vol. 3, Iss. 3, pp. 615-637
Open Access | Times Cited: 1
Design, synthesis and molecular docking study of novel quinoline–triazole molecular hybrids as anticancer agents
Rajubai D. Bakale, Amruta N. Bhagat, Udhav V. Mhetre, et al.
Journal of Molecular Structure (2024), pp. 140072-140072
Closed Access | Times Cited: 1
Investigation of new 1,2,3-triazolyl-quinolinyl-propan-2-ol derivatives as potential antimicrobial agents: in vitro and in silico approach
Abhijit D. Shinde, Yogesh Nandurkar, Swapnil Bhalekar, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 3, pp. 1191-1207
Closed Access | Times Cited: 4
Hybrids of 1,4-Quinone with Quinoline Derivatives: Synthesis, Biological Activity, and Molecular Docking with DT-Diaphorase (NQO1)
Monika Kadela-Tomanek, Maria Jastrzębska, Elwira Chrobak, et al.
Molecules (2022) Vol. 27, Iss. 19, pp. 6206-6206
Open Access | Times Cited: 7
Design, Synthesis, and Antiprotozoal Evaluation of New Promising 2,9-Bis[(substituted-aminomethyl)]-4,7-phenyl-1,10-phenanthroline Derivatives, a Potential Alternative Scaffold to Drug Efflux
Jean Guillon, Anita Cohen, Clotilde Boudot, et al.
Pathogens (2022) Vol. 11, Iss. 11, pp. 1339-1339
Open Access | Times Cited: 7
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