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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 Chalcone Derivatives as Inhibitors of Leishmania infantum Arginase and Promising Antileishmanial Agents
Andreza R. Garcia, Danielle Maria Perpétua de Oliveira, Jéssica B. de Jesus, et al.
Frontiers in Chemistry (2021) Vol. 8
Open Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

Synthetic product-based approach toward potential antileishmanial drug development
Rohit Pal, Ghanshyam Teli, Md Jawaid Akhtar, et al.
European Journal of Medicinal Chemistry (2023) Vol. 263, pp. 115927-115927
Closed Access | Times Cited: 16
The role of natural anti-parasitic guided development of synthetic drugs for leishmaniasis
Rohit Pal, Ghanshyam Teli, Md Jawaid Akhtar, et al.
European Journal of Medicinal Chemistry (2023) Vol. 258, pp. 115609-115609
Closed Access | Times Cited: 15
Antiviral and antimicrobial applications of chalcones and their derivatives: From nature to greener synthesis
Mohammad Hadi Nematollahi, Mehrnaz Mehrabani, Yaser Hozhabri, et al.
Heliyon (2023) Vol. 9, Iss. 10, pp. e20428-e20428
Open Access | Times Cited: 15
Red-shifted optical absorption induced by donor–acceptor–donor π-extended dibenzalacetone derivatives
Vitória M. R. Vasconcelos, Bruna Bueno Postacchini, Hélcio Silva dos Santos, et al.
RSC Advances (2025) Vol. 15, Iss. 4, pp. 2416-2429
Open Access
Evolution of Acridines and Xanthenes as a Core Structure for the Development of Antileishmanial Agents
Carlos F. M. Silva, Diana C. G. A. Pinto, Pedro Alexandrino Fernandes, et al.
Pharmaceuticals (2022) Vol. 15, Iss. 2, pp. 148-148
Open Access | Times Cited: 22
Evolution of the Quinoline Scaffold for the Treatment of Leishmaniasis: A Structural Perspective
Carlos F. M. Silva, Diana C. G. A. Pinto, Pedro Alexandrino Fernandes, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 3, pp. 285-285
Open Access | Times Cited: 4
Total Synthesis of the Natural Chalcone Lophirone E, Synthetic Studies toward Benzofuran and Indole-Based Analogues, and Investigation of Anti-Leishmanial Activity
Luca Pozzetti, Roberta Ibba, Sara Rossi, et al.
Molecules (2022) Vol. 27, Iss. 2, pp. 463-463
Open Access | Times Cited: 19
Antimicrobial, Antiproliferative Effects and Docking Studies of Methoxy Group Enriched Coumarin‐Chalcone Hybrids
Ahmad Badreddin Musatat, İlker Kılıçcıoğlu, Yener Kurman, et al.
Chemistry & Biodiversity (2023) Vol. 20, Iss. 3
Closed Access | Times Cited: 11
Synthesis, enzyme inhibition, and molecular docking studies of a novel chalcone series bearing benzothiazole scaffold
Ahmad Badreddin Musatat, Alparslan Atahan, Adem Ergün, et al.
Biotechnology and Applied Biochemistry (2023) Vol. 70, Iss. 3, pp. 1357-1370
Closed Access | Times Cited: 10
Metalloenzyme Inhibitors against Zoonotic Infections: Focus on Leishmania and Schistosoma
Sara Rossi, Valeria Tudino, Gabriele Carullo, et al.
ACS Infectious Diseases (2024) Vol. 10, Iss. 5, pp. 1520-1535
Closed Access | Times Cited: 3
Antileishmanial activity of 2-amino-thiophene derivative SB-200
João Paulo Araújo de Sousa, Julyanne Maria Saraiva de Sousa, Raiza Raianne Luz Rodrigues, et al.
International Immunopharmacology (2023) Vol. 123, pp. 110750-110750
Closed Access | Times Cited: 9
Identification of some chalcone analogues as potential antileishmanial agents: An integrated in vitro and in silico evaluation
Marwa Osman, Talal Ahmed Awad, Shaza W. Shantier, et al.
Arabian Journal of Chemistry (2022) Vol. 15, Iss. 4, pp. 103717-103717
Open Access | Times Cited: 15
Molecular-level strategic goals and repressors in Leishmaniasis – Integrated data to accelerate target-based heterocyclic scaffolds
M. Abirami, Banoth Karan Kumar, Faheem Faheem, et al.
European Journal of Medicinal Chemistry (2023) Vol. 257, pp. 115471-115471
Open Access | Times Cited: 8
A colorimetric assay adapted to fragment screening revealing aurones and chalcones as new arginase inhibitors
Jason Muller, Luca Marchisio, Rym Attia, et al.
RSC Medicinal Chemistry (2024) Vol. 15, Iss. 5, pp. 1722-1730
Closed Access | Times Cited: 2
Synthesis, Vibrational Analysis, Thermal analysis, Quantum-chemical Calculation, Molecular Docking and Dynamics, DMPK and Evaluation of the Antichagasic Potential of a Fluorinated Chalcone
João Victor Serra Nunes, Emanuelle Machado Marinho, Caio Henrique Alexandre Roberto, et al.
Journal of Molecular Structure (2024) Vol. 1318, pp. 139124-139124
Closed Access | Times Cited: 2
Computational screening of natural MtbDXR inhibitors for novel anti-tuberculosis compound discovery
Sabrina Islam, Rahagir Salekeen, Ayesha Ashraf
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 7, pp. 3593-3603
Closed Access | Times Cited: 7
Compounds with potentialities as novel chemotherapeutic agents in leishmaniasis at preclinical level
Maikel González-Matos, Mirtha Elisa Aguado, Maikel Izquierdo, et al.
Experimental Parasitology (2024) Vol. 260, pp. 108747-108747
Closed Access | Times Cited: 1
Transition Metal‐Catalyzed Transformations of Chalcones
Clementina M.M. Santos, Artur M. S. Silva
The Chemical Record (2024) Vol. 24, Iss. 8
Closed Access | Times Cited: 1
The Natural Alkaloid Tryptanthrin Induces Apoptosis-like Death in Leishmania spp.
Andreza R. Garcia, Yasmin P. G. Silva-Luiz, Celuta S. Alviano, et al.
Tropical Medicine and Infectious Disease (2022) Vol. 7, Iss. 6, pp. 112-112
Open Access | Times Cited: 6
Antileishmanial activities of three chalcone derivatives and their association with plasma membrane rigidity as assessed by EPR spectroscopy
E. Borges, Laís Alonso, Murilo Barros Silveira, et al.
Journal of Molecular Structure (2023) Vol. 1292, pp. 136123-136123
Closed Access | Times Cited: 3
Benzimidazole Derivatives as New and Selective Inhibitors of Arginase from Leishmania mexicana with Biological Activity against Promastigotes and Amastigotes
Irene Betancourt-Conde, Claudia Avitia‐Domínguez, Alicia Hernández–Campos, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 24, pp. 13613-13613
Open Access | Times Cited: 7
4-oxoquinoline-3-carboxamide acyclonucleoside phosphonates hybrids: Human MCF-7 breast cancer cell death induction by oxidative stress-promoting and in silico ADMET studies
Thayná Rocco Machado, Letícia V. Faro, Angélica Lauria do Nascimento Mello, et al.
Journal of Molecular Structure (2022) Vol. 1276, pp. 134542-134542
Closed Access | Times Cited: 5
Molecular Targets for Chalcones in Antileishmanial Drug Discovery
Kaio Maciel de Santiago-Silva, Gabriel Felix da Silva Gomes, Carla Cristina Perez, et al.
Mini-Reviews in Medicinal Chemistry (2023) Vol. 23, Iss. 14, pp. 1414-1434
Closed Access | Times Cited: 2
Structure‐based design of new N‐benzyl‐piperidine derivatives as multitarget‐directed AChE/BuChE inhibitors for Alzheimer's disease
Raissa Alves da Conceição, Natalia Lidmar von Ranke, Luciana Abrantes Pontes de Azevedo, et al.
Journal of Cellular Biochemistry (2023) Vol. 124, Iss. 11, pp. 1734-1748
Open Access | Times Cited: 2
Importance of R-CH3⋯O tetrel bonding and vinyl⋯aryl stacking interactions in stabilizing the crystal packing of 2’,4’-dihydroxy-3’-methoxychalcone: Exploration of antileishmanial activity and molecular docking studies
Eliana Rita Solórzano, Paolo Pastore, Alessandro Dolmella, et al.
Journal of Molecular Structure (2022) Vol. 1265, pp. 133357-133357
Closed Access | Times Cited: 4
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