Kaïss Aouadi
About
Kaïss Aouadi is a scholar working on Organic Chemistry, Molecular Biology and Food Science.
According to data from OpenAlex, Kaïss Aouadi has authored 81 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Organic Chemistry, 29 papers in Molecular Biology and 13 papers in Food Science. Recurrent topics in Kaïss Aouadi's work include Synthesis and biological activity (19 papers), Essential Oils and Antimicrobial Activity (13 papers) and Carbohydrate Chemistry and Synthesis (11 papers). Kaïss Aouadi is often cited by papers focused on Synthesis and biological activity (19 papers), Essential Oils and Antimicrobial Activity (13 papers) and Carbohydrate Chemistry and Synthesis (11 papers). Kaïss Aouadi collaborates with scholars based in Tunisia, Saudi Arabia and France. Kaïss Aouadi's co-authors include Adel Kadri, Mejdi Snoussi, Siwar Ghannay, Moncef Msaddek, Mohamed A. M. Gad‐Elkareem, Ismail M. M. Othman, Jean‐Pierre Praly, Emira Noumi, Sana Bakari and Mohd Adnan and has published in prestigious journals such as Angewandte Chemie International Edition, International Journal of Molecular Sciences and Tetrahedron.
In The Last Decade
Kaïss Aouadi
80 papers receiving 1.6k citations
Peers
Kaïss Aouadi
Avijit Mazumder India
Vesna Rastija Croatia
Ricardo José Nunes Brazil
Dhirender Kaushik India
Fyaz M.D. Ismail United Kingdom
Sudhir Kumar Paidesetty India
Faizan Abul Qais India
M. Ahmed Mesaik Pakistan
Nizam Uddin Pakistan
Citations per year, relative to Kaïss Aouadi Kaïss Aouadi (= 1×)
peers
Avijit Mazumder
Countries citing papers authored by Kaïss Aouadi
Since
Specialization
Citations
This map shows the geographic impact of Kaïss Aouadi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kaïss Aouadi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kaïss Aouadi more than expected).
Fields of papers citing papers by Kaïss Aouadi
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Kaïss Aouadi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kaïss Aouadi. The network helps show where Kaïss Aouadi may publish in the future.
Co-authorship network of co-authors of Kaïss Aouadi
This figure shows the co-authorship network connecting the top 25 collaborators of Kaïss Aouadi. A scholar is included among the top collaborators of Kaïss Aouadi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kaïss Aouadi. Kaïss Aouadi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Alhagri, Ibrahim A., et al.. (2025). Comprehensive multispectral and computational study of isoxazolidine derivative ‘ISoXD3’: Synthesis, spectral characteristics, DNA binding, and comparative effects of allyl and propargyl groups on optical properties. Results in Chemistry. 14. 102080–102080.
2.
Oliveira, Mozaniel Santana de, Suhaila Mohamed, Ashraf N. Abdalla, et al.. (2025). Untargeted metabolomics approach based on UPLC-ESI-QTOF-MS/MS and evaluation of antioxidant and cytotoxic activities of Nepeta deflersiana Schweinf. ex Hedge supported by molecular modeling and ADMET analysis. Journal of Molecular Structure. 1333. 141767–141767.
3.
Ghannay, Siwar, Ibrahim A. Alhagri, Béchir Hammami, et al.. (2024). Synthesis, optical properties, DNA, β-cyclodextrin interaction, hydrogen isotope sensor and computational study of new enantiopure isoxazolidine derivative (ISoXD). Heliyon. 10(4). e26341–e26341.
4.
Ghannay, Siwar, et al.. (2024). Design, synthesis, biological evaluation, kinetic studies and molecular modeling of imidazo-isoxazole derivatives targeting both α-amylase and α-glucosidase inhibitors. Heliyon. 10(20). e38376–e38376.
5.
Ghannay, Siwar, Iqrar Ahmad, Abuzar E. A. E. Albadri, et al.. (2024). Identification of dual-target isoxazolidine-isatin hybrids with antidiabetic potential: Design, synthesis, in vitro and multiscale molecular modeling approaches. Heliyon. 10(4). e25911–e25911.
6.
Alhagri, Ibrahim A., Siwar Ghannay, Sadeq M. Al‐Hazmy, et al.. (2024). Synthesis, optical properties, DNA, β-cyclodextrin interactions, and antioxidant evaluation of novel isoxazolidine derivative (ISoXD2): A multispectral and computational analysis. Heliyon. 10(14). e34561–e34561.
7.
Alminderej, Fahad M., Siwar Ghannay, Béchir Hammami, et al.. (2024). In Silico Design, Synthesis, and Evaluation of Novel Enantiopure Isoxazolidines as Promising Dual Inhibitors of α-Amylase and α-Glucosidase. Molecules. 29(2). 305–305.
8.
Snoussi, Mejdi, Emira Noumi, El Hassane Anouar, et al.. (2023). Phytochemical profiling, antimicrobial, antibiofilm, insecticidal, and anti-leishmanial properties of aqueous extract from Juglans regia L. root bark: In vitro and in silico approaches. International Journal of Food Properties. 26(1). 1079–1097.
9.
Snoussi, Mejdi, Emira Noumi, Lamjed Bouslama, et al.. (2022). Phytochemical Profiling of Allium subhirsutum L. Aqueous Extract with Antioxidant, Antimicrobial, Antibiofilm, and Anti-Quorum Sensing Properties: In Vitro and In Silico Studies. Plants. 11(4). 495–495.
10.
Zrieq, Rafat, Mejdi Snoussi, Munazzah Tasleem, et al.. (2022). Repurposing of anisomycin and oleandomycin as a potential anti-(SARS-CoV-2) virus targeting key enzymes using virtual computational approaches. Cellular and Molecular Biology. 67(5). 387–398.
11.
Zrieq, Rafat, Iqrar Ahmad, Mejdi Snoussi, et al.. (2021). Tomatidine and Patchouli Alcohol as Inhibitors of SARS-CoV-2 Enzymes (3CLpro, PLpro and NSP15) by Molecular Docking and Molecular Dynamics Simulations. International Journal of Molecular Sciences. 22(19). 10693–10693.
12.
Papetti, Adele, Emira Noumi, Raffaella Colombo, et al.. (2021). Bioactivities and in silico study of Pergularia tomentosa L. phytochemicals as potent antimicrobial agents targeting type IIA topoisomerase, TyrRS, and Sap1 virulence proteins. Environmental Science and Pollution Research. 28(20). 25349–25367.
13.
Ghannay, Siwar, Mejdi Snoussi, Sabri Messaoudi, Adel Kadri, & Kaïss Aouadi. (2020). Novel enantiopure isoxazolidine and C-alkyl imine oxide derivatives as potential hypoglycemic agents: Design, synthesis, dual inhibitors of α-amylase and α-glucosidase, ADMET and molecular docking study. Bioorganic Chemistry. 104. 104270–104270.
14.
Nasri, Soumaya, Frédérique Loiseau, Florian Molton, et al.. (2020). Effect of the coordination of π-acceptor 4-cyanopyridine ligand on the structural and electronic properties ofmeso-tetra(para-methoxy) andmeso-tetra(para-chlorophenyl) porphyrin cobalt(ii ) coordination compounds. Application in the catalytic degradation of methylene blue dye. RSC Advances. 10(12). 6900–6918.
15.
Othman, Ismail M. M., Mohamed A. M. Gad‐Elkareem, El Hassane Anouar, et al.. (2020). Design, synthesis ADMET and molecular docking of new imidazo[4,5-b]pyridine-5-thione derivatives as potential tyrosyl-tRNA synthetase inhibitors. Bioorganic Chemistry. 102. 104105–104105.
16.
Ghannay, Siwar, et al.. (2017). Stereoselective synthesis of enantiopure N-substituted pyrrolidin-2,5-dione derivatives by 1,3-dipolar cycloaddition and assessment of their in vitro antioxidant and antibacterial activities. Bioorganic & Medicinal Chemistry Letters. 27(11). 2302–2307.
17.
Aouadi, Kaïss, et al.. (2016). A stereoselective method for the synthesis of enantiopure 3-substituted 4-hydroxyproline derivatives via 1,3-dipolar cycloadditions. Comptes Rendus Chimie. 19(8). 933–935.
18.
Cecioni, Samy, Kaïss Aouadi, Sandrine Parrot, et al.. (2015). Novel routes to either racemic or enantiopure α-amino-(4-hydroxy-pyrrolidin-3-yl)acetic acid derivatives and biological evaluation of a new promising pharmacological scaffold. European Journal of Medicinal Chemistry. 98. 237–249.
19.
Barluenga, Sofía, Cuihua Wang, Kaïss Aouadi, et al.. (2009). Inhibition of HSP90 with Pochoximes: SAR and Structure‐Based Insights. ChemBioChem. 10(17). 2753–2759.
20.
Aouadi, Kaïss, et al.. (2006). Cycloadditions of chiral nitrones to racemic 3-substituted butenes: A direct access with kinetic resolution to enantiopure dihydroxylated amino acids. HAL (Le Centre pour la Communication Scientifique Directe).
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.
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