Mapping the Landscape of Recent Studies on Pyrimidine Derivatives as Antimicrobial Agents: A Bibliometric Analysis
Main Article Content
Abstract
Background: Recently, microbes have become resistant to various drugs and this resistance is considered a big challenge in the treatment of infectious diseases. Therefore, there is a fundamental need to develop new drugs to treat resistant microbes. Having different biological effects, pyrimidine is an effective ring in the structure of drugs with antimicrobial effects. There hasn't been a bibliometric analysis in this area despite the field's incredible progress in the last 10 years in the study of pyrimidine as an antimicrobial agent.
Methods: A comprehensive examination of the available literature published between 2015 and 2023 on pyrimidine derivatives as antimicrobial agents was done across the Scopus database. Microsoft Excel 365 was employed to analyze the quantitative variables, such as publications and citation counts, for the authors, institutions, countries, and journals, the powerful tool. Furthermore, the network visualization and analysis of co-authorship, co-occurrence, and co-citation among countries, institutions, authors, and keywords were facilitated by VOSviewer.
Results: A total of 934 articles were selected for the study. The years 2019 and 2022 exhibited the highest volume of published papers on pyrimidine derivatives as antimicrobial agents between 2015 and 2023, with 125 publications each. A total of 53 countries contributed to the topic, with India leading in publications, followed by Egypt, China, Saudi Arabia, and the United States. Among journals, the Journal of Heterocyclic Chemistry had the highest number of publications (n=50), followed by the European Journal of Medicinal Chemistry with 37 publications.
Conclusion: The findings provide valuable insights for researchers in selecting specific compounds for their upcoming studies, emphasizing the significance of bibliometric analysis in shaping the trajectory of research in the field of pyrimidine antimicrobial research.
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References
Zhuang J., Ma S. Recent development of pyrimidine-containing antimicrobial agents. ChemMedChem. 2020;15(20):1875-86.
Mallikarjunaswamy C, Mallesha L, Bhadregowda DG, and Pinto O. Studies on the synthesis of pyrimidine derivatives and their antimicrobial activity. Arab J Chem. 2017;10:S484-90. Available from: http://dx.doi.org/10.1016/j.arabjc.2012.10.008
Zarenezhad E, Farjam M, and Iraji A. Synthesis and biological activity of pyrimidine-containing hybrids: Focusing on pharmacological application. J Mol Struct. 2021;1230.
Sharma V, Chitranshi N, and Agarwal AK. Significance and biological importance of pyrimidine in the microbial world. Int J Med Chem. 2014;2014:1-31.
Kumar S., Narasimhan B. Therapeutic potential of heterocyclic pyrimidine scaffolds. Chem Cent J. 2018;12.
Vasanthi R., Balamurugan V. A review of the pharmacological aspects of Canavalia rosea. Sci Prog Res. 2022;2(2):567–79.
Alam M, Kobir ME, Kumer A, Chakma U, Akter P, and Bhuiyan MMH. Antibacterial, antifungal, and antiviral activities of pyrimido[4,5-d]pyrimidine derivatives through computational approaches. Org Commun. 2022;15(3):239–60.
Elbadawy M., Ishihara Y., Aboubakr M., Sasaki K., and Shimoda M. Oral absorption profiles of sulfonamides in Shiba goats: a comparison among sulfadimidine, sulfadiazine, and sulfanilamide. J Vet Med Sci. 2016;78(6):1025–9.
Pontikis R, Benhida R, Aubertin AM, Grierson DS, and Monneret C. Synthesis and anti-HIV activity of novel N-1 side chain-modified analogs of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT). J Med Chem. 1997;40(12):1845–53.
Gadhachanda VR, Wu B, Wang Z, Kuhen KL, Caldwell J, Zondler H, et al. 4-Aminopyrimidines as novel HIV-1 inhibitors. Bioorg Med Chem Lett. 2007;17:260–5.
Rashid HU, Martines MAU, Duarte AP, Jorge J., Rasool S., Muhammad R., et al. Research developments in the syntheses, anti-inflammatory activities, and structure-activity relationships of pyrimidines. RSC Adv. 2021;11(11):6060–98.
El-Mekabaty A, El-Shora HM. Synthesis and evaluation of some novel 3-hetarylindole derivatives as antimicrobial and antioxidant agents. Chem Heterocycl Compd. 2018;54(6):618–24.
Kostova I, Atanasov PY. Antioxidant properties of pyrimidine and uracil derivatives. Curr Org Chem. 2017;21(20).
Alam O, Khan SA, Siddiqui N, Ahsan W, Verma SP, and Gilani SJ. Antihypertensive activity of newer 1,4-dihydro-5-pyrimidine carboxamides: Synthesis and pharmacological evaluation. Eur J Med Chem. 2010;45(11):5113–9. Available from: http://dx.doi.org/10.1016/j.ejmech.2010.08.022
Patel AA, Mehta AG. Synthesis and characterization of some pyrimidine-quinoline clubbed molecules and their microbicidal efficacy. J Saudi Chem Soc. 2010;14(2):203–8. Available from: http://dx.doi.org/10.1016/j.jscs.2010.02.012
Bhat AR. Biological activity of pyrimidine derivatives: A review. Org Med Chem IJ. 2017;2(2):1-4.
Vale N., Ferreira A., Matos J., Fresco P., and Gouveia MJ. Amino acids in the development of prodrugs. Molecules. 2018;23(9).
Ramirez-Malule H, Cardona-G W. Bibliometric analysis of recent research on 5-fluorouracil (2015–2020). J Appl Pharm Sci. 2022;12(1):70–7.
Dede E., Ozdemir E. Mapping and performance evaluation of mathematics education research in Turkey: A bibliometric analysis from 2005 to 2021. J Pedagog Res. 2022;6(4):1-19.
Donthu N, Kumar S, Mukherjee D, Pandey N, and Lim WM. How to conduct a bibliometric analysis: an overview and guidelines. J Bus Res. 2021;133:285–96. Available from: https://doi.org/10.1016/j.jbusres.2021.04.070
Jadhav PA, Baravkar A. Recent advances in the antimicrobial activity of pyrimidines: a review. Asian J Pharm Clin Res. 2022;15(2):4-10.
Bu YY, Yamazaki H, Ukai K, and Namikoshi M. Anti-mycobacterial nucleoside antibiotics from a marine-derived Streptomyces sp. TPU1236A. Mar Drugs. 2014;12:6102-12.
Larwood DJ. Nikkomycin Z—ready to meet the promise? J Fungi. 2020;6:1–14.
Gomha SM, El-Idreesy TT, Mabrouk BK, and Sayed AR. Synthesis and characterization of new pyrido-thieno-pyrimidine derivatives incorporating the pyrazole moiety. Synth Commun. 2017;47(23):2232-8.
Kappe OC. 100 years of the Biginelli dihydropyrimidine synthesis. Tetrahedron. 1993;49:6937-63.
Wu H, Tong L, Wang Y, Yan H, and Sun Z. Bibliometric analysis of global research trends on ultrasound microbubbles: a quickly developing field. Front Pharmacol. 2021;12.