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Research Articles

Elucidation of the anti-plasmodial activity of novel imidazole and oxazole compounds through computational and in vivo experimental approaches

, , , , , , , , , , & ORCID Icon show all
Pages 9013-9021 | Received 28 Jul 2022, Accepted 19 Oct 2022, Published online: 30 Oct 2022

References

  • Adegboyega, A. E., Johnson, T. O., & Omale, S. (2021). Computational modeling of the pharmacological actions of some antiviral agents against SARS-CoV-2. In Data science for COVID-19. Elsevier Inc. https://doi.org/10.1016/b978-0-12-824536-1.00018-6
  • Adeyemi, O. S., Eseola, A. O., Plass, W., Atolani, O., Sugi, T., Han, Y., Batiha, G. E., Kato, K., Awakan, O. J., Olaolu, T. D., Nwonuma, C. O., Alejolowo, O., Owolabi, A., Rotimi, D., & Kayode, O. T. (2020). Imidazole derivatives as antiparasitic agents and use of molecular modeling to investigate the structure–activity relationship. Parasitology Research, 119(6), 1925–1941. https://doi.org/10.1007/s00436-020-06668-6
  • Arifin, W. N., & Zahiruddin, W. M. (2017). Sample size calculation in animal studies using resource equation approach. Malaysian Journal of Medical Sciences, 24(5), 101–105. https://doi.org/10.21315/mjms2017.24.5.11
  • Baire, B., Gardas, R., & Gandhi, S. (2021). Cycloaddition reactions in ionic liquids for the synthesis of biologically relevant heterocycles. In Green synthetic approaches for biologically relevant heterocycles. Volume 1: Advanced Synthetic Techniques (pp. 249–295). Elsevier. https://doi.org/10.1016/B978-0-12-820586-0.00006-6
  • Bhandari, K., Srinivas, N., Shiva Keshava, G. B., & Shukla, P. K. (2009). Tetrahydronaphthyl azole oxime ethers: The conformationally rigid analogues of oxiconazole as antibacterials. European Journal of Medicinal Chemistry, 44(1), 437–447. https://doi.org/10.1016/j.ejmech.2008.01.006
  • Choi, S., Pradhan, A., Hammond, N. L., Chittiboyina, A. G., Tekwani, B. L., & Avery, M. A. (2007). Design, synthesis, and biological evaluation of Plasmodium falciparum lactate dehydrogenase inhibitors. Journal of Medicinal Chemistry, 50(16), 3841–3850. https://doi.org/10.1021/jm070336k
  • Dacie, J. V., & Lewis, S. M. (2000). Practical haematology (9th ed.). Churchill Livingstone.
  • Emami, S., Foroumadi, A., Falahati, M., Lotfali, E., Rajabalian, S., Ebrahimi, S. A., Farahyar, S., & Shafiee, A. (2008). 2-Hydroxyphenacyl azoles and related azolium derivatives as antifungal agents. Bioorganic & Medicinal Chemistry Letters, 18(1), 141–146. https://doi.org/10.1016/j.bmcl.2007.10.111
  • Guha, M., Kumar, S., Choubey, V., Maity, P., Bandyopadhyay, U., Guha, M., Kumar, S., Choubey, V., Maity, P., & Bandyopadhyay, U. (2006). Apoptosis in liver during malaria: Role of oxidative stress and implication of mitochondrial pathway. FASEB Journal, 20(8), 1224–1226. https://doi.org/10.1096/fj.05-5338fje
  • Iman, M., Davood, A., & Khamesipour, A. (2020). Design of antimalarial agents based on pyrimidine derivatives as methionine aminopeptidase 1b inhibitor: Molecular docking, quantitative structure activity relationships, and molecular dynamics simulation studies. Journal of the Chinese Chemical Society, 67(5), 880–890. https://doi.org/10.1002/jccs.201900165
  • Johnson, T. O., Adegboyega, A. E., Iwaloye, O., Eseola, O. A., Plass, W., Afolabi, B., Rotimi, D., Ahmed, E. I., Albrakati, A., Batiha, G. E., & Adeyemi, O. S. (2021). Computational study of the therapeutic potentials of a new series of imidazole derivatives against SARS-CoV-2. Journal of Pharmacological Sciences, May, 147(1), 62–71. https://doi.org/10.1016/j.jphs.2021.05.004
  • Johnson, T. O., Istifanus, G., & Kutshik, R. J. (2020). In vitro and in vivo analysis of the anti-plasmodial activity of ethanol extract of Phyllanthus nivosus W. Bull leaf. Journal of Parasitic Diseases, 44(1), 166–173. https://doi.org/10.1007/s12639-019-01178-4
  • Johnson, T. O., Odoh, K. D., Nwonuma, C. O., Akinsanmi, A. O., & Adegboyega, A. E. (2020). Biochemical evaluation and molecular docking assessment of the anti-inflammatory potential of Phyllanthus nivosus leaf against ulcerative colitis. Heliyon, 6(5), e03893. https://doi.org/10.1016/j.heliyon.2020.e03893
  • Kakkar, S., & Narasimhan, B. (2019). A comprehensive review on biological activities of oxazole derivatives. BMC Chemistry, 13(1), 1. 24. https://doi.org/10.1186/s13065-019-0531-9
  • Liu, L., Hu, Y., Shen, Y. F., Wang, G. X., & Zhu, B. (2017). Evaluation on antiviral activity of coumarin derivatives against spring viraemia of carp virus in epithelioma papulosum cyprini cells. Antiviral Research, 144, 173–185. https://doi.org/10.1016/j.antiviral.2017.06.007
  • Makler, M. T., & Hinrichs, D. J. (1993). Measurement of the lactate dehydrogenase activity of Plasmodium falciparum as an assessment of parasitemia. The American Journal of Tropical Medicine and Hygiene, 48(2), 205–210. https://doi.org/10.4269/ajtmh.1993.48.205
  • Ojo, O. A., Adegboyega, A. E., Johnson, G. I., Umedum, N. L., Onuh, K., Adeduro, M. N., NwOBodo, V. O., Elekan, A. O., Alemika, T. E., & Johnson, T. O. (2021). Deciphering the interactions of compounds from Allium sativum targeted towards identification of novel PTP 1B inhibitors in diabetes treatment: A computational approach. Informatics in Medicine Unlocked, 26, 100719. https://doi.org/10.1016/j.imu.2021.100719
  • Penna-Coutinho, J., Cortopassi, W. A., Oliveira, A. A., França, T. C. C., & Krettli, A. U. (2011). (2011). Antimalarial activity of potential inhibitors of Plasmodium falciparum lactate dehydrogenase enzyme selected by docking studies. PLoS ONE, 6(7), e21237. https://doi.org/10.1371/journal.pone.0021237A.
  • Pinzi, L., & Rastelli, G. (2019). Molecular docking: Shifting paradigms in drug discovery. International Journal of Molecular Sciences, 20(18), 4331. https://doi.org/10.3390/ijms20184331
  • Raman, N., Mitu, L., Sakthivel, A., & Pandi, M. S. S. (2009). Studies on DNA cleavage and antimicrobial screening of transition metal complexes of 4-aminoantipyrine derivatives of N2O2 type. Journal of the Iranian Chemical Society, 6(4), 738–748. https://doi.org/10.1007/BF03246164
  • Reilly, C. A., & Aust, S. D. (1999). Measurement of lipid peroxidation. In Current protocols in toxicology. Wiley Online Library. https://doi.org/10.1002/0471140856.tx0204s00
  • Samuel, B. B., Oluyemi, W. M., Johnson, T. O., & Adegboyega, A. E. (2021). High-throughput virtual screening with molecular docking, pharmacophore modelling and ADME prediction to discover potential inhibitors of plasmodium falciparum lactate dehydrogenase (PFLDH) from compounds of combretaceae family. Tropical Journal of Natural Product Research, 5(9), 1665–1672. https://doi.org/10.26538/tjnpr/v5i9.22
  • Shadrack, D. M., Nyandoro, S. S., Munissi, J. J. E., & Mubofu, E. B. (2016). In silico evaluation of anti-malarial agents from Hoslundia opposita as inhibitors of plasmodium falciparum lactate dehydrogenase (Pf LDH) enzyme. Computational Molecular Bioscience, 06(02), 23–32. https://doi.org/10.4236/cmb.2016.62002
  • Sharma, D., Narasimhan, B., Kumar, P., Judge, V., Narang, R., De Clercq, E., & Balzarini, J. (2009). Synthesis, antimicrobial and antiviral activity of substituted benzimidazoles. Journal of Enzyme Inhibition and Medicinal Chemistry, 24(5), 1161–1168. https://doi.org/10.1080/14756360802694427
  • WHO (2020). World Malaria Report 2020. World Health Organization. https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2020
  • WHO (2021). World Malaria Report 2021. In Word Malaria report Geneva: World Health Organization. Licence: CC.
  • Wiwanitkit, V. (2007). Plasmodium and host lactate dehydrogenase molecular function and biological pathways: Implication for antimalarial drug discovery. Chemical Biology & Drug Design, 69(4), 280–283. https://doi.org/10.1111/j.1747-0285.2007.00495.x
  • Zakaria, N. H., Hassan, N. I., & Wai, L. K. (2020). Molecular docking study of the interactions between plasmodium falciparum lactate dehydrogenase and 4-aminoquinoline hybrids. Sains Malaysiana, 49(8), 1905–1913. https://doi.org/10.17576/jsm-2020-4908-12

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