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"dihydroartemisinin"

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"dihydroartemisinin"

Original Article

Antimalarial Efficacy of Aqueous Extract of Strychnos ligustrina and Its Combination with Dihydroartemisinin and Piperaquine Phosphate (DHP) against Plasmodium berghei Infection
Umi Cahyaningsih, Siti Sa’diah, Wasrin Syafii, Rita Kartika Sari, Abdul Jafar Maring, Arifin Budiman Nugraha
Korean J Parasitol 2022;60(5):339-344.
Published online October 21, 2022
DOI: https://doi.org/10.3347/kjp.2022.60.5.339
The development of drug resistance is one of the most severe concerns of malaria control because it increases the risk of malaria morbidity and death. A new candidate drug with antiplasmodial activity is urgently needed. This study evaluated the efficacy of different dosages of aqueous extract of Strychnos ligustrina combined with dihydroartemisinin and piperaquine phosphate (DHP) against murine Plasmodium berghei infection. The BALB/c mice aged 6-8 weeks were divided into 6 groups, each consisting of 10 mice. The growth inhibition of compounds against P. berghei was monitored by calculating the percentage of parasitemia. The results showed that the mice receiving aqueous extract and combination treatment showed growth inhibition of P. berghei in 74% and 94%, respectively. S. ligustrina extract, which consisted of brucine and strychnine, effectively inhibited the multiplication of P. berghei. The treated mice showed improved hematology profiles, body weight, and temperature, as compared to control mice. Co-treatment with S. ligustrina extract and DHP revealed significant antimalarial and antipyretic effects. Our results provide prospects for further discovery of antimalarial drugs that may show more successful chemotherapeutic treatment.

Citations

Citations to this article as recorded by  Crossref logo
  • In Vitro and Molecular Docking Studies of the Antimalarial Activities of Strychnos ligustrina Extracts from Different Parts of the Woody Stem
    Rita Kartika SARI, Wasrin SYAFII, Yanico Hadi PRAYOGO, Anne CAROLINA, Sri FAMILASARI, Umi CAHYANINGSIH, Siti SA’DIAH, Setyanto Tri WAHYUDI, Muhammad Adly Rahandi LUBIS
    Journal of the Korean Wood Science and Technology.2025; 53(1): 89.     CrossRef
  • Antimalarial drug resistance and drug discovery: learning from the past to innovate the future
    Liana Theodoridis, Teresa G. Carvalho
    International Journal for Parasitology: Drugs and Drug Resistance.2025; 28: 100602.     CrossRef
  • Chemical constituents, pharmacological action, antitumor application, and toxicity of Strychnine Semen from Strychnons pierriana A.W.Hill.: A review
    Weiran Liu, Xintian Tang, Chengyu Fan, Guannan He, Xiaoxin Wang, Xiaodong Liang, Xia Bao
    Journal of Ethnopharmacology.2023; 317: 116748.     CrossRef
  • 3,536 View
  • 176 Download
  • 3 Web of Science
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Brief Communications
Antimalarial Activity of C-10 Substituted Triazolyl Artemisinin
Gab-Man Park, Hyun Park, Sangtae Oh, Seokjoon Lee
Korean J Parasitol 2017;55(6):661-665.
Published online December 31, 2017
DOI: https://doi.org/10.3347/kjp.2017.55.6.661
We synthesized C-10 substituted triazolyl artemisinins by the Huisgen cycloaddition reaction between dihydroartemisinins (2) and variously substituted 1, 2, 3-triazoles (8a-8h). The antimalarial activities of 32 novel artemisinin derivatives were screened against a chloroquine-resistant parasite. Among them, triazolyl artemisinins with electron-withdrawing groups showed stronger antimalarial activities than those shown by the derivatives having electron-donating groups. In particularly, m-chlorotriazolyl artemisinin (9d-12d) showed antimalarial activity equivalent to that of artemisinin and could be a strong drug candidate.

Citations

Citations to this article as recorded by  Crossref logo
  • Novel frontiers through nitrogen substitution at 6th, 10th and 11th position of artemisinin: Synthetic approaches and antimalarial activity
    Priyanka Yadav, Varun Rawat, Shalini Kaushik Love, Ved Prakash Verma
    European Journal of Medicinal Chemistry.2025; 281: 117032.     CrossRef
  • Identification of potential bi-triazole based antimalarial compounds and their effects against asexual stages of Plasmodium isolates
    Marcinete Latorre Almeida, Leandro do Nascimento Martinez, Welington da Silva Paula do Nascimento, Guilherme Matos Passarini, Daniel Sol Sol de Medeiros, Minelly Azevedo da Silva, Saara Neri Fialho, Amália do Santos Ferreira, Norton Rubens Diunior Lucas P
    Caderno Pedagógico.2024; 21(13): e12709.     CrossRef
  • In silico screening, synthesis, and antimalarial evaluation of PABA substituted 1,3,5-triazine derivatives as Pf-DHFR inhibitors
    Ashmita Saha, Ayesha Aktar Khanam Choudhury, Nayana Adhikari, Surajit Kumar Ghosh, Anshul Shakya, Saurav Jyoti Patgiri, Udaya Pratap Singh, Hans Raj Bhat
    Experimental Parasitology.2023; 250: 108546.     CrossRef
  • Current development of 1,2,3-triazole derived potential antimalarial scaffolds: Structure- activity relationship (SAR) and bioactive compounds
    S. Maheen Abdul Rahman, Jasvinder Singh Bhatti, Suresh Thareja, Vikramdeep Monga
    European Journal of Medicinal Chemistry.2023; 259: 115699.     CrossRef
  • Exploration of artemisinin derivatives and synthetic peroxides in antimalarial drug discovery research
    Om P.S. Patel, Richard M. Beteck, Lesetja J. Legoabe
    European Journal of Medicinal Chemistry.2021; 213: 113193.     CrossRef
  • 7,569 View
  • 170 Download
  • 6 Web of Science
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Antimalarial activity of thiophenyl- and benzenesulfonyl-dihydroartemisinin
Seokjoon Lee, Sangtae Oh, Gab-Man Park, Tong-Soo Kim, Jae-Sook Ryu, Han-Kyu Choi
Korean J Parasitol 2005;43(3):123-126.
Published online September 20, 2005
DOI: https://doi.org/10.3347/kjp.2005.43.3.123

Each diastereomer of 10-thiophenyl- and 10-benzenesulfonyl-dihydroartemisinin was synthesized from artemisinin in three steps, and screened against chloroquine-resistance and chloroquine-sensitive Plasmodium falciparum. Three of the four tested compounds were found to be effective. Especially, 10β-benzenesulfonyl-dihydroartemisinin showed stronger antimalarial activity than artemisinin.

Citations

Citations to this article as recorded by  Crossref logo
  • Chemical transformations of artemisinin
    A. V. Semakov, S. V. Afanasyeva, S. A. Pukhov
    Russian Chemical Bulletin.2024; 74(6): 1604.     CrossRef
  • Design, synthesis and molecular docking studies of novel N-arylsulfonyl-benzimidazoles with anti Trypanosoma cruzi activity
    Gisele E. Miana, Sergio R. Ribone, Domingo M.A. Vera, Manuel Sánchez-Moreno, María R. Mazzieri, Mario A. Quevedo
    European Journal of Medicinal Chemistry.2019; 165: 1.     CrossRef
  • Antimalarial Activity of C-10 Substituted Triazolyl Artemisinin
    Gab-Man Park, Hyun Park, Sangtae Oh, Seokjoon Lee
    The Korean Journal of Parasitology.2017; 55(6): 661.     CrossRef
  • TD-DFT calculations of UV absorption bands and their intensities in the spectra of some tetrahydroquinolines
    María V. Cooke, Ivana Malvacio, Walter J. Peláez, Ana J. Pepino, María R. Mazzieri, Gustavo A. Argüello
    RSC Advances.2015; 5(33): 26255.     CrossRef
  • Malaria-Infected Mice Live Until at Least Day 30 after a New Artemisinin-Derived Thioacetal Thiocarbonate Combined with Mefloquine Are Administered Together in a Single, Low, Oral Dose
    Alexander M. Jacobine, Jennifer R. Mazzone, Rachel D. Slack, Abhai K. Tripathi, David J. Sullivan, Gary H. Posner
    Journal of Medicinal Chemistry.2012; 55(17): 7892.     CrossRef
  • Synthesis, stereoelectronic characterization and antiparasitic activity of new 1-benzenesulfonyl-2-methyl-1,2,3,4-tetrahydroquinolines
    Romina J. Pagliero, Sabrina Lusvarghi, Adriana B. Pierini, Reto Brun, María R. Mazzieri
    Bioorganic & Medicinal Chemistry.2010; 18(1): 142.     CrossRef
  • 7,794 View
  • 99 Download
  • Crossref