Shukla Monika, Hassam Mohammad, Kumar Yadav Dinesh, Sharma Siddharth, Singh Chandan, Puri Sunil K, Shrivastava Rahul, Prakash Verma Ved
Department of Chemistry, Banasthali University, Banasthali Newai 304022, Rajasthan, India.
Medicinal & Process Chemistry Division, CSIR-Central Drug Research Institute, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Bioorg Med Chem Lett. 2021 Oct 1;49:128305. doi: 10.1016/j.bmcl.2021.128305. Epub 2021 Aug 6.
Malaria epidemics represent one of the life-threatening diseases to low-income lying countries which subsequently affect the economic and social condition of mankind. In continuation in the development of a novel series of 1,2,4-trioxanes 13a1-c1, 13a2-c2, and 13a3-c3 have been prepared and further converted into their hemisuccinate derivatives 14a1-c1, 14a2-c2, and 14a3-c3 respectively. All these new compounds were evaluated for their antimalarial activity against multidrug-resistant Plasmodium yoelii nigeriensis in mice by both oral and intramuscular (im) routes. Hydroxy-functionalized trioxane 13a1 showed 80% protection and its hemisuccinate derivative 14a1 showed 100% protection at a dose of 48 mg/kg × 4 days by both routes, which is twice active than artemisinin by oral route.
疟疾流行是低收入国家面临的危及生命的疾病之一,进而影响人类的经济和社会状况。作为新型1,2,4-三氧杂环己烷系列(13a1-c1、13a2-c2和13a3-c3)开发工作的延续,已制备出这些化合物,并进一步分别将其转化为半琥珀酸酯衍生物14a1-c1、14a2-c2和14a3-c3。通过口服和肌肉注射(im)途径,对所有这些新化合物针对小鼠体内耐多药约氏疟原虫尼日尔株的抗疟活性进行了评估。羟基官能化三氧杂环己烷13a1在剂量为48 mg/kg×4天时,通过两种途径均显示出80%的保护率,其半琥珀酸酯衍生物14a1通过两种途径在该剂量下均显示出100%的保护率,其口服活性是青蒿素的两倍。