Recent approaches in the drug research and development of novel antimalarial drugs with new targets.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Pub Date : 2023-03-01 DOI:10.2478/acph-2023-0001
Naveen Kumar Reddy Chinnappanna, Gopi Yennam, Chaitanya Budagam Haima Naga Venkata Chaitanya, Shinu Pottathil, Pobitra Borah, Katharigatta N Venugopala, Pran Kishore Deb, Raghu Prasad Mailavaram
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引用次数: 3

Abstract

Malaria is a serious worldwide medical issue that results in substantial annual death and morbidity. The availability of treatment alternatives is limited, and the rise of resistant parasite types has posed a significant challenge to malaria treatment. To prevent a public health disaster, novel antimalarial agents with single-dosage therapies, extensive curative capability, and new mechanisms are urgently needed. There are several approaches to developing antimalarial drugs, ranging from alterations of current drugs to the creation of new compounds with specific targeting abilities. The availability of multiple genomic techniques, as well as recent advancements in parasite biology, provides a varied collection of possible targets for the development of novel treatments. A number of promising pharmacological interference targets have been uncovered in modern times. As a result, our review concentrates on the most current scientific and technical progress in the innovation of new antimalarial medications. The protein kinases, choline transport inhibitors, dihydroorotate dehydrogenase inhibitors, isoprenoid biosynthesis inhibitors, and enzymes involved in the metabolism of lipids and replication of deoxyribonucleic acid, are among the most fascinating antimalarial target proteins presently being investigated. The new cellular targets and drugs which can inhibit malaria and their development techniques are summarised in this study.

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具有新靶点的新型抗疟药物研究和开发的最新途径。
疟疾是一个严重的世界性医疗问题,每年造成大量死亡和发病率。可获得的治疗方法有限,而且耐药寄生虫类型的增加对疟疾治疗构成了重大挑战。为了预防公共卫生灾难,迫切需要具有单剂量治疗、广泛治疗能力和新机制的新型抗疟药。开发抗疟疾药物有几种方法,从改变现有药物到创造具有特定靶向能力的新化合物。多种基因组技术的可用性,以及寄生虫生物学的最新进展,为开发新的治疗方法提供了各种可能的靶点。现代已经发现了许多有前途的药理干扰靶点。因此,我们的综述集中在新的抗疟药物创新方面的最新科学技术进展。蛋白激酶、胆碱转运抑制剂、二氢乳酸脱氢酶抑制剂、类异戊二烯生物合成抑制剂以及参与脂质代谢和脱氧核糖核酸复制的酶是目前正在研究的最令人着迷的抗疟疾靶蛋白。本文综述了新的抑制疟疾的细胞靶点和药物及其开发技术。
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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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