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疟原虫中的药物靶点。

Drug targets in malaria parasites.

作者信息

Padmanaban G

机构信息

Department of Biochemistry, Indian Institute of Science, Bangalore 560 012, India.

出版信息

Adv Biochem Eng Biotechnol. 2003;84:123-41. doi: 10.1007/3-540-36488-9_4.

Abstract

Malaria ranks with tuberculosis and AIDS in terms of its ability to destroy human health. In India there are at least two million cases seen annually. Although mortality may not be as high as it is in Africa, the trauma due to morbidity and debility and loss of productive man hours are colossal. Since resistance to chloroquine and antifolates is spreading rapidly, there is need to develop new pharmacophores, for which identification of new drug targets is essential. This review focuses on targets arising from classical and unique metabolic pathways in the malaria parasite, highlighting the research being carried out in India in the context of the global scenario. A significant amount of research in India and elsewhere has provided new knowledge on parasite biology, that could pave the way for the development of new pharmacophores. However, it is a matter of regret to record that malaria being a poor man's disease does not enthuse pharmaceutical companies in general to invest and bring out new molecules. Developing countries like India should take a lead in developing new but affordable antimalarials.

摘要

疟疾在破坏人类健康的能力方面与结核病和艾滋病相当。在印度,每年至少有200万例病例。虽然死亡率可能不像非洲那么高,但发病和身体虚弱所带来的创伤以及生产工时的损失却是巨大的。由于对氯喹和抗叶酸药物的耐药性正在迅速蔓延,因此需要开发新的药效基团,而确定新的药物靶点至关重要。本综述重点关注疟原虫经典和独特代谢途径产生的靶点,突出了在全球背景下印度正在开展的研究。印度和其他地方的大量研究为寄生虫生物学提供了新知识,这可能为新药效基团的开发铺平道路。然而,令人遗憾的是,疟疾是穷人的疾病,总体上并未激发制药公司投资并推出新分子。像印度这样的发展中国家应该带头开发新的但价格可承受的抗疟药物。

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