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用于疟疾化学预防的新药研发。

Development of new drugs for chemoprophylaxis of malaria.

作者信息

Milhous W

机构信息

Walter Reed Army Institute of Research, Washington DC, USA.

出版信息

Bull Soc Pathol Exot. 2001 Jul;94(2 Pt 2):149-51.

Abstract

When U.S. troops first encountered drug resistant malaria during the Vietnam war, the United States Army responded by establishing a malaria drug research program. In 1988, the Walter Reed Army Institute of Research developed mefloquine (WR 149240) and halofantrine (WR 171669). Actually in association with SmithKline Beecham, the WRAIR is developing tafenoquine (WR 238605), an analogue of primaquine, which is expected to be effective in both preventing and treating malaria in deployed military personnel. Final phase III studies leading to U.S. Food and Drug Administration approval are planned for 2000. Applied research is also carried out with the association atovaquone-proguanil (Malarone) or with azithromycin, but also with primaquine, the associations paludrine-dapsone or lapudrine-dapsone, analogues of floxacrine (WR 243251), and a guanylhydrazone (WR 182393). The future scientific directions must focus on basic and applied research for a better understanding of the modes of action and mechanisms of resistance to standard and developmental drugs. Using new techniques, the design and synthesis of new drugs would hopefully result in the development of drugs that circumvent the malaria parasites elusive mechanisms of drug resistance.

摘要

美军在越战期间首次遭遇耐药性疟疾时,美国陆军通过设立疟疾药物研究项目做出了回应。1988年,沃尔特·里德陆军研究所研发出甲氟喹(WR 149240)和卤泛群(WR 171669)。实际上,沃尔特·里德陆军研究所与史克必成公司合作,正在研发磷酸萘喹(WR 238605),它是伯氨喹的类似物,预计对预防和治疗部署在海外的军事人员的疟疾有效。计划于2000年开展最终的三期研究,以获得美国食品药品监督管理局的批准。还与阿托伐醌-氯胍(马拉隆)或阿奇霉素联合开展应用研究,同时也与伯氨喹、氯胍-氨苯砜或拉布喹-氨苯砜联合开展研究,以及研发氟甲喹类似物(WR 243251)和一种脒腙(WR 182393)。未来的科学方向必须聚焦于基础研究和应用研究,以便更好地理解标准药物和正在研发药物的作用方式及耐药机制。利用新技术进行新药的设计与合成,有望开发出能够规避疟原虫难以捉摸的耐药机制的药物。

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