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Antiplasmodial marine natural products in the perspective of current chemotherapy and prevention of malaria. A review.

机译:从目前的化学疗法和预防疟疾的角度来看抗疟原虫的海洋天然产物。回顾。

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摘要

The difficulty of obtaining an antimalarial vaccine along traditional lines, because of the highly adaptive character of the malaria parasite, prompts a ceaseless need for new drugs. To this end, marine organisms have been explored recently, as reviewed in this article within the perspective of clinically available antimalarial drugs and promising candidates. Most promising are tetrahydropyrrolo[1,2- alpha ]pyrimidinium, bis-indole, and C11-N5 alkaloids from sponges; pyridoacridone and decahydroquinoline alkaloids from ascidians; and pyrrole alkaloids from fungi, as well as polycyclic polyketides, norditerpene, and polyketide endoperoxides, terpene isonitriles and, particularly, mixed-biogenesis alpha -galactosyl ceramides from sponges. The first and the latter classes of agents best fulfill the requirements for combinatorial synthesis in providing a wide variety of compounds for high-throughput screening and toxicity tests. These results came largely from nonprofit organizations, a trend that we foresee will continue. However, partnership with the pharmaceutical industry was and is needed to bring candidate drugs to the clinic. In any event, success will not be achieved without political plans to make the results of technology easily available to poor populations..
机译:由于疟原虫的高度适应性,难以沿传统途径获得抗疟疾疫苗,这促使人们对新药的需求不断增长。为此,最近对海洋生物进行了研究,如本文在临床可用的抗疟药和有前途的候选药物的观点中所概述的。最有希望的是海绵中的四氢吡咯并[1,2-α]嘧啶鎓,双吲哚和C11-N5生物碱。来自海鞘的吡啶ac啶酮和十氢喹啉生物碱;真菌的吡咯生物碱,以及多环聚酮化合物,降冰片烯和聚酮化合物内过氧化物,萜烯异腈,尤其是海绵混合生物发生的α-半乳糖基神经酰胺。在提供用于高通量筛选和毒性测试的各种化合物中,第一类和第二类试剂最能满足组合合成的要求。这些结果主要来自非营利组织,我们预计这一趋势将继续。但是,过去和现在都需要与制药行业建立伙伴关系,以将候选药物带入诊所。无论如何,没有政治计划使贫困人口容易获得技术成果,就不会取得成功。

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