Drug development from marine natural products

被引:857
作者
Molinski, Tadeusz F. [1 ,2 ]
Dalisay, Doralyn S. [1 ,2 ]
Lievens, Sarah L. [1 ,2 ,3 ]
Saludes, Jonel P. [1 ,2 ,3 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[3] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
PHASE-II TRIAL; LARGE-SCALE SYNTHESIS; MICROTUBULE-STABILIZING AGENT; CALCIUM-CHANNEL BLOCKER; PROTEIN-KINASE-C; MOLLUSK ELYSIA-RUFESCENS; OMEGA-CONOTOXIN MVIIA; NON-HODGKINS-LYMPHOMA; SPONGE PHORBAS SP; CELL LUNG-CANCER;
D O I
10.1038/nrd2487
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Drug discovery from marine natural products has enjoyed a renaissance in the past few years. Ziconotide (Prialt; Elan Pharmaceuticals), a peptide originally discovered in a tropical cone snail, was the first marine-derived compound to be approved in the United States in December 2004 for the treatment of pain. Then, in October 2007, trabectedin (Yondelis; PharmaMar) became the first marine anticancer drug to be approved in the European Union. Here, we review the history of drug discovery from marine natural products, and by describing selected examples, we examine the factors that contribute to new discoveries and the difficulties associated with translating marine-derived compounds into clinical trials. Providing an outlook into the future, we also examine the advances that may further expand the promise of drugs from the sea.
引用
收藏
页码:69 / 85
页数:17
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