Drugs from the Oceans: Marine Natural Products as Leads for Drug Discovery

被引:84
作者
Altmann, Karl-Heinz [1 ]
机构
[1] ETH, Dept Chem & Appl Biosci, Inst Pharmaceut Sci, Vladimir Prelog Wag 4,HCI H 405, CH-8093 Zurich, Switzerland
关键词
Clinical development; Drug discovery; Marine natural products; Marine organisms; Medicinal chemistry; Organic synthesis; Semisynthesis; BIOLOGICAL EVALUATION; TUMOR MICROENVIRONMENT; PROTEASOME INHIBITORS; ANTINEOPLASTIC AGENTS; HALICHONDRIN-B; DOLASTATIN; 10; SPONGE; SALINOSPORAMIDE; TUBULIN; BINDING;
D O I
10.2533/chimia.2017.646
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The marine environment harbors a vast number of species that are the source of a wide array of structurally diverse bioactive secondary metabolites. At this point in time, roughly 27'000 marine natural products are known, of which eight are (were) at the origin of seven marketed drugs, mostly for the treatment of cancer. The majority of these drugs and also of drug candidates currently undergoing clinical evaluation (excluding anti-body- drug conjugates) are unmodified natural products, but synthetic chemistry has played a central role in the discovery and/or development of all but one of the approved marine-derived drugs. More than 1000 new marine natural products have been isolated per year over the last decade, but the pool of new and unique structures is far from exhausted. To fully leverage the potential offered by the structural diversity of marine-produced secondary metabolites for drug discovery will require their broad assessment for different bioactivities and the productive interplay between new fermentation technologies, synthetic organic chemistry, and medicinal chemistry, in order to secure compound supply and enable lead optimization.
引用
收藏
页码:646 / 652
页数:7
相关论文
共 78 条
[1]   Diversity, abundance and natural products of marine sponge-associated actinomycetes [J].
Abdelmohsen, Usama Ramadan ;
Bayer, Kristina ;
Hentschel, Ute .
NATURAL PRODUCT REPORTS, 2014, 31 (03) :381-399
[2]  
BAI R, 1991, J BIOL CHEM, V266, P15882
[3]   DOLASTATIN-10, A POWERFUL CYTOSTATIC PEPTIDE DERIVED FROM A MARINE ANIMAL - INHIBITION OF TUBULIN POLYMERIZATION MEDIATED THROUGH THE VINCA ALKALOID BINDING DOMAIN [J].
BAI, R ;
PETTIT, GR ;
HAMEL, E .
BIOCHEMICAL PHARMACOLOGY, 1990, 39 (12) :1941-1949
[4]   The Therapeutic Potential of α7 Nicotinic Acetylcholine Receptor (α7 nAChR) Agonists for the Treatment of the Cognitive Deficits Associated with Schizophrenia [J].
Beinat, Corinne ;
Banister, Samuel D. ;
Herrera, Marco ;
Law, Vivian ;
Kassiou, Michael .
CNS DRUGS, 2015, 29 (07) :529-542
[5]   Rapamycin passes the torch: a new generation of mTOR inhibitors [J].
Benjamin, Don ;
Colombi, Marco ;
Moroni, Christoph ;
Hall, Michael N. .
NATURE REVIEWS DRUG DISCOVERY, 2011, 10 (11) :868-880
[6]   CONTRIBUTIONS TO THE STUDY OF MARINE PRODUCTS .32. THE NUCLEOSIDES OF SPONGES .1. [J].
BERGMANN, W ;
FEENEY, RJ .
JOURNAL OF ORGANIC CHEMISTRY, 1951, 16 (06) :981-987
[7]   CONTRIBUTIONS TO THE STUDY OF MARINE PRODUCTS .39. THE NUCLEOSIDES OF SPONGES .3. SPONGOTHYMIDINE AND SPONGOURIDINE [J].
BERGMANN, W ;
BURKE, DC .
JOURNAL OF ORGANIC CHEMISTRY, 1955, 20 (11) :1501-1507
[8]   Spongosine Production by a Vibrio harveyi Strain Associated with the Sponge Tectitethya crypta [J].
Bertin, Matthew J. ;
Schwartz, Sarah L. ;
Lee, John ;
Korobeynikov, Anton ;
Dorrestein, Pieter C. ;
Gerwick, Lena ;
Gerwick, William H. .
JOURNAL OF NATURAL PRODUCTS, 2015, 78 (03) :493-499
[9]   Marine natural products [J].
Blunt, John W. ;
Copp, Brent R. ;
Keyzers, Robert A. ;
Munro, Murray H. G. ;
Prinsep, Michele R. .
NATURAL PRODUCT REPORTS, 2017, 34 (03) :235-294
[10]   Marine natural products [J].
Blunt, John W. ;
Copp, Brent R. ;
Keyzers, Robert A. ;
Munro, Murray H. G. ;
Prinsep, Michele R. .
NATURAL PRODUCT REPORTS, 2016, 33 (03) :382-431