Chemical diversity of bioactive marine natural products: An illustrative case study

被引:39
作者
Costantino, V [1 ]
Fattorusso, E [1 ]
Menna, M [1 ]
Taglialatela-Scafati, O [1 ]
机构
[1] Univ Naples Federico II, Dipartimento Chim Sostanze Nat, I-80131 Naples, Italy
关键词
Marine; chemical diversity; bioactive natural products; glycolipids; alkaloids; polyketides; Plakortis simplex; review;
D O I
10.2174/0929867043364973
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The marine environment contains a number of plants, animals and micro organisms, which, due to the unique adaptations to their habitat, elaborate a wide diversity of natural products with specific bioactivities. These products provide a rich source of chemical diversity that can be used to design and develop new potentially useful therapeutic agents. The huge variety of the structures present in marine organisms has been illustrated through the case study of the sponge Plakortis simplex, whose chemical analysis, started in our laboratories about ten years ago, revealed an incredible variety and abundance of secondary metabolites. The obtained results have been presented with the intention of drawing some conclusions of general relevance. Particularly, the problem of the limited availability of natural compounds for both structural and preliminary pharmacological studies has been discussed, this issue becoming a serious obstacle when the pharmacological research reaches a more advanced stage. Furthermore, the origin of the chemodiversity in Plakortis simplex and, in general, in marine invertebrates has been discussed; in this respect, the possible cooperative role of symbiotic micro-organisms in the biosynthesis of the varied metabolic content typical of these organisms has been considered.
引用
收藏
页码:1671 / 1692
页数:22
相关论文
共 108 条
[81]   Haplosamates A and B: New steroidal sulfamate esters from two haplosclerid sponges [J].
Qureshi, A ;
Faulkner, DJ .
TETRAHEDRON, 1999, 55 (28) :8323-8330
[82]   THE BIOSYNTHESIS OF TRITERPENOIDS OF THE HOPANE SERIES IN THE EUBACTERIA - A MINE OF NEW ENZYME-REACTIONS [J].
ROHMER, M .
PURE AND APPLIED CHEMISTRY, 1993, 65 (06) :1293-1298
[83]  
SACHLER O, 1980, NATURFORSCH C BIOS C, V35, P340
[84]   Cytotoxic β-carbolines and cyclic peroxides from the palauan sponge Plakortis nigra [J].
Sandler, JS ;
Colin, PL ;
Hooper, JNA ;
Faulkner, DJ .
JOURNAL OF NATURAL PRODUCTS, 2002, 65 (09) :1258-1261
[85]   MARINE NATURAL-PRODUCTS - HALITOXIN, TOXIC COMPLEX OF SEVERAL MARINE SPONGES OF GENUS HALICLONA [J].
SCHMITZ, FJ ;
HOLLENBEAK, KH ;
CAMPBELL, DC .
JOURNAL OF ORGANIC CHEMISTRY, 1978, 43 (20) :3916-3922
[86]   Novel bacterial triterpenoids of the hopane series from Nitrosomonas europaea and their significance for the formation of the C35 bacteriohopane skeleton [J].
Seemann, M ;
Bisseret, P ;
Tritz, JP ;
Hooper, AB ;
Rohmer, M .
TETRAHEDRON LETTERS, 1999, 40 (09) :1681-1684
[87]  
Silva CJ, 2001, DRUGS PHARM SCI, V114, P357
[88]   METABOLITES OF 3 MARINE SPONGES OF THE GENUS PLAKORTIS [J].
STIERLE, DB ;
FAULKNER, DJ .
JOURNAL OF ORGANIC CHEMISTRY, 1980, 45 (17) :3396-3401
[89]   The role of natural products in a modern drug discovery program [J].
Strohl, WR .
DRUG DISCOVERY TODAY, 2000, 5 (02) :39-41
[90]  
SWEELEY CC, 1972, METHODS CARBOHYDRATE, V6