Advanced preclinical and clinical trials of natural products and related compounds from marine sources

被引:132
作者
Newman, DJ [1 ]
Cragg, GM [1 ]
机构
[1] NCI, Nat Prod Branch, Fairview Ctr, Dev Therapeut Program, Frederick, MD 21702 USA
关键词
D O I
10.2174/0929867043364982
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 has proven to be a very rich source of extremely potent compounds that have demonstrated significant activities in anti-tumor, anti-inflammatory, analgesia, immuno-modulation, allergy and anti-viral assays. Although the case can and has been made that the nucleosides such as Ara-A and Ara-C are derived from knowledge gained from investigations of bioactive marine nucleosides, no drug directly from marine sources (whether isolated or by total synthesis) has yet made it to the commercial sector in any human disease. However, as shown in this review, there are now significant numbers of very interesting molecules that have come from marine sources, or have been synthesized as a result of knowledge gained from a prototypical compound, that are either in or approaching Phase III clinical trials in cancer, analgesia and allergy, with a very substantial number of other, quite different potential agents following in their wake, in these and in other diseases.
引用
收藏
页码:1693 / 1713
页数:21
相关论文
共 192 条
[1]   NOVEL SPONGE-DERIVED AMINO-ACIDS .5. STRUCTURES, STEREOCHEMISTRY, AND SYNTHESIS OF SEVERAL NEW HETEROCYCLES [J].
ADAMCZESKI, M ;
QUINOA, E ;
CREWS, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (02) :647-654
[2]   NOVEL SPONGE-DERIVED AMINO-ACIDS .11. THE ENTIRE ABSOLUTE STEREOCHEMISTRY OF THE BENGAMIDES [J].
ADAMCZESKI, M ;
QUINOA, E ;
CREWS, P .
JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (01) :240-242
[3]   Total synthesis of the microtubule stabilizing antitumor agent laulimalide and some nonnatural analogues:: The power of sharpless' asymmetric epoxidation [J].
Ahmed, A ;
Hoegenauer, EK ;
Enev, VAS ;
Hanbauer, M ;
Kaehlig, H ;
Öhler, E ;
Mulzer, J .
JOURNAL OF ORGANIC CHEMISTRY, 2003, 68 (08) :3026-3042
[4]  
AHOND A, 1988, CR ACAD SCI II, V307, P145
[5]   TOTAL SYNTHESIS OF HALICHONDRIN-B AND NORHALICHONDRIN-B [J].
AICHER, TD ;
BUSZEK, KR ;
FANG, FG ;
FORSYTH, CJ ;
JUNG, SH ;
KISHI, Y ;
MATELICH, MC ;
SCOLA, PM ;
SPERO, DM ;
YOON, SK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (08) :3162-3164
[6]  
ALPERT L, 1997, P AM ASS CANC RES, V38
[7]   Total synthesis of (-)-hemiasterlin, a structurally novel tripeptide that exhibits potent cytotoxic activity [J].
Andersen, RJ ;
Coleman, JE ;
Piers, E ;
Wallace, DJ .
TETRAHEDRON LETTERS, 1997, 38 (03) :317-320
[8]  
Anderson HJ, 1997, CANCER CHEMOTH PHARM, V39, P223
[9]  
BAI R, 1991, J BIOL CHEM, V266, P15882
[10]  
BAI R, 1990, J BIOL CHEM, V265, P17141