Modern methods to produce natural-product libraries

被引:92
作者
Abel, U [1 ]
Koch, C [1 ]
Speitling, M [1 ]
Hansske, FG [1 ]
机构
[1] BioLeads GmbH, D-69123 Heidelberg, Germany
关键词
D O I
10.1016/S1367-5931(02)00338-1
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
Natural sources offer a wealth of chemically diverse compounds that have been evolutionary preselected to modulate biochemical pathways. Several industrial and academic groups are accessing this source using advanced technology platforms. Methods have been reported to generate large and diverse natural-product libraries optimised for high-throughput screening and for a fast discovery process. In addition to prefractionated and pure natural-product libraries, parallel synthesis gives access to synthetic, semi-synthetic and natural-product-like libraries. Natural-product chemistry and organic synthesis are powerful tools for optimising natural leads and for generating new diversity from natural scaffolds. The amalgamation of both may be expected to become an important strategy in future drug design.
引用
收藏
页码:453 / 458
页数:6
相关论文
共 65 条
[1]   Combinatorial modification of natural products: Preparation of unencoded and encoded libraries of Rauwolfia alkaloids [J].
Atuegbu, A ;
Maclean, D ;
Nguyen, C ;
Gordon, EM ;
Jacobs, JW .
BIOORGANIC & MEDICINAL CHEMISTRY, 1996, 4 (07) :1097-1106
[2]   Pure compound libraries; a new perspective for natural product based drug discovery [J].
Bindseil, KU ;
Jakupovic, J ;
Wolf, D ;
Lavayre, J ;
Leboul, J ;
van der Pyl, D .
DRUG DISCOVERY TODAY, 2001, 6 (16) :840-847
[3]  
Brohm D, 2002, ANGEW CHEM INT EDIT, V41, P307, DOI 10.1002/1521-3773(20020118)41:2<307::AID-ANIE307>3.0.CO
[4]  
2-1
[5]   Total synthesis of naturally occurring prostaglandin F2α on a non-cross-linked polystyrene support [J].
Chen, SQ ;
Janda, KD .
TETRAHEDRON LETTERS, 1998, 39 (23) :3943-3946
[6]   Synthesis of prostaglandin E-2 methyl ester on a soluble-polymer support for the construction of prostanoid libraries [J].
Chen, SQ ;
Janda, KD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (37) :8724-8725
[7]   The synthesis of a combinatorial library using a tambjamine natural product template [J].
Davis, RA ;
Carroll, AR ;
Quinn, RJ .
AUSTRALIAN JOURNAL OF CHEMISTRY, 2001, 54 (06) :355-359
[8]   Solution phase synthesis of libraries of polycyclic natural product analogue by cascade radical annulation: Synthesis of a 64-member library of mappicine analogues and a 48-member library of mappicine ketone analogues [J].
de Frutos, O ;
Curran, DP .
JOURNAL OF COMBINATORIAL CHEMISTRY, 2000, 2 (06) :639-649
[9]   An efficient solid-phase synthesis of the vitamin D3 system [J].
Doi, T ;
Hijikuro, I ;
Takahashi, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (28) :6749-6750
[10]   Comprehensive survey of combinatorial library synthesis: 2000 [J].
Dolle, RE .
JOURNAL OF COMBINATORIAL CHEMISTRY, 2001, 3 (06) :477-517