Guided by Evolution: Biology-Oriented Synthesis of Bioactive Compound Classes

被引:20
作者
Karageorgis, George [1 ,2 ]
Waldmann, Herbert [1 ]
机构
[1] Max Planck Inst Mol Physiol, Dept Chem Biol, Otto Hahn Str 11, D-44227 Dortmund, Germany
[2] Univ Leeds, Sch Chem, Woodhouse Lane, Leeds LS2 9JT, W Yorkshire, England
来源
SYNTHESIS-STUTTGART | 2019年 / 51卷 / 01期
关键词
natural products; bioorganic chemistry; stereoselective synthesis; high-throughput screening; combinatorial chemistry; NATURAL-PRODUCTS; CHEMICAL SPACE; SCAFFOLD DIVERSITY; RING-DISTORTION; COMPLEX; FRAGMENTS; DISCOVERY; ALKALOIDS; DRUGS; CYCLIZATIONS;
D O I
10.1055/s-0037-1610368
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Biology-oriented-synthesis (BIOS), is a chemocentric approach to identifying structurally novel molecules as tools for chemical biology and medicinal chemistry research. The vast chemical space cannot be exhaustively covered by synthetic chemistry. Thus, methods which reveal biologically relevant portions of chemical space are of high value. Guided by structural conservation in the evolution of both proteins and natural products, BIOS classifies bioactive compound classes in a hierarchical manner based on molecular architecture and bioactivity. Biologically relevant scaffolds inspire and guide the synthesis of BIOS libraries, which calls for the development of suitable synthetic methodologies. These compound collections have enriched biological relevance, leading to the discovery of bioactive small molecules. These potent and selective modulators allow the study of complex biological pathways and may serve as starting points for drug discovery programs. Thus, BIOS can also be regarded as a hypothesis-generating tool, guiding the design and preparation of novel, bioactive molecular scaffolds. This review elaborates the principles of BIOS and highlights selected examples of their application, which have in turn created future opportunities for the expansion of BIOS and its combination with fragment-based compound discovery for the identification of biologically relevant small molecules with unprecedented molecular scaffolds.
引用
收藏
页码:55 / 66
页数:12
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