Simple coumarins and analogues in medicinal chemistry: Occurrence, synthesis and biological activity

被引:866
作者
Borges, F
Roleira, F
Milhazes, N
Santana, L
Uriarte, E
机构
[1] Univ Porto, Fac Farm, Unidade Quim Fis Mol, Lab Quim Organ, P-4050047 Oporto, Portugal
[2] Univ Coimbra, Fac Farm, Quim Farmaceut Lab, CEF, P-3000295 Coimbra, Portugal
[3] Univ Santiago, Fac Farm, Dept Quim Organ, Santiago De Compostela 15782, Spain
[4] Inst Super Ciencias Saude Norte, P-4580 Paredes, Portugal
关键词
simple coumarins; occurrence; synthesis; biological activity; SAR and QSAR; separation and identification;
D O I
10.2174/0929867053507315
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
Coumarins, also known as benzopyrones, are present in remarkable amounts in plants, although their presence has also been detected in microorganisms and animal sources. The structural diversity found in this family of compounds led to the division into different categories, from simple coumarins to many other kinds of policyclic coumarins, such as furocoumarins and pyranocoumarins. Simple coumarins and analogues are a large class of compounds that have attracted their interest for a long time due to their biological activities: they have shown to be useful as antitumoural, anti-HIV agents and as CNS-active compounds. Furthermore, they have been reported to have multiple biological activities (anticoagulant, anti-inflammatory), although all these properties have not been evaluated systematically. In addition, their enzyme inhibition properties, antimicrobial and antioxidant activities are other foremost topics of this field of research. The present work is to survey the information published or abstracted from 1990 till 2003, which is mainly related to the occurrence, synthesis and biological importance of simple coumarins and some analogues, such as biscoumarins and triscoumarins. Data are also highlighted, concerning the development of new synthetic strategies that could help in drug design and in the work on SAR or QSAR.
引用
收藏
页码:887 / 916
页数:30
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