Natural products from Peperomia: occurrence, biogenesis and bioactivity

被引:0
作者
Yasmin Valero Gutierrez
Lydia F. Yamaguchi
Marcilio M. de Moraes
Christopher S. Jeffrey
Massuo J. Kato
机构
[1] University of São Paulo,Research Support Center in Molecular Diversity of Natural Products, Institute of Chemistry
[2] University of Nevada,Department of Chemistry
来源
Phytochemistry Reviews | 2016年 / 15卷
关键词
Piperaceae; Secondary metabolites;
D O I
暂无
中图分类号
学科分类号
摘要
The Peperomia is one of the giant genus among Angiosperms with approximately 1600 species spread in the tropics. Their species are valuable as ornamental and several medicinal uses were described but their phytochemistry is poorly investigated compared to Piper (2000 species). In spite of this scarcity, typical classes of secondary metabolites isolated from their species are characterized as polyketides, meroterpenes, chromenes, phenylpropanoids, lignans and amides, among which 2-acylcyclohexane-1,3-diones, orsellinic acid-based meroterpenes and secolignans (peperomins) are very specific to Peperomia. The bioactivities of several compounds indicated their potential as antiparasites, antimicrobial, antiviral, cytotoxic agents against several tumoral strains and also as herbicides.
引用
收藏
页码:1009 / 1033
页数:24
相关论文
共 390 条
[1]  
Aqil M(1993)A new flavonol glycoside from Sci Phys Sci 6 141-143
[2]  
Rahman FA(2002)Anti-inflammatory and analgesic activity of J Ethnopharmacol 91 215-218
[3]  
Ahmad MB(2001) (L.) HBK (Piperaceae) Fitoterapia 72 57-58
[4]  
Arrigoni-Blank MDF(1987)Analgesic activity of Phytochemistry 26 2033-2036
[5]  
Dmitrieva EG(2006) aerial parts in mice J Pharm Pharmacol 58 1559-1570
[6]  
Franzotti EM(1975)Lignans from Phytochemistry 14 265-269
[7]  
Aziba PI(2009)Phytochemicals from Chirality 21 799-801
[8]  
Adedeji A(2010) Linn. and their pharmacological properties: a review Tetrahedron Asymmetr 21 2402-2407
[9]  
Ekor M(2011)Xanthones and 4-phenylcoumarins of J Org Chem 76 2603-2612
[10]  
Badheka LP(2012)Resolution and absolute configuration assignment of a natural racemic chromane from Tetrahedron Lett 53 6051-6054