Covering: 1999 to August 2009. Previous review: Nat. Prod. Rep., 2000, 17, 117 In the review period, 97 new representatives of Stemona alkaloids were described, bringing the total reported so far to 139. In this review, we discuss their isolation, structural elucidation, structural classification, biological activities, semi-synthesis and total syntheses. These alkaloids are classified into seven groups displaying either a pyrrolo[1,2-a]azepine or a pyrido[1,2-a]azepine core, and a miscellaneous group comprising those alkaloids without these structural motifs, together with those that are the sole representative of a new group.
Nature is an inexhaustible source of natural compounds with interesting biological activities. Ingeneral, natural products are an important source of new compounds with a variety of structural arrangementsand singular properties. Styryl lactones are a group of secondary metabolites ubiquitous in the genusGoniothalamus that have demonstrated to possess interesting biological properties, in particularantiproliferative activity against cancer cells. In general, the cytotoxicity of styryl lactones appears to bespecific against cancer cells since insignificant effects of these compounds on normal cells are reported. Alarge body of evidence suggests that the antiproliferative activity of styryl lactones is associated with theinduction of apoptosis in target cells. In the first part of this review we discuss the biological activities ofstyryl lactones focusing on cancer cells, the causal agent of Chagas disease and the vectors for yellow feverand human lymphatic filariasis. Structure-activity relationship s are described in detail for ninety styryllactones. The last part describes the molecular targets of styryl lactones for inducing apoptosis, as well asimmunosuppressive and inflammatory processes. Overall, understanding how these compounds exert theiractivities in biological system is essential for future development and application of styryl lactones forhuman health.
1 February 2006 in Bioorganic & Medicinal Chemistry