posted on 2014-02-21, 00:00authored byMing Zhao, Tanja Gödecke, Jordan Gunn, Jin-Ao Duan, Chun-Tao Che
Protostane triterpenes belong to a group of tetracyclic triterpene that exhibit
unique structural characteristics. Their natural distribution is primarily limited to the genus
Alisma of the Alismataceae family, but they have also been occasionally found in other
plant genera such as Lobelia, Garcinia, and Leucas. To date, there are 59 known
protostane structures. Many of them have been reported to possess biological properties
such as improving lipotropism, hepatoprotection, anti-viral activity against hepatitis B and
HIV-I virus, anti-cancer activity, as well as reversal of multidrug resistance in cancer cells.
On the other hand, fusidanes are fungal products characterized by 29-nor protostane
structures. They possess antibiotic properties against staphylococci, including the
methicillin-resistant Staphylococcus aureus (MRSA). Fusidic acid is a representative
member which has found clinical applications. This review covers plant sources of the
protostanes, their structure elucidation, characteristic structural and spectral properties, as
well as biological activities. The fungal sources, structural features, biological activities of
fusidanes are also covered in this review. Additionally, the biogenesis of these two types of
triterpenes is discussed and a refined pathway is proposed.