ChemInform Abstract: Quassinoids: Structural Diversity, Biological Activity and Synthetic Studies

ChemInform ◽  
2008 ◽  
Vol 39 (30) ◽  
Author(s):  
Ivo J. Curcino Vieira ◽  
Raimundo Braz-Filho
2021 ◽  
Vol 192 ◽  
pp. 112927
Author(s):  
Hong-Zhen Shu ◽  
Cheng Peng ◽  
Lan Bu ◽  
Li Guo ◽  
Fei Liu ◽  
...  

Biochemistry ◽  
2010 ◽  
Vol 49 (8) ◽  
pp. 1798-1807 ◽  
Author(s):  
Hidekazu Katayama ◽  
Hironobu Hojo ◽  
Tsuyoshi Ohira ◽  
Akira Ishii ◽  
Takamichi Nozaki ◽  
...  

2008 ◽  
Vol 3 (2) ◽  
pp. 438-446 ◽  
Author(s):  
Kenichiro Shimokawa ◽  
Itsuka Mashima ◽  
Akiko Asai ◽  
Tomohiro Ohno ◽  
Kaoru Yamada ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5386
Author(s):  
Shean-Yeaw Ng ◽  
Chin-Soon Phan ◽  
Takahiro Ishii ◽  
Takashi Kamada ◽  
Toshiyuki Hamada ◽  
...  

Members of the marine soft coral genus Xenia are rich in a diversity of diterpenes. A total of 199 terpenes consisting of 14 sesquiterpenes, 180 diterpenes, and 5 steroids have been reported to date. Xenicane diterpenes were reported to be the most common chemical skeleton biosynthesized by members of this genus. Most of the literature reported the chemical diversity of Xenia collected from the coral reefs in the South China Sea and the coastal waters of Taiwan. Although there was a brief review on the terpenoids of Xenia in 2015, the present review is a comprehensive overview of the structural diversity of secondary metabolites isolated from soft coral genus Xenia and their potent biological activity as reported between 1977 to 2019.


2016 ◽  
Vol 33 (11) ◽  
pp. 1318-1343 ◽  
Author(s):  
Zhong Jin

The latest progress on the isolation, identification, biological activity and synthetic studies of the structurally diverse alkaloids from plants of family Amaryllidaceae has been summarized in this review.


ChemInform ◽  
2009 ◽  
Vol 40 (39) ◽  
Author(s):  
Sandrine Gerber-Lemaire ◽  
Pierre Vogel

Author(s):  
Wang Wang ◽  
Yueying Yang ◽  
Yang Liu ◽  
Dejuan Sun ◽  
Hua Li ◽  
...  

: Natural products have remarkable structural diversity and biological characteristics, providing researchers with more possibilities to develop novel drugs for disease therapeutics. Andrographolide, an ent-labdane diterpenoid from traditional Chinese medicines, Andrographis paniculata, exhibits a broad range of biological activities, which has been a hot area of research for several years. Up to now, lots of its derivatives with multiple bioactivities have been prepared through chemical modification. This review summarizes andrographolide derivatives prepared in the last ten years (2006-present), classifies them by different biological activities, and provides some discussion about the design of novel and potent derivatives.


2015 ◽  
Vol 32 (6) ◽  
pp. 811-840 ◽  
Author(s):  
Darcy J. Atkinson ◽  
Margaret A. Brimble

The rubromycins are a unique family of natural products. This review covers their isolation, biological activity, biosynthesis and a detailed discussion of the diverse chemistry employed for total synthesis.


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