scholarly journals Natural and Synthetic Saponins as Vaccine Adjuvants

Vaccines ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 222
Author(s):  
Pengfei Wang

Saponin adjuvants have been extensively studied for their use in veterinary and human vaccines. Among them, QS-21 stands out owing to its unique profile of immunostimulating activity, inducing a balanced Th1/Th2 immunity, which is valuable to a broad scope of applications in combating various microbial pathogens, cancers, and other diseases. It has recently been approved for use in human vaccines as a key component of combination adjuvants, e.g., AS01b in Shingrix® for herpes zoster. Despite its usefulness in research and clinic, the cellular and molecular mechanisms of QS-21 and other saponin adjuvants are poorly understood. Extensive efforts have been devoted to studies for understanding the mechanisms of QS-21 in different formulations and in different combinations with other adjuvants, and to medicinal chemistry studies for gaining mechanistic insights and development of practical alternatives to QS-21 that can circumvent its inherent drawbacks. In this review, we briefly summarize the current understandings of the mechanism underlying QS-21’s adjuvanticity and the encouraging results from recent structure-activity-relationship (SAR) studies.

RSC Advances ◽  
2021 ◽  
Vol 11 (20) ◽  
pp. 12254-12287
Author(s):  
Faheem ◽  
Banoth Karan Kumar ◽  
Kondapalli Venkata Gowri Chandra Sekhar ◽  
Subhash Chander ◽  
Selvaraj Kunjiappan ◽  
...  

This review provides critical insights into the biological activities and Structure–Activity Relationship (SAR) studies of tetrahydroisoquinoline (THIQ) analogs.


2016 ◽  
Vol 111 ◽  
pp. 138-159 ◽  
Author(s):  
Andrea Nuzzi ◽  
Annalisa Fiasella ◽  
Jose Antonio Ortega ◽  
Chiara Pagliuca ◽  
Stefano Ponzano ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (24) ◽  
pp. 5847
Author(s):  
Satheesh Gujarathi ◽  
Maroof Khan Zafar ◽  
Xingui Liu ◽  
Robert L. Eoff ◽  
Guangrong Zheng

Garcinoic acid has been identified as an inhibitor of DNA polymerase β (pol β). However, no structure-activity relationship (SAR) studies of garcinoic acid as a pol β inhibitor have been conducted, in part due to the lack of an efficient synthetic method for this natural product and its analogs. We developed an efficient semi-synthetic method for garcinoic acid and its analogs by starting from natural product δ-tocotrienol. Our preliminary SAR studies provided a valuable insight into future discovery of garcinoic acid-based pol β inhibitors.


2018 ◽  
Vol 16 (42) ◽  
pp. 7833-7842 ◽  
Author(s):  
Yong-Guang Gao ◽  
Xiao Lin ◽  
Kai Dang ◽  
Shan-Feng Jiang ◽  
Ye Tian ◽  
...  

Structure–activity relationship (SAR) studies are very critical to design ideal gene vectors for gene delivery.


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