scholarly journals Total Synthesis and Structure-Activity Relationship of Glycoglycerolipids from Marine Organisms

Marine Drugs ◽  
2014 ◽  
Vol 12 (6) ◽  
pp. 3634-3659 ◽  
Author(s):  
Jun Zhang ◽  
Chunxia Li ◽  
Guangli Yu ◽  
Huashi Guan
Keyword(s):  
Total Synthesis ◽  
Structure Activity Relationship ◽  
Marine Organisms ◽  
Activity Relationship ◽  
Structure Activity ◽  
Relationship Of

scholarly journals Concise Total Synthesis of (+)-Zeylenone with Antitumor Activity and Structure-Activity Relationship of Its Derivatives

2019 ◽  
Author(s):  
Zhonghao Sun ◽  
Shuxian Yang ◽  
Chengfang Xu ◽  
Guoxu Ma ◽  
Li Cao ◽  
...  
Keyword(s):  
Antitumor Activity ◽  
Total Synthesis ◽  
Human Cancer ◽  
Synthesis Method ◽  
Structure Activity Relationship ◽  
Single Step ◽  
Activity Relationship ◽  
Human Cancer Cell Lines ◽  
Structure Activity ◽  
Relationship Of

(-)-Zeylenone is a promising cytotoxic agent，which is a natural product isolated from Uvaria grandiflora Roxb. Though substantial antitumor mechanism has been researched , little has focused on its enantiomer (+)-Zeylenone.This article will try to find a gram scale synthesis method of (+)-Zeylenone and explain the structure-activity relationship of this kind of compound. Total synthesis of (+)-zeylenone was completed in 13 steps with quinic acid as starting material in 8.8% overall yield. The highlight of the route was the control of the three carbon’s chirality by clever use of single step dihydroxylation under the direction of the key C-3 chirality. In addition, zeylenone derivatives were designed and synthesized and their antitumor activity were evaluated against three human cancer cell lines using the CCK8 assay. Structure-activity relationship suggested compounds with both two absolute configurations exhibited good activity. Besides, hydroxyls at C-1/2 position were crucial for the activity and esterification of C-1 hydroxyl with large groups made the activity disappeared. Hydroxyl at C-3 position was also important as proper ester substituent could increase the potency.

scholarly journals Improved Total Synthesis and Structure-Activity Relationship of Arenastatin A, a Potent Cytotoxic Spongean Depsipeptide.

1995 ◽  
Vol 43 (9) ◽  
pp. 1598-1600 ◽  
Author(s):  
Motomasa KOBAYASHI ◽  
Weiqi WANG ◽  
Naoki OHYABU ◽  
Michio KUROSU ◽  
Isao KITAGAWA
Keyword(s):  
Total Synthesis ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Structure Activity ◽  
Relationship Of

Total synthesis, chemical modification and structure-activity relationship of bufadienolides

2020 ◽  
Vol 189 ◽  
pp. 112038 ◽  
Author(s):  
Yue- Zhong ◽  
Chao- Zhao ◽  
Wen-Yu Wu ◽  
Tian-Yuan Fan ◽  
Nian-Guang Li ◽  
...  
Keyword(s):  
Chemical Modification ◽  
Total Synthesis ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Structure Activity ◽  
Relationship Of

Structure-activity relationship of (-) mammea A/BB derivatives against Leishmania amazonensis

Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
MA Brenzan ◽  
CV Nakamura ◽  
BPD Filho ◽  
T Ueda-Nakamura ◽  
MCM Young ◽  
...  
Keyword(s):  
Structure Activity Relationship ◽  
Leishmania Amazonensis ◽  
Activity Relationship ◽  
Structure Activity ◽  
Relationship Of
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