Total synthesis and biological evaluation of viscolin, a 1,3-diphenylpropane as a novel potent anti-inflammatory agent

2006 ◽  
Vol 16 (24) ◽  
pp. 6155-6160 ◽  
Author(s):  
Chung-Ren Su ◽  
Yuh-Chiang Shen ◽  
Ping-Chung Kuo ◽  
Yann-Lii Leu ◽  
Amooru G. Damu ◽  
...  
2020 ◽  
Vol 18 (30) ◽  
pp. 5906-5917
Author(s):  
Carina Weber ◽  
Nina Vierengel ◽  
Thorsten Walter ◽  
Torsten Behrendt ◽  
Tobias Lucas ◽  
...  

Seven new macrolactones of the oxacyclododecindione family have been synthesized and tested for their inhibitory activity on TGF-β-inducible Smad2/3- as well as IL-4-inducible STAT6-dependent signalling pathways.


2014 ◽  
Vol 744 ◽  
pp. 147-156 ◽  
Author(s):  
Kyun Ha Kim ◽  
Young-Don Park ◽  
Heejin Park ◽  
Keum-Ok Moon ◽  
Ki-Tae Ha ◽  
...  

2019 ◽  
Vol 2019 (13) ◽  
pp. 2376-2381 ◽  
Author(s):  
Hanuman P. Kalmode ◽  
Suhag S. Patil ◽  
Kishor L. Handore ◽  
Paresh R. Athawale ◽  
Rambabu Dandela ◽  
...  

Fitoterapia ◽  
2017 ◽  
Vol 121 ◽  
pp. 212-222 ◽  
Author(s):  
Hai-Wen Ding ◽  
Ai-Ling Huang ◽  
Yi-Long Zhang ◽  
Bo Li ◽  
Chen Huang ◽  
...  

2017 ◽  
Vol 13 (2) ◽  
pp. 186-195 ◽  
Author(s):  
Jelena Savic ◽  
Sanda Dilber ◽  
Marina Milenkovic ◽  
Jelena Kotur-Stevuljevic ◽  
Bojan Markovic ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3224
Author(s):  
Leander Geske ◽  
Ulrich Kauhl ◽  
Mohamed E. M. Saeed ◽  
Anja Schüffler ◽  
Eckhard Thines ◽  
...  

The biological activities of shancigusin C (1) and bletistrin G (2), natural products isolated from orchids, are reported along with their first total syntheses. The total synthesis of shancigusin C (1) was conducted by employing the Perkin reaction to forge the central stilbene core, whereas the synthesis of bletistrin G (2) was achieved by the Wittig olefination followed by several regioselective aromatic substitution reactions. Both syntheses were completed by applying only renewable starting materials according to the principles of xylochemistry. The cytotoxic properties of shancigusin C (1) and bletistrin G (2) against tumor cells suggest suitability as a starting point for further structural variation.


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