Synthesis, Biological Activity and Action Mechanism Study of Novel Chalcone Derivatives Containing Malonate

2020 ◽  
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Author(s):  
Tao Guo ◽  
Rongjiao Xia ◽  
Tingting Liu ◽  
Feng Peng ◽  
Xuemei Tang ◽  
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RSC Advances ◽  
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pp. 24942-24950 ◽  
Author(s):  
Tao Guo ◽  
Rongjiao Xia ◽  
Mei Chen ◽  
Jun He ◽  
Shijun Su ◽  
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Synthesis, antibacterial, antiviral activities and action mechanism of chalcone derivatives containing thiophene sulfonate.


2004 ◽  
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Author(s):  
WEI DING ◽  
ZHIMO ZHAO ◽  
WENJUN WU ◽  
HUIYING TAO ◽  
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Wenke Miao ◽  
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Shanshan Wu ◽  
Xue Qin ◽  
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Vol 78 (2) ◽  
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Author(s):  
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Fatma Kaynak-Onurdag ◽  
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Selda Özgen Özgacar

2019 ◽  
Vol 19 (12) ◽  
pp. 1051-1058 ◽  
Author(s):  
Ting Wang ◽  
Zhuyu Xu ◽  
Yongping Lu ◽  
Jianyou Shi ◽  
Wenbo Liu ◽  
...  

Sirtuins family is a class of NDA+ dependent protein deacetylases that play a key role in the regulation of several aspects of biological processes, such as cell cycle regulation, autophagy, immune and inflammatory response. Many studies have shown that sirtuins2 as a key player in the cancer pathway is of great significance in tumorigenesis. This review summarizes the newly discovered, in recent years, some SIRT2 inhibitors for cancer target structure, action mechanism, biological activity, substrate specificity, and signaling pathways.


Biota ◽  
2020 ◽  
Vol 13 (1) ◽  
Author(s):  
Novia Suryani ◽  
Sabirin Matsjeh ◽  
Mutmainah Mutmainah ◽  
Daratu Eviana Kusuma Putri Eviana Kusuma Putri ◽  
Damayanti Iskandar ◽  
...  

Chalcone is one of the phenolic group secondary metabolic with numerous biological activity. Many studies have shown that chalcone derivatives compound has anticancer, anti-inflammatory, antimalarial, and antibacterial activities. The purpose of this research was to study the prediction potency unsaturated carbonyl system of chalcone derivative against the HeLa cell by MTT assay. Those activities assumed can inhibit the mechanism action of NF-kB that caused cervical cancer. The 2,4-dihydroxide-4’-methoxychalcone has done synthesis as a target compound by a sonochemical for 7 hours. The results showed that chalcone derivative most active against the HeLa cell.  


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