Tetraethylene Glycol Tethered Heteronuclear Bis-isatin Derivatives: Design, Synthesis, and In Vitro Anti-mycobacterial Activities

2018 ◽  
Vol 55 (9) ◽  
pp. 2172-2177 ◽  
Author(s):  
Shuang-Qi Zhao ◽  
Yan Xu ◽  
Jianguo Guan ◽  
Shijia Zhao ◽  
Guang-De Zhang ◽  
...  
2018 ◽  
Vol 55 (12) ◽  
pp. 3006-3010 ◽  
Author(s):  
Shi‐Jia Zhao ◽  
Zao‐Sheng Lv ◽  
Jia‐Lun Deng ◽  
Feng Gao ◽  
Guang‐De Zhang ◽  
...  

Fitoterapia ◽  
2018 ◽  
Vol 127 ◽  
pp. 383-386 ◽  
Author(s):  
Yan Xu ◽  
Jianguo Guan ◽  
Zhi Xu ◽  
Shijia Zhao

2014 ◽  
Vol 24 (2) ◽  
pp. 591-594 ◽  
Author(s):  
Kailin Han ◽  
Yao Zhou ◽  
Fengxi Liu ◽  
Qiannan Guo ◽  
Pengfei Wang ◽  
...  

2018 ◽  
Vol 55 (12) ◽  
pp. 2985-2989 ◽  
Author(s):  
Shi‐Jia Zhao ◽  
Zao‐Sheng Lv ◽  
Lin Shi ◽  
Shuang‐Qi Zhao ◽  
Zhi Xu

2021 ◽  
Vol 12 (2) ◽  
pp. 2392-2403

A series of novel benzoxazole-isatin conjugates were synthesized by treating 2-amino benzoxazole with 5 and 7 substituted isatin derivatives and were screened for in vitro antimicrobial and cytotoxic activities. The results showed that all the synthesized compounds shown mild to potent antibacterial activity. The MIC values were found between 10 and 100 µg/ml against tested bacterial and fungal organisms. Among all the compounds, 3d & 3c showed good antimicrobial. In vitro cytotoxic activities were evaluated by MTT assay of all the test compounds against the different human cancer cell lines. The compounds having substitution with electron-withdrawing groups (halides) at the 5th position on the isatin ring showed the most significant biological activity than substituted at the 7th position. The molecular docking interactions have shown good binding interactions with the protein targets glucosamine-6-phosphate synthase (GlcN-6-P synthase) and telomerase.


2005 ◽  
Vol 13 (9) ◽  
pp. 3249-3261 ◽  
Author(s):  
Idan Chiyanzu ◽  
Cailean Clarkson ◽  
Peter J. Smith ◽  
Julie Lehman ◽  
Jiri Gut ◽  
...  

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