A Schiff base platform: structures, sensing of Zn(ii) and PPi in aqueous medium and anticancer activity

2017 ◽  
Vol 46 (29) ◽  
pp. 9498-9510 ◽  
Author(s):  
Barnali Naskar ◽  
Ritwik Modak ◽  
Dilip K. Maiti ◽  
Michael G. B. Drew ◽  
Antonio Bauzá ◽  
...  

A Schiff base platform was explored to present structural aspects of its Zn(ii) and Cd(ii) coordination compounds, sensing behavior towards Zn(ii) and PPi in aqueous medium and anticancer activity.

2019 ◽  
Vol 131 (8) ◽  
Author(s):  
Rajasekaran Dhivya ◽  
Asaithambi Gomathi ◽  
Periasamy Viswanathamurthi

2020 ◽  
Vol 49 (26) ◽  
pp. 8991-9001 ◽  
Author(s):  
Sujaya Chakraborty ◽  
Somenath Lohar ◽  
Koushik Dhara ◽  
Raktim Ghosh ◽  
Somasri Dam ◽  
...  

A new structurally characterised half-condensed Schiff base (HL′) and a Zn2L4 complex reacting from Zn2+ ion and HL produced from HL′ in a solution state as smart chemosensors for Zn2+ and H2PO4− ions respectively in aqueous medium.


2021 ◽  
Author(s):  
Nazanin Kordestani ◽  
Hadi Amiri Rudbari ◽  
Alexandra R Fernandes ◽  
Luís R Raposo ◽  
André Luz ◽  
...  

To investigate the effect of different halogen substituents, leaving groups and the flexibility of ligand on the anticancer activity of copper complexes, sixteen copper(II) complexes with eight different tridentate Schiff-base...


2020 ◽  
Author(s):  
Lifeng Hao ◽  
Cao Feng ◽  
Hua Jiahui ◽  
Wang Jianqiang ◽  
Wang Cheng ◽  
...  

INDIAN DRUGS ◽  
2019 ◽  
Vol 56 (03) ◽  
pp. 12-17
Author(s):  
Manpreet Kaur ◽  
S. Singh ◽  

A new series of 2,5-disubstituted-1,3,4-oxadiazole derivatives has been synthesized with the help of different aromatic benzaldehydes and final compounds were characterized by FTIR and 1H NMR. 2,5- disubstituted-1,3,4-oxadiazole derivatives were synthesized by the reaction of Schiff base derivatives with 2,5-disubstituted-1,3,4-oxadiazoles. All the synthesized compounds were screened for their anticancer activity. These compounds were evaluated for their anticancer activity against various cancer cell lines. Five of the compounds possessed good to moderate anti-cancer activity. Three of the synthesized compounds i.e. 6a, 6f and 6g were found to possess maximum growth inhibition. The order for the % control growth inhibition of MCF-7 was found to be 6a>6f>6g>5b>6h, as shown in Table II-VI.


Sign in / Sign up

Export Citation Format

Share Document