Biased photo cleavage of N-/N-nitrobenzyl from 2’-hydroxyethyl-adenosine and their DNA/RNA Caged-analogues

Author(s):  
Amarnath Bollu ◽  
Nagendra K. Sharma
Keyword(s):  
2008 ◽  
Vol 7 (2) ◽  
pp. 97-107 ◽  
Author(s):  
M. C. Prabhakara ◽  
H. S. Bhojya Naik

2013 ◽  
Vol 23 (5) ◽  
pp. 897-908 ◽  
Author(s):  
A. Srishailam ◽  
Yata Praveen Kumar ◽  
Nazar M. D. Gabra ◽  
P. Venkat Reddy ◽  
N. Deepika ◽  
...  

2010 ◽  
Vol 8 (1) ◽  
pp. 96-107 ◽  
Author(s):  
Natarajan Raman ◽  
Arumugam Sakthivel ◽  
Ramaraj Jeyamurugan

AbstractFew novel binuclear Schiff base metal complexes [M2LCl3], where M = Cu(II) and Zn(II); L= 2,6-bis-({2-[(3-hydroxy-4-nitrobenzylidene)amino]ethylimino}methyl)-4-methylphenol (BHEM), 2,6-bis-({2-[(3,4-dimethoxybenzylidene)amino]ethylimino} methyl)-4-methylphenol (BDEM) and 2,6-bis-({2-[(2,3,5-trichlorobenzylidene)amino]ethylimino}methyl)-4-methylphenol (BTEM), have been synthesized and characterized by analytical and spectral data. The data suggest that BHEM/BDEM/BTEM ligands afford square-pyramidal/distorted square-pyramidal geometry on metalation with Zn(II)/Cu(II). The binding behaviour of these complexes with DNA has been investigated using electronic absorption spectroscopy as well as viscosity and voltammetric measurements; the results show that they interact with DNA through intercalating way. From the DNA cleavage study of these complexes, investigated by gel electrophoresis, we found that they efficiently cleave supercoiled pUC19 DNA in the presence of a reducing agent (3-mercaptopropionic acid) and on irradiation with UV light of 360 nm wavelength. The mechanism reveals that singlet oxygen (1O2) plays a significant role in the photo cleavage. The superoxide dismutase (SOD) mimetic activity of the synthesized complexes demonstrates that most of the complexes have promising SOD-mimetic activity. The antimicrobial study indicates that the complexes inhibit the growth of bacteria and fungi more than the free ligands.


Author(s):  
Vega Widya Karisma ◽  
Wei Wu ◽  
Mingxing Lei ◽  
Huawen Liu ◽  
Muhammad Farrukh Nisar ◽  
...  

Light has attracted special attention as a stimulus for triggered drug delivery systems (DDS) due to its intrinsic features of being spatially and temporally tunable. Ultraviolet A (UVA) radiation has recently been used as a source of external light stimuli to control the release of drugs using a “switch on- switch off” procedure. This review discusses the promising potential of UVA radiation as the light source of choice for photo-controlled drug release from a range of photo-responsive and photolabile nanostructures via photo-isomerization, photo-cleavage, photo-crosslinking, and photo-induced rearrangement. In addition to its clinical use, we will also provide here an overview of the recent UVA-responsive drug release approaches that are developed for phototherapy and skin photoprotection.


2016 ◽  
Vol 3 (6) ◽  
pp. 861-865 ◽  
Author(s):  
Xu Liu ◽  
Zikuan Wang ◽  
Xianyuan Zhao ◽  
Xuefeng Fu
Keyword(s):  

Photocatalytic hydrodefluorination of a series of perfluoroarenes by rhodium porphyrin complexes was described. The key intermediate (por)Rh-C6F4R underwent fast photo-cleavage of Rh–C bonds to produce hydrodefluorination products.


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