Aromatic C-nitrosation by a copper(ii)–nitrosyl complex

2015 ◽  
Vol 44 (4) ◽  
pp. 1829-1835 ◽  
Author(s):  
Kanhu Charan Rout ◽  
Biplab Mondal

Addition of nitric oxide to the methanol solution of copper(ii) complex of 4-amino-3-hydroxy-1-sulphonic acid, resulted in the reduction of Cu(ii) center through unstable copper(ii)-nitrosyl intermediate. The reduction was accompanied with simultaneous C-nitrosation of the aromatic ring of the ligand.

2005 ◽  
Vol 358 (10) ◽  
pp. 2891-2899 ◽  
Author(s):  
Henrique E. Toma ◽  
Anamaria D.P. Alexiou ◽  
André Luiz B. Formiga ◽  
Marcelo Nakamura ◽  
Sergio Dovidauskas ◽  
...  

Author(s):  
Niklas Gessner ◽  
Anna Karina Bäck ◽  
Johannes Knorr ◽  
Christoph Nagel ◽  
Philipp Marquetand ◽  
...  

Transition metal complexes capable of releasing small molecules such as carbon monoxide and nitric oxide upon photoactivation are versatile tools in various fields of chemistry and biology. In this work,...


2018 ◽  
Vol 2018 ◽  
pp. 1-15 ◽  
Author(s):  
Fabio Arias ◽  
M. Encarnación Camacho ◽  
M. Dora Carrión ◽  
Meriem Chayah ◽  
Miguel Romero ◽  
...  

Two new families of pyrazoline and thiadiazoline heterocycles have been developed. Their inhibitory activities against two different isoforms of nitric oxide synthase (inducible and neuronal NOS) are reported. The novel derivatives were synthesized combining the arylthiadiazoline or arylpyrazoline skeleton and a carboxamide or carbothioamide moiety, used as starting material ethyl 2-nitrobenzoates or substituted nitrobenzaldehydes, respectively. The structure-activity relationships of final molecules are discussed in terms of the R1 radical effects in the aromatic ring, the Y atom in the heterocyclic system, the X heteroatom in the main chain, and the R2 substituent in the carboxamide or carbothioamide rest. In general, thiadiazolines (5a–e) inhibit preferentially the neuronal isoform; among them, 5a is the best nNOS inhibitor (74.11% at 1 mM, IC50 = 420 μM). In contrast, pyrazolines (6a–r) behave better as iNOS than nNOS inhibitors, 6m being the best molecule of this series (76.86% at 1 mM of iNOS inhibition, IC50 = 130 μM) and the most potent of all tested compounds.


1995 ◽  
Vol 270 (39) ◽  
pp. 22997-23006 ◽  
Author(s):  
Husam M. Abu-Soud ◽  
Jianling Wang ◽  
Denis L. Rousseau ◽  
Jon M. Fukuto ◽  
Louis J. Ignarro ◽  
...  

Gut ◽  
1999 ◽  
Vol 45 (6) ◽  
pp. 864-873 ◽  
Author(s):  
D-M McCafferty ◽  
M Miampamba ◽  
E Sihota ◽  
K A Sharkey ◽  
P Kubes

2005 ◽  
Vol 127 (40) ◽  
pp. 13758-13759 ◽  
Author(s):  
Raju Prakash ◽  
Alexander U. Czaja ◽  
Frank W. Heinemann ◽  
Dieter Sellmann

2008 ◽  
Vol 5 (3) ◽  
pp. 389-398 ◽  
Author(s):  
Qingdong Zheng ◽  
Adela Bonoiu ◽  
Tymish Y. Ohulchanskyy ◽  
Guang S. He ◽  
Paras N. Prasad

2008 ◽  
Vol 457 (2) ◽  
pp. 271-279 ◽  
Author(s):  
Karol Ondrias ◽  
Andrej Stasko ◽  
Sona Cacanyiova ◽  
Zdena Sulova ◽  
Olga Krizanova ◽  
...  

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