High Phenoxazinone Synthase Activity of Two Mononuclear cis-Dichloro Cobalt(II) Complexes with Rigid Pyridyl Scaffold

2021 ◽  
Author(s):  
Arabinda Muley ◽  
Kalai Selvan Karumban ◽  
Sadananda Kumbhakar ◽  
Bishnubasu Giri ◽  
Somnath Maji

Phenoxazinone synthase (PHS) is a pentanuclear copper enzyme studied for the last two decades, and though both manganese and copper complexes have been explored extensively, there are only a handful...

2017 ◽  
Vol 46 (4) ◽  
pp. 1249-1259 ◽  
Author(s):  
Shipra Sagar ◽  
Swaraj Sengupta ◽  
Antonio J. Mota ◽  
Shyamal K. Chattopadhyay ◽  
Arturo Espinosa Ferao ◽  
...  

Two tetranuclear copper complexes with a Cu4O4 cubane core exhibiting phenoxazinone synthase like activity are reported.


2017 ◽  
Vol 2 (34) ◽  
pp. 11040-11047 ◽  
Author(s):  
Mamoni Garai ◽  
Dhananjay Dey ◽  
Hare Ram Yadav ◽  
Angshuman Roy Choudhury ◽  
Milan Maji ◽  
...  

1997 ◽  
Vol 94 ◽  
pp. 1695-1714 ◽  
Author(s):  
P Lesot ◽  
F Perez ◽  
P Judeinstein ◽  
JP Bayle ◽  
H Allouchi ◽  
...  

2019 ◽  
Author(s):  
Swaraj Sengupta ◽  
Sahanwaj Khan ◽  
Shyamal K. Chattopadhyay ◽  
Indrani Banerjee ◽  
Tarun K. Panda ◽  
...  

Synthesis and characterisation of one trinuclear copper complex, ([Cu<sub>3</sub>L<sub>3</sub>O]ClO<sub>4</sub>) (<b>1</b>) and one nickel complex ([Ni(L'H)<sub>2</sub>(dmso)<sub>2</sub>](ClO<sub>4</sub>)<sub>2</sub>) (<b>2</b>) with Schiff base ligands: (3Z)-3-((Z)-(1-(thiophen-2-yl)ethylidene)hydrazono)butan-2-one oxime (LH) and 1-(pyridin-2-yl)ethylidene)hydrazono)butan-2-one oxime (L<sup>'</sup>H). <b>1</b> shows high catecholase activity and has also been tested as a catalyst for the synthesis of benzylimine. <b>2 </b> shows phenoxazinone synthase activity.


2019 ◽  
Author(s):  
Chem Int

A series of novel 1, 3, 4-oxadiazole analogues was synthesized from cyclization of hydrazones of substituted 1-ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carbohydrazides were prepared from nalidixic acid. The structures of synthesized oxadiazole derivatives and their copper complexes were elucidated on the basis of FTIR, elemental analyses, 1H-NMR and atomic absorption spectral analysis. It was observed from spectral data that metal ligand ratio was 1:1 in all copper complexes and they were bidentate, coordination was found to be done through oxygen of 4-oxo group and nitrogen of oxadiazole ring. The synthesized compounds were further evaluated with biological activities and compared with parent hydrazones. Copper complexes possess antibacterial and antifungal activities better than the oxadiazoles while they have better antioxidant activity then copper complexes. Parent hydrazones were better in all biological activities than synthesized oxadiazoles.


2019 ◽  
Vol 70 (10) ◽  
pp. 3603-3610
Author(s):  
Madalina Mihalache ◽  
Cornelia Guran ◽  
Aurelia Meghea ◽  
Vasile Bercu ◽  
Ludmila Motelica ◽  
...  

The three copper complexes having a-ketoglutaric acid (H2A) and 1- (o-tolyl) biguanide (TB) ligands have been synthesized and characterized. The proposed formulas for these complexes are: [Cu(TB)(HA)]Cl (C1), [Cu(TB)(HA)CH3COO]�H2O (C2) and [Cu(TB)(HA)](NO3) (C3) where HA represents deprotonated H2A. The complexes obtained were tested for antibacterial activity against Staphylococcus aureus ATCC 25923 and Pseudomonas aeruginosa ATCC 27853, antifungal activity on Candida albicans ATCC 10231 and antitumor activity on HeLa tumor cells. Due to the antitumor, antifungal, antimicrobial activity and inhibition of inert substrate adhesion, complexes synthesized could be used for potential therapeutic applications.


Polyhedron ◽  
2006 ◽  
Vol 25 (13) ◽  
pp. 2559-2564 ◽  
Author(s):  
Martin Breza ◽  
Jozef Kožíšek

2014 ◽  
Vol 136 (17) ◽  
pp. 6235-6238 ◽  
Author(s):  
David S. Weinberger ◽  
Nurul Amin SK ◽  
Kartik Chandra Mondal ◽  
Mohand Melaimi ◽  
Guy Bertrand ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Alexander B. Weberg ◽  
Samuel P. McCollom ◽  
Laura M. Thierer ◽  
Michael R. Gau ◽  
Patrick J. Carroll ◽  
...  

Secondary coordination sphere electrostatic effects tune the valence manifolds of copper centers, impacting molecular geometries, photophysical properties, and redox potentials.


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