Pyridazines

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Pyridazine Nucleus: A Pharmacophoric Moiety For Bio-Active Compounds

Journal Title, Volume, Page: 
Aphcao 66,S35-S38.
Year of Publication: 
1996
Authors: 
Naser, A.-Z.
Current Affiliation: 
Department of Pharmacy, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine
Baraldi, P. G.
Cacciari, B.
Pineda de Las Infantas, M. J.
Preferred Abstract (Original): 

The authors describe the substitution of an arom. ring with the pyridazine nucleus in the prepn. of several classes of bio-active compds. The authors described the prepn. of cardiotonics, of DNA minor groove binders such as tallimustine and anthramycin pyridazine analogs, and C-glycosides of pyridazines as antiviral agents. 

warad's picture

Comparative Study of new Pyridazine Derivatives Tow Ards Corrosion of Copper in Nitric Acid: Part-1

Journal Title, Volume, Page: 
Int. J. Electrochem. Sci., 5 (2010) 696 - 705
Year of Publication: 
2010
Authors: 
A. Zarrouk
LCAE-URAC18, Faculté des Sciences, Université Mohammed Ier B.P. 717, 60000 Oujda, Morocco
T. Chelfi
LCAE-URAC18, Faculté des Sciences, Université Mohammed Ier B.P. 717, 60000 Oujda, Morocco
A. Dafali
LCAE-URAC18, Faculté des Sciences, Université Mohammed Ier B.P. 717, 60000 Oujda, Morocco
B. Hammouti
LCAE-URAC18, Faculté des Sciences, Université Mohammed Ier B.P. 717, 60000 Oujda, Morocco
S.S. Al-Deyab
Department of Chemistry - College of Science, King Saud University, B.O. 2455 Riaydh 11451 Saudi Arabia
I. Warad
Department of Chemistry - College of Science, King Saud University, B.O. 2455 Riaydh 11451 Saudi Arabia
Current Affiliation: 
Department of Chemistry, Faculty of Science, An-Najah National University, Nablus, Palestine
N. Benchat
LCAE-URAC18, Faculté des Sciences, Université Mohammed Ier B.P. 717, 60000 Oujda, Morocco
M. Zertoubi
Laboratoire LEMI, Faculté des sciences, Université Ain Chock casablanca, B.P 5366 Maarif Casablanca
Preferred Abstract (Original): 
The inhibition of the corrosion of copper in 2M HNO3 by 5-[hydroxy(phenyl)methyl]-6 methylpyridazin-3 (2.6 )-one (P1), 4-(2-chlorobenzyl)-6-hydrazino-3-methyl-1,6-dihydropyridazine (P2), 5-(2,6-dichlorobenzyl) -6-methylpyridazin-3(2H)-one (P3) and 5-[(2chlorophenyl) (hydroxy)methyl]-6-methylpyridazin-3(2H)-one (P4) has been investigated at 303K using weight loss measurements, potentiodynamic polarisation and electrochemical impedance spectroscopy (EIS) methods). Results obtained show that P3 and P4 are the best inhibitors and their inhibition efficiencies (E %) increase with the increase of inhibitor concentration and reach up to 96 and 94 % for P3 and P4 at 10-3 M, respectively. Moreover, polarisation studies clearly reveal that the presence of inhibitors changes the mechanism of hydrogen evolution and that they act as mixed inhibitors. EIS study shows that charge transfer resistance increases with the inhibitor concentration. The adsorption of P3 obeys to the Langmuir isotherm. The activation parameters of copper in the presence and absence of P3 are also evaluated and discussed. Effect of temperature is studied between 298 and 353 K and determination of activation parameters is also discussed in part 2. Explanation by quantum indices to correlate inhibition efficiency should be given in part 3.
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