Design, synthesis and pharmacological evaluation of omeprazole-like agents with anti-inflammatory activity

2013 ◽  
Vol 21 (7) ◽  
pp. 1661-1670 ◽  
Author(s):  
Ahmed O.H. El-Nezhawy ◽  
Ayman R. Biuomy ◽  
Fatma S. Hassan ◽  
Ayman K. Ismaiel ◽  
Hany A. Omar
2012 ◽  
Vol 60 (10) ◽  
pp. 1290-1300 ◽  
Author(s):  
Amal Abdel Haleem Mohamed Eissa ◽  
Gamal Abd El-Hakeem Soliman ◽  
Moayad Hussein Khataibeh

2018 ◽  
Vol 2018 ◽  
pp. 1-11
Author(s):  
Musab Mohamed Ibrahim ◽  
Tilal Elsaman ◽  
Mosab Yahya Al-Nour

The design, synthesis, and development of novel non-steroidal anti-inflammatory drugs (NSAIDs) with better activity and lower side effects are respectable area of research. Novel Diclofenac Schiff’s bases (M1, M2, M4, M7, and M8) were designed and synthesized, and their respective chemical structures were deduced using various spectral tools (IR, 1H NMR, 13C NMR, and MS). The compounds were synthesized via Schiff’s condensation reaction and their anti-inflammatory activity was investigated applying the Carrageenan-induced paw edema model against Diclofenac as positive control. Percentage inhibition of edema indicated that all compounds were exhibiting a comparable anti-inflammatory activity as Diclofenac. Moreover, the anti-inflammatory activity was supported via virtual screening using molecular docking study. Interestingly compound M2 showed the highest in vivo activity (61.32% inhibition) when compared to standard Diclofenac (51.36% inhibition) as well as the best binding energy score (-10.765) and the virtual screening docking score (-12.142).


2017 ◽  
Vol 10 (4) ◽  
pp. 458-464 ◽  
Author(s):  
Rajesh A. Rane ◽  
Mukesh Nandave ◽  
Suresh Nayak ◽  
Anushri Naik ◽  
Dhwani Shah ◽  
...  

2016 ◽  
Vol 791 ◽  
pp. 195-204 ◽  
Author(s):  
Amanda F. Cidade ◽  
Patrícia A. Vasconcelos ◽  
Daiany P.B. Silva ◽  
Iziara F. Florentino ◽  
Géssica A. Vasconcelos ◽  
...  

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