Design, synthesis, biological evaluation and in silico studies of novel pyrrolo[3,4-d]pyridazinone derivatives with promising anti-inflammatory and antioxidant activity

2020 ◽  
Vol 102 ◽  
pp. 104035 ◽  
Author(s):  
Łukasz Szczukowski ◽  
Aleksandra Redzicka ◽  
Benita Wiatrak ◽  
Edward Krzyżak ◽  
Aleksandra Marciniak ◽  
...  
2020 ◽  
Vol 186 ◽  
pp. 111863 ◽  
Author(s):  
Muhammad Saeed Jan ◽  
Sajjad Ahmad ◽  
Fida Hussain ◽  
Ashfaq Ahmad ◽  
Fawad Mahmood ◽  
...  

2020 ◽  
Vol 96 ◽  
pp. 103610 ◽  
Author(s):  
Nayera W. Hassan ◽  
Manal N. Saudi ◽  
Yasser S. Abdel-Ghany ◽  
Azza Ismail ◽  
Perihan A. Elzahhar ◽  
...  

2021 ◽  
Vol 106 ◽  
pp. 104476
Author(s):  
Berenika M. Szczęśniak-Sięga ◽  
Benita Wiatrak ◽  
Żaneta Czyżnikowska ◽  
Jan Janczak ◽  
Rafal J. Wiglusz ◽  
...  

2020 ◽  
Vol 105 ◽  
pp. 104386
Author(s):  
Marwa M. Shaaban ◽  
Hanan M. Ragab ◽  
Kenichi Akaji ◽  
Ross P. McGeary ◽  
Alaa-Eldin A. Bekhit ◽  
...  

2021 ◽  
Vol 27 ◽  
Author(s):  
Bharti Rajesh Kumar Shyamlal ◽  
Manas Mathur ◽  
Dharmendra K. Yadav ◽  
Irina V. Mashevskaya ◽  
Mohamed El-Shazly ◽  
...  

Background: Several natural/synthetic molecules having structure similar to 1H-isochromen-1-ones have been reported to display promising antioxidants and platelet aggregation inhibitory activity. Isocoumarin (1H-2-benzopyran-1-one) skeleton, either whole or as a part of molecular framework, have been explored for their antioxidant or antiplatelet activities. Introduction: Based on literature, a new prototype i.e., 3-phenyl-1H-isochromen-1-ones based compounds have been rationalized to possess both antioxidant as well as antiplatelet activities. Consequently, no reports are available regarding its inhibition either by cyclooxygenase-1 (COX-1) enzyme or by arachidonic acid (AA)-induced platelet aggregation. This prompted us to investigate 3-phenyl-1H-isochromen-1-ones towards antioxidant and antiplatelet agents. Methods: The goal of this work to identify new 3-phenyl-1H-isochromen-1-ones based compounds via synthesis of a series of analogues and performing in vitro antioxidant as well as AA-induced antiplatelet activities and then, identification of potent compounds by SAR and molecular docking studies. Results: Out of all synthesized 3-phenyl-1H-isochromen-1-ones analogues, five compounds showed 7-folds to 16-folds highly potent antioxidant activities than ascorbic acid. Altogether, ten 3-phenyl-1H-isochromen-1-one analogues displayed antioxidant activities in 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay. Almost, all the 3-phenyl-1H-isochromen-1-one analogues exhibited potent AA-induced antiplatelet activity; few of them displayed 7-folds more activity as compared to aspirin. Further, in silico analysis validated the wet results. Conclusion: We disclose the first detailed study for the identification of 3-phenyl-1H-isochromen-1-one analogues as highly potent antioxidant as well as antiplatelet agents. The article describes the scaffold designing, synthesis, bioevaluation, structure-activity relationship and in silico studies of pharmaceutically privileged bioactive 3-phenyl-1H-isochromen-1-one class of heterocycles.


2018 ◽  
Vol 151 ◽  
pp. 585-600 ◽  
Author(s):  
Mohamed G. Temraz ◽  
Perihan A. Elzahhar ◽  
Alaa El-Din A. Bekhit ◽  
Adnan A. Bekhit ◽  
Hala F. Labib ◽  
...  

2021 ◽  
pp. 105123
Author(s):  
Derya Osmaniye ◽  
Şennur Görgülü ◽  
Begum Nurpelin Saglik ◽  
Serkan Levent ◽  
Yusuf Ozkay ◽  
...  

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