Journal
JOURNAL OF MOLECULAR STRUCTURE
Volume 1175, Issue -, Pages 551-565Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.molstruc.2018.08.018
Keywords
Antimicrobial agents; Docking; Hybrids; Piperazines; Pyrazole; Pyrimidine
Categories
Funding
- UGC, India [F./25-1/2013-14 (BSR)/7-74/2007 (BSR)]
- GUJCOST [F./25-1/2013-14 (BSR)/7-74/2007 (BSR)]
Ask authors/readers for more resources
Utilizing molecular hybridization approach, a progression of novel pyrazolylpyrimidine based N-thio-amide derivatives of piperazine were identified in an effort to develop newer antibacterial and antitubercular agents against the cumulative bacterial resistance. Spectral analysis using Mass, H-1 NMR and C-13 NMR spectral techniques have been studied in order to affirm the structure of synthesized end molecules. Biological evaluation of all synthesized molecules were studied in-vitro for their antibacterial, antituberculosis and antimalarial efficacy against various bacterial and fungal strains, H37Rv and Plasmodium falciparum respectively. Molecular docking and ADME properties prediction study were also carried out for better insights of responsible proteins with the synthesized molecules. Interestingly, some of the pyrazolylpyrimidine based piperazine N-thioamide derivatives exhibited potential antibacterial, antifungal and antimalarial potency. (C) 2018 Elsevier B.V. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available