Comparative Analysis And Identification Of Novel Β-Lactamase Inhibitors

Authors

  • DEEPAK KUMAR JHA School of Biosciences and Technology, VIT University, Vellore, India
  • LIKUN PANDA School of Biosciences and Technology, VIT University, Vellore, India
  • ANAND ANBARASU School of Biosciences and Technology, VIT University, Vellore, India

Keywords:

β-lactamases, NDM1, Sulbactam, Molecular docking, ACE Values

Abstract

β-lactam antibiotics are a broad class of antibiotics, consisting of all antibiotic agents that contain a β-lactam nucleus in its molecular structure. Till now β-lactams like penicillins, cephalosporins, monobactams, and carbapenems have been developed. Resistance to various β-lactam antibiotics among target pathogens were started with its first use.The most widespread and important cause is the destruction of the β-lactam ring, mediated by β-lactamases. Antibiotic resistance can be overcome successfully with the use of β-lactamase inhibitors in combination with β-lactams. Resistance within a few years of the introduction of the antibiotic class seems inevitable that the new antibiotics developed to hit novel targets will also encounter resistance. Hence, it’s needed to identify novel therapeutics to be used as β-lactamase inhibitors. Present study was accomplished to develop novel β-lactamase inhibitors and their comparative study with the already present ones. Most promising results were shown by phenolic derivatives of sulbactam.

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Published

31.12.2011

How to Cite

DEEPAK KUMAR JHA, LIKUN PANDA, & ANAND ANBARASU. (2011). Comparative Analysis And Identification Of Novel Β-Lactamase Inhibitors. International Journal of Pharma and Bio Sciences, 2(4), 77–87. Retrieved from https://ijpbs.net/index.php/journal/article/view/1071

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Research Articles

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