Author(s): Mahesh Bhat, Madhu N, Sagar B K, E. Vijay Sekhar

Email(s): maheshbhat08@gmail.com

DOI: 10.5958/0974-360X.2019.00288.9   

Address: Mahesh Bhat1*, Madhu N2, Sagar B K3, E. Vijay Sekhar2
1Post Graduate, Department of Chemistry, Bangurnagar Arts, Science and Commerce College, Dandeli- 581325, Karnataka, India
2PG Department of Chemistry, JSS College for Women, Saraswathipuram, Mysore-570 009 Karnataka, India
3DOS in Chemistry, University of Mysore, Manasagangothri, Mysore-570 006, Karnataka, India
*Corresponding Author

Published In:   Volume - 12,      Issue - 4,     Year - 2019


ABSTRACT:
Guanidine’s are major functionality in natural and synthetic compound, which exhibit a variety of activities like antidiabetic, antimicrobial, antiviral, anticancer, antibiotic and anti-inflammatory etc. The wide spread of guanidine compounds in the field of pharmaceutical, makes them as one of the attractive pharmacophores. The presence of the -CN3 group in guanidine compounds makes them to have efficient affinity towards various substituents with wide range of biochemical activities. In the present study, novel Sulfisoxazole guanidinyl derivatives were synthesized and characterized by LCMS and NMR spectral studies. The synthesized compounds were screened for anti-TB and anti-oxidant activities. It was found that compounds with electron donating groups exhibited superior activity.


Cite this article:
Mahesh Bhat, Madhu N, Sagar B K, E. Vijay Sekhar. Sulfisoxazole Guanidinyl Derivatives: Synthesis, Characterization and Docking Studies for potential Anti-TB agents. Research J. Pharm. and Tech. 2019; 12(4):1726-1730. doi: 10.5958/0974-360X.2019.00288.9

Cite(Electronic):
Mahesh Bhat, Madhu N, Sagar B K, E. Vijay Sekhar. Sulfisoxazole Guanidinyl Derivatives: Synthesis, Characterization and Docking Studies for potential Anti-TB agents. Research J. Pharm. and Tech. 2019; 12(4):1726-1730. doi: 10.5958/0974-360X.2019.00288.9   Available on: https://www.rjptonline.org/AbstractView.aspx?PID=2019-12-4-43


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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

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