Design, synthesis, characterization, antibacterial and antifungal activities of a novel class of 5,7-diaryl-4,4-dimethyl-4,5,6,7- tetrahydropyridino[3,4-d]-1,2,3-selenadiazoles

25Citations
Citations of this article
9Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Compound 26 is more potent against Escherichia coli. and 24 is more active against Staphylococcus aureus, β-Heamolytic streptococcus, Vibreo cholerae, Salmonella typhii, and Shigella flexneri than the standard drug ciprofloxacin. Moreover, of all the compounds tested, 26 is more effective against Aspergillus flavus and Mucor, than the standard drug fluconazole.

Cite

CITATION STYLE

APA

Gopalakrishnan, M., Sureshkumar, P., Thanusu, J., & Kanagarajan, V. (2008). Design, synthesis, characterization, antibacterial and antifungal activities of a novel class of 5,7-diaryl-4,4-dimethyl-4,5,6,7- tetrahydropyridino[3,4-d]-1,2,3-selenadiazoles. Journal of Enzyme Inhibition and Medicinal Chemistry, 23(3), 347–351. https://doi.org/10.1080/14756360701611498

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free