Abstract
A series of pyrimido[4,5-b]quinolin-2,4(1H,3H)-dione derivatives (5-deazaalloxazines) was synthesized by the reaction of various substituted 2-chloroquinolin-3-carboxylic acids with urea/thiourea. The structure of these newly synthesized compounds was characterized by standard spectroscopic and analytical techniques. The antimicrobial activities of the title compounds were evaluated against Gram-positive and Gram-negative bacteria and fungi using a micro dilution procedure and compared with those of standard drugs. The minimum inhibitory concentration of the derivative compounds was also determined by measuring their in vitro activities against both bacteria and fungi strains.
Graphical Abstract
Newly synthesized pyrimido[4,5-b]quinolin-2,4(1H,3H)-dione derivatives structure was elucidated on the basis of standard spectroscopic and analytical techniques. In vitro activities of title compounds were evaluated against Gram-positive, Gram-negative bacteria and fungi using micro dilution procedure.
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Acknowledgments
The financial support by the Government of Tamilnadu, India, (to author V. N.) is gratefully acknowledged. The authors thank Changwon National University, Changwon, Republic of Korea, and the Indian Institute of Technology, Chennai, India, for the spectral analyses.
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Nadaraj, V., Selvi, S.T., Mohan, S. et al. Microwave-assisted synthesis and pharmacological studies of novel 5-deazaalloxazine derivatives. Med Chem Res 21, 2911–2919 (2012). https://doi.org/10.1007/s00044-011-9811-1
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DOI: https://doi.org/10.1007/s00044-011-9811-1