Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2007 Oct 30;12(10):2413-26.
doi: 10.3390/12102413.

Antibacterial activity of some 3-(arylideneamino)-2-phenylquinazoline-4(3H)-ones: synthesis and preliminary QSAR studies

Affiliations

Antibacterial activity of some 3-(arylideneamino)-2-phenylquinazoline-4(3H)-ones: synthesis and preliminary QSAR studies

Ashis Kumar Nanda et al. Molecules. .

Abstract

Synthesis of ten 3-(arylideneamino)-2-phenylquinazoline-4(3H)-ones is reported. All the compounds contained a common phenyl group at the 2-position, while the substituents on the arylideneamino group were varied. The compounds were investigated for their antimicrobial activity against both Gram-positive (Staphylococcus aureus 6571 and Bacillus subtilis) and Gram-negative bacteria (Escherichia coli K12 and Shigella dysenteriae 6) using a turbidometric assay method. It was found that the incorporation of the 3-arylideneamino substituent enhanced the anti-bacterial activity of the quinazolone system. The preliminary QSAR studies were done using some computer derived property descriptors, calculated values of partition coefficients as well as usual Hammett's sigma constants and the substituent's molar refractivity.

PubMed Disclaimer

Figures

Scheme 1
Scheme 1
Figure 1
Figure 1
Juxtaposed pictures of the 2D-NMR spectra of compound 3j.

Similar articles

Cited by

References

    1. Spirkova K., Stankovsky S., Mrvova A., Cipak L. Synthesis and Biological Activity of Some 2-substituted Quinazolin-4-ones. Chem. Pap. 1999;53:272–275.
    1. Alagarsamy V., Giridhar R., Yadav H. R., Revathi R., Rukmani K., De Clercq E. Anti HIV, antibacterial and antifungal activities of some novel1,4-disubstituted-1,2,4-triazolo[4,3a] quinazolin-5(4h)-ones. Indian J. Pharm. Sci. 2006;68:532–535. doi: 10.4103/0250-474X.27840. - DOI
    1. Srivastava V. K., Singh A., Gucati A., Shankar K. Antiparkinsonian agent from qunazonyl thioazolidinones and azetidinones. Indian J. Chem. 1987;26:652–656.
    1. Gupta D. P., Ahmed S., Kumar A., Shankar K. Newer Quinazolinone Derivatives as Anthelmintic Agents. Indian J. Chem. 1988;27:1060–1062.
    1. Jatav V., Mishra P., Kaswa S., Stabes J. P. Synthesis and CNS depressant activity of some novel 3-[5-substituted 1,3,4-thiadiazole-2-yl]-2-styryl quinazoline-4(3H)-ones. Eur. J. Med. Chem. 2007 ? - PubMed

MeSH terms