Collect. Czech. Chem. Commun.
2009, 74, 1361-1373
https://doi.org/10.1135/cccc2009054
Published online 2009-09-16 22:07:00
QSAR analysis of 2-oxo-1,2,3,4-tetrahydropyrimidine analogues of antibacterials
Ramesh L. Sawanta,* and Manish S. Bhatiab
a Department of Pharmaceutical Chemistry, Pd. Dr. Vithalrao Vikhe Patil Foundation’s College of Pharmacy, Vilad Ghat, Post-MIDC, Ahmednagar-414111, Maharashtra, India
b Department of Pharmaceutical Chemistry, Bharati Vidyapeeth College of Pharmacy, Near Chitranagari, Kolhapur-416013, Maharashtra, India
References
1. Indian Drugs 2004, 41, 524.
G. K., Sen S., Rajendra B.:
2. Science 1992, 257, 1050.
< M. L.: https://doi.org/10.1126/science.257.5073.1050>
3. Curr. Top. Med. Chem. 2008, 8, 1676.
< D. H., Prado P. F., Ubeira F. M.: https://doi.org/10.2174/156802608786786543>
4. Curr. Top. Med. Chem. 2007, 7, 1015.
< D. H., Vilar S., Santana L., Uriarte E.: https://doi.org/10.2174/156802607780906771>
5. Molecules 1998, 3, 1.
< C. O.: https://doi.org/10.3390/30100001>
6. Bioorg. Med. Chem. Lett. 2000, 10, 1917.
< J. C., Glass K. L., Selnick H. G., Freidinger R. M., Chang R. S. L., O’Malley S. S., Woyden C.: https://doi.org/10.1016/S0960-894X(00)00374-7>
7. J. Org. Chem. 1995, 60, 1182.
< A. D., Kumar N. V., Kokke W. C., Bean M. F., Freyer A. J., Debrose C., Mai S., Trunch A., Falkner D. J., Carte B., Breen A. L., Hertzberg R. P., Johnston R. K., Westely J. W., Ports B. C. M.: https://doi.org/10.1021/jo00110a021>
8. J. Med. Pharm. Chem. 1961, 3, 215.
< E. W., Hull R.: https://doi.org/10.1021/jm50015a002>
9. Tetrahedron 2000, 56, 1859.
< C. O., Shishkin O. V., Uray G., Verdino P.: https://doi.org/10.1016/S0040-4020(00)00116-2>
10. Acc. Chem. Res. 2000, 33, 879.
< C. O.: https://doi.org/10.1021/ar000048h>
11. Arch. Pharm. 1995, 328, 169.
< B., Akgun H., Ertan M., Sara Y., Ertekin N.: https://doi.org/10.1002/ardp.19953280215>
12. J. Med. Chem. 1998, 41, 5320.
< D., Wetzel J. M., Miao S. W., Marzabad M. R., Chiu G., Wang W. C., Hong X., Fang J., Forry C., Branchek T. A., Heydora W. E., Chang R. S. L., Broten T., Schora T., Gluchowski C.: https://doi.org/10.1021/jm980506g>
13. Arch. Pharm. 2000, 333, 415.
< B., Yarim M., Sarac S., Ertan M., Kelicen P., Altinok G., Demirdamar R.: https://doi.org/10.1002/1521-4184(200012)333:12<415::AID-ARDP415>3.0.CO;2-E>
14. Arch. Pharm. 2001, 334, 79.
< M. H., Park J. G., Lee M. J.: https://doi.org/10.1002/1521-4184(200103)334:3<79::AID-ARDP79>3.0.CO;2-7>
15. Eur. J. Med. Chem. 2000, 35, 1043.
< C. O.: https://doi.org/10.1016/S0223-5234(00)01189-2>
16. Curr. Top. Med. Chem. 2008, 8, 1555.
< S., Cozz G., Moro S.: https://doi.org/10.2174/156802608786786624>
17. Bull. Chem. Soc. Ethiopia 2008, 22, 391.
< R. L., Bhatia M. S.: https://doi.org/10.4314/bcse.v22i3.61218>
18. Int. J. Chem. Sci. 2008, 6, 45.
R. L., Bhatia M. S.:
19. Antimicrob. Agents Chemother. 1978, 10, 335.
L. A., Thornsberry C.:
20. Arkivoc 2006, 13, 73.
< B., Kumari M., Dhake A., Sundaravelan C.: https://doi.org/10.3998/ark.5550190.0007.d08>
21. J. Braz. Chem. Soc. 2004, 15, 165.
< D., Lopes F. A., Da Silva V. S. S., Canto K. F. S., Montes M. G., D’Oca, Godoi M. N.: https://doi.org/10.1590/S0103-50532004000200002>
22. Indian J. Chem., B 2004, 43, 1485.
S., Saini A., Sandhu J. S.: