Collect. Czech. Chem. Commun.
2011, 76, 803-813
https://doi.org/10.1135/cccc2011019
Published online 2011-06-15 11:29:17
QSAR study of a series of cholesteryl ester transfer protein inhibitors
Mahesh T. Chhabriaa, Bhanubhai N. Suhagiaa, Appaji B. Mandhareb and Pathik S. Brahmkshatriyaa,*
a Department of Pharmaceutical Chemistry, L M College of Pharmacy, Navrangpura, Ahmedabad-380 009, Gujarat, India
b Torrent Research Centre, Torrent Pharmaceuticals Ltd., Medicinal Chemistry-Drug Discovery, Gandhinagar-382 428, Gujarat, India
References
1. M. T., Brahmkshatriya P. S.: Curr. Opin. Invest. Drugs 2006, 7, 820.
2. P. S., Chhabria M. T., Jani M. H.: J. Enzyme Inhib. Med. Chem. 2006, 21, 1.
<https://doi.org/10.1080/14756360500337634>
3. M. A., Wilson J. P.: Ann. Pharmacother. 2002, 36, 288.
<https://doi.org/10.1345/aph.1A289>
4. A. R.: J. Lipid Res. 1993, 34, 1255.
5. P. J., Brewer H. B., Chapman M. J., Hennekens C. H., Rader D. J., Tall A. R.: Arterioscler. Thromb. Vasc. Biol. 2003, 23, 160.
<https://doi.org/10.1161/01.ATV.0000054658.91146.64>
6. G. J., Smilde T. J., Van Wissen V., Klerkx A. H. E. M., Zwinderman A. H., Fruchart J. C., Kastelein J. J. P., Stalenhoef A. F. H., Kuivenhoven J. A.: Atherosclerosis 2004, 173, 261.
<https://doi.org/10.1016/j.atherosclerosis.2003.11.020>
7. R., Mann C. J., Tall A. R., Hogue M., Martin L., Milne R. W., Marcel Y. L.: Arterioscler. Thromb. Vasc. Biol. 1991, 11, 797.
<https://doi.org/10.1161/01.ATV.11.4.797>
8. P., Appel G. B., Ginsberg H. N., Tall A. R.: J. Lipid Res. 1992, 33, 1817.
9. P. J., Kastelein J. J.: J. Am. Coll. Cardiol. 2006, 47, 492.
<https://doi.org/10.1016/j.jacc.2005.09.042>
10. G. J., Klerkx A. H., Stroes E. S., Stalenhoef A. F. H., Kastelein J. J. P., Kuivenhoven J. A.: J. Lipid Res. 2004, 45, 1967.
<https://doi.org/10.1194/jlr.R400007-JLR200>
11. M. T., Suhagia B. N., Brahmkshatriya P. S.: Recent Patents Cardiovasc. Drug Discov. 2007, 2, 214.
<https://doi.org/10.2174/157489007782418973>
12. E. A., Roth E. M., Rhyne J. M., Burgess T., Kallend D., Robinson J. G.: Eur. Heart J. 2010, 31, 480.
<https://doi.org/10.1093/eurheartj/ehp601>
13. A. R., Yvan-Charvet L., Wang N.: Arterioscler. Thromb. Vasc. Biol. 2007, 27, 257.
<https://doi.org/10.1161/01.ATV.0000256728.60226.77>
14. L., Lin W. O., Jiang J. H., Shen G. L., Yu R. Q.: Eur. J. Pharm. Sci. 2005, 25, 245.
<https://doi.org/10.1016/j.ejps.2005.02.016>
15. H. Z. , Wang T., Zhang K. J., Hua Z. D., Fan B. T.: Bioorg. Med. Chem. 2006, 14, 4834.
<https://doi.org/10.1016/j.bmc.2006.03.019>
16. P. M., Geethababu S. K., Doble M.: Chem. Biol. Drug Res. 2008, 71, 447.
<https://doi.org/10.1111/j.1747-0285.2008.00657.x>
17. J. X., Shen Q., Jiang J. H., Shen G. L., Yu R. Q.: J. Pharm. Biomed. Anal. 2004, 35, 679.
<https://doi.org/10.1016/j.jpba.2004.02.026>
18. A.: J. Chemometrics 1988, 2, 211.
<https://doi.org/10.1002/cem.1180020306>
19. A. K., Prathipati P.: SAR QSAR Environ. Res. 2003, 14, 433.
<https://doi.org/10.1080/10629360310001624015>
20. D., Hopfinger A. J.: J. Chem. Inf. Comput. Sci. 1994, 34, 854.
<https://doi.org/10.1021/ci00020a020>
21. V. M., Karki R. J.: Bioorg. Med. Chem. 2001, 9, 3153.
22. D. H., Lee S. K., Kim B. T., No K. T.: Bull. Korean Chem. Soc. 2001, 22, 388.
23. K., Bhattacharya P.: Bioorg. Med. Chem. Lett. 2005, 15, 3737.
<https://doi.org/10.1016/j.bmcl.2005.04.030>
24. Sikorski J. A.: (Searle and Co.) WO1999/14204.
25. Discovery Studio 2.1. Accelrys Inc., 6985 Scranton Road, San Diego, CA, USA.
26. M., Khadikar P. V., Scozzafava A., Supuran A.: Bioorg. Med. Chem. Lett. 2004, 14, 3283.
<https://doi.org/10.1016/j.bmcl.2004.03.099>
27. P. P., Roy K.: QSAR Comb. Sci. 2007, 27, 302.
<https://doi.org/10.1002/qsar.200710043>
28. H., Maeda K., Yamasaki T., Okamoto H., Uchida I.: J. Med. Chem. 2000, 43, 3566.
<https://doi.org/10.1021/jm000224s>
29. D. T., Jurs P. C.: Anal. Chem. 1990, 62, 2323.
<https://doi.org/10.1021/ac00220a013>

