Browse > Article
http://dx.doi.org/10.5012/bkcs.2004.25.7.1003

Alkoxybenzylcyanoguanidine Analogs as a Novel Class of Inhibitors for Restenosis  

Lee, Sun-Kyung (Medicinal Science Division, Korea Research Institute of Chemical Technology)
Yi, Kyu-Yang (Medicinal Science Division, Korea Research Institute of Chemical Technology)
Hwang, Sun-Kyung (Medicinal Science Division, Korea Research Institute of Chemical Technology)
Suh, Jee-Hee (Medicinal Science Division, Korea Research Institute of Chemical Technology)
Lee, Byung-Ho (Medicinal Science Division, Korea Research Institute of Chemical Technology)
Yoo, Sung-Eun (Medicinal Science Division, Korea Research Institute of Chemical Technology)
Publication Information
Abstract
A novel class of alkoxybenzylcyanoguanidine analogs as the inhibitors of restenosis was discovered, which showed the inhibitory effects on angiotensin II-induced cell proliferation, determined by $[^3H]$thymidine incorporation method. The compound, N'-(4-nitrophenyl)guanidine analog 19, showed 62% inhibition of $[^3H]$thymidine incorporation at 1 ${\mu}M$ concentration. In addition, the compound 19 inhibited intimal thickening dose-dependently after balloon injury, which suggests the therapeutic potential for restenosis.
Keywords
Alkoxybenzylcyanoguanidine; PTCA; Restenosis; Cell proliferation; Intimal hyperplasia;
Citations & Related Records

Times Cited By Web Of Science : 0  (Related Records In Web of Science)
Times Cited By SCOPUS : 0
연도 인용수 순위
  • Reference
1 Orford, J. L.; Selwyn, A. P.; Ganz, P.; Poma, J. J.; Rogers, C. Am. J. Cardiol. 2000, 86(suppl), 6H.   DOI   ScienceOn
2 Omura, K.; Swern, D. Tetrahedron 1978, 34, 1651.   DOI   ScienceOn
3 Bunkenburg, B.; van Amelsvoort, T.; Rogg, H.; Wood, J. M. Hypertension 1992, 20, 746.   DOI
4 Kornowsk, R.; Hong, M. K.; Tio, F. O.; Bramwell, O.; Wu, H.; Leon, M. B. J. Am. Coll. Cardiol. 1998, 31, 224.   DOI   ScienceOn
5 Durand, E.; Mallat, Z.; Addad, F.; Vilde, F.; Desnos, M.; Guerot, C.; Tedgui, A.; Lafont, A. J. Am. Coll. Cardiol. 2002, 39, 1680.   DOI   ScienceOn
6 Scott, N. Circulation 1995, 93, 2178.
7 Pan, S.-L.; Huang, Y.-W.; Guh, J.-H.; Chang, Y.-L.; Peng, C.-Y.; Teng, C. M. Biochem. Pharmacol. 2003, 65, 1897.   DOI   ScienceOn
8 Clowes, A. W.; Schwartz, S. M. Circ. Res. 1985, 56, 139.   DOI   ScienceOn
9 Atwal, K. S.; Ahmed, S. Z.; O'Reilly, B. C. Tetrahedron Lett. 1989, 30, 7313.   DOI   ScienceOn
10 Neumann, F. J.; Ott, I.; Gawaz, M.; Puchner, G.; Schomig, A. J. Am. Coll. Cardiol. 1996, 27, 819.   DOI   ScienceOn
11 Virone-Oddos, A.; Desangle, V.; Provost, D.; Cazes, M.; Caussade, F.; Cloarec, A. Br. J. Pharmacol. 1997, 120, 488.   DOI   ScienceOn
12 Bult, H. TiPS 2000, 21, 274.
13 Pretre, R.; Orford, J. L. JAMA 2001, 285, 992.   DOI   ScienceOn
14 Faxon, D. P.; Williams, D. O.; Yeh, W.; Mehra, A.; Holubokov, R.; Detre, K. J. Am. Coll. Cardiol. 1999, 33(suppl A), 91A.
15 Rogers, C.; Edelman, E. R.; Simon, D. I. Proc. Natl. Acad. Sci. USA 1998, 95, 10134.   DOI
16 Simon, D. I.; Chen, Z.; Seifert, P.; Edelmann, E.; Ballantyne, C. M.; Rogers, C. Circulation 1998, 98, 238.
17 Yoo, S.-e.; Yi, K. Y.; Lee, S.; Suh, J.; Kim, N.; Lee, B. H.; Seo, H. W.; Kim, S.-O.; Lee, D.-H.; Lim, H.; Shin, H. S. J. Med. Chem. 2001, 44, 4207.   DOI   ScienceOn
18 Brooks, G.; La Thangue, N. B. DDT 1999, 4, 455.   DOI   ScienceOn
19 Nair, S. V.; McEwan, J. R. Int. J. Biochem. & Cell. Biol. 2003, 35, 1399.   DOI   ScienceOn
20 Lincoff, A. M.; Topol, E. J.; Ellis, S. G. Circulation 1994, 90, 2070.   DOI   ScienceOn