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Journal Abstract Search

130 related items for PubMed ID: 16876404

  • 1. Morpholin-2-one derivatives as novel selective T-type Ca2+ channel blockers.
    Ku IW, Cho S, Doddareddy MR, Jang MS, Keum G, Lee JH, Chung BY, Kim Y, Rhim H, Kang SB.
    Bioorg Med Chem Lett; 2006 Oct 01; 16(19):5244-8. PubMed ID: 16876404
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  • 2. Synthesis and biological activity of 3,4-dihydroquinazolines for selective T-type Ca2+ channel blockers.
    Rhim H, Lee YS, Park SJ, Chung BY, Lee JY.
    Bioorg Med Chem Lett; 2005 Jan 17; 15(2):283-6. PubMed ID: 15603940
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  • 3. Synthesis and SAR studies of a novel series of T-type calcium channel blockers.
    Park SJ, Park SJ, Lee MJ, Rhim H, Kim Y, Lee JH, Chung BY, Lee JY.
    Bioorg Med Chem; 2006 May 15; 14(10):3502-11. PubMed ID: 16434203
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  • 5. 3D pharmacophore based virtual screening of T-type calcium channel blockers.
    Doddareddy MR, Choo H, Cho YS, Rhim H, Koh HY, Lee JH, Jeong SW, Pae AN.
    Bioorg Med Chem; 2007 Jan 15; 15(2):1091-105. PubMed ID: 17074493
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  • 8. Synthesis and biological evaluation of novel T-type Ca2+ channel blockers.
    Jung HK, Doddareddy MR, Cha JH, Rhim H, Cho YS, Koh HY, Jung BY, Pae AN.
    Bioorg Med Chem; 2004 Aug 01; 12(15):3965-70. PubMed ID: 15246072
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  • 9. Lead discovery and optimization of T-type calcium channel blockers.
    Park JH, Choi JK, Lee E, Lee JK, Rhim H, Seo SH, Kim Y, Doddareddy MR, Pae AN, Kang J, Roh EJ.
    Bioorg Med Chem; 2007 Feb 01; 15(3):1409-19. PubMed ID: 17150365
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  • 12. Synthesis and evaluation of alpha,alpha'-disubstituted phenylacetate derivatives for T-type calcium channel blockers.
    Lee HK, Lee YS, Roh EJ, Rhim H, Lee JY, Shin KJ.
    Bioorg Med Chem Lett; 2008 Aug 01; 18(15):4424-7. PubMed ID: 18625556
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  • 13. Five different profiles of dihydropyridines in blocking T-type Ca(2+) channel subtypes (Ca(v)3.1 (alpha(1G)), Ca(v)3.2 (alpha(1H)), and Ca(v)3.3 (alpha(1I))) expressed in Xenopus oocytes.
    Furukawa T, Nukada T, Namiki Y, Miyashita Y, Hatsuno K, Ueno Y, Yamakawa T, Isshiki T.
    Eur J Pharmacol; 2009 Jun 24; 613(1-3):100-7. PubMed ID: 19401195
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  • 14. Scaffold-based design and synthesis of potent N-type calcium channel blockers.
    Zamponi GW, Feng ZP, Zhang L, Pajouhesh H, Ding Y, Belardetti F, Pajouhesh H, Dolphin D, Mitscher LA, Snutch TP.
    Bioorg Med Chem Lett; 2009 Nov 15; 19(22):6467-72. PubMed ID: 19815411
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  • 16. Discovery of potent T-type calcium channel blocker.
    Seo HN, Choi JY, Choe YJ, Kim Y, Rhim H, Lee SH, Kim J, Joo DJ, Lee JY.
    Bioorg Med Chem Lett; 2007 Nov 01; 17(21):5740-3. PubMed ID: 17869104
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  • 17. Synthesis and biological evaluation of oxazole derivatives as T-type calcium channel blockers.
    Lee JE, Koh HY, Seo SH, Baek YY, Rhim H, Cho YS, Choo H, Pae AN.
    Bioorg Med Chem Lett; 2010 Jul 15; 20(14):4219-22. PubMed ID: 20621730
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  • 18. Synthesis and SAR study of T-type calcium channel blockers. Part II.
    Choe YJ, Seo HN, Jung SY, Rhim H, Kim J, Choo DJ, Lee JY.
    Arch Pharm (Weinheim); 2008 Oct 15; 341(10):661-4. PubMed ID: 18816587
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  • 19. C101, a novel 4-amino-piperidine derivative selectively blocks N-type calcium channels.
    Zhang S, Su R, Zhang C, Liu X, Li J, Zheng J.
    Eur J Pharmacol; 2008 Jun 10; 587(1-3):42-7. PubMed ID: 18468596
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  • 20. Ca2+ channel subtypes and pharmacology in the kidney.
    Hayashi K, Wakino S, Sugano N, Ozawa Y, Homma K, Saruta T.
    Circ Res; 2007 Feb 16; 100(3):342-53. PubMed ID: 17307972
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