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2014 1
2015 5
2016 4
2017 1
2020 0
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Did you mean sun ye hong (6 results)?
Role of computer-aided drug design in modern drug discovery.
Macalino SJ, Gosu V, Hong S, Choi S. Macalino SJ, et al. Among authors: hong s. Arch Pharm Res. 2015 Sep;38(9):1686-701. doi: 10.1007/s12272-015-0640-5. Epub 2015 Jul 25. Arch Pharm Res. 2015. PMID: 26208641 Review.
Polymodal Transient Receptor Potential Vanilloid Type 1 Nocisensor: Structure, Modulators, and Therapeutic Applications.
Cui M, Gosu V, Basith S, Hong S, Choi S. Cui M, et al. Among authors: hong s. Adv Protein Chem Struct Biol. 2016;104:81-125. doi: 10.1016/bs.apcsb.2015.11.005. Epub 2016 Jan 4. Adv Protein Chem Struct Biol. 2016. PMID: 27038373 Review.
Transient receptor potential vanilloid type 1 antagonists: a patent review (2011 - 2014).
Lee Y, Hong S, Cui M, Sharma PK, Lee J, Choi S. Lee Y, et al. Among authors: hong s. Expert Opin Ther Pat. 2015 Mar;25(3):291-318. doi: 10.1517/13543776.2015.1008449. Expert Opin Ther Pat. 2015. PMID: 25666693 Review.
α-Substituted 2-(3-fluoro-4-methylsulfonamidophenyl)acetamides as potent TRPV1 antagonists.
Tran PT, Kim HS, Ann J, Kim SE, Kim C, Hong M, Hoang VH, Ngo VT, Hong S, Cui M, Choi S, Blumberg PM, Frank-Foltyn R, Bahrenberg G, Stockhausen H, Christoph T, Lee J. Tran PT, et al. Among authors: hong s. Bioorg Med Chem Lett. 2015 Jun 1;25(11):2326-30. doi: 10.1016/j.bmcl.2015.04.024. Epub 2015 Apr 12. Bioorg Med Chem Lett. 2015. PMID: 25937016 Free PMC article.
2-Sulfonamidopyridine C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists.
Ann J, Ki Y, Yoon S, Kim MS, Lee JU, Kim C, Lee S, Jung A, Baek J, Hong S, Choi S, Pearce LV, Esch TE, Turcios NA, Lewin NE, Ogunjirin AE, Herold BK, McCall AK, Blumberg PM, Lee J. Ann J, et al. Among authors: hong s. Bioorg Med Chem. 2016 Mar 15;24(6):1231-40. doi: 10.1016/j.bmc.2016.01.051. Epub 2016 Jan 28. Bioorg Med Chem. 2016. PMID: 26860926 Free PMC article.
Discovery of N-(3-fluoro-4-methylsulfonamidomethylphenyl)urea as a potent TRPV1 antagonistic template.
Ann J, Sun W, Zhou X, Jung A, Baek J, Lee S, Kim C, Yoon S, Hong S, Choi S, Turcios NA, Herold BK, Esch TE, Lewin NE, Abramovitz A, Pearce LV, Blumberg PM, Lee J. Ann J, et al. Among authors: hong s. Bioorg Med Chem Lett. 2016 Aug 1;26(15):3603-7. doi: 10.1016/j.bmcl.2016.06.010. Epub 2016 Jun 7. Bioorg Med Chem Lett. 2016. PMID: 27317643 Free PMC article.
t-Butyl pyridine and phenyl C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists.
Lee S, Kang DW, Ryu H, Kim C, Ann J, Lee H, Kim E, Hong S, Choi S, Blumberg PM, Frank-Foltyn R, Bahrenberg G, Stockhausen H, Christoph T, Lee J. Lee S, et al. Among authors: hong s. Bioorg Med Chem. 2017 Apr 15;25(8):2451-2462. doi: 10.1016/j.bmc.2017.03.004. Epub 2017 Mar 6. Bioorg Med Chem. 2017. PMID: 28314510 Free PMC article.
5-Lipoxygenase inhibitors suppress RANKL-induced osteoclast formation via NFATc1 expression.
Kang JH, Ting Z, Moon MR, Sim JS, Lee JM, Doh KE, Hong S, Cui M, Choi S, Chang HW, Park Choo HY, Yim M. Kang JH, et al. Among authors: hong s. Bioorg Med Chem. 2015 Nov 1;23(21):7069-78. doi: 10.1016/j.bmc.2015.09.025. Epub 2015 Sep 15. Bioorg Med Chem. 2015. PMID: 26432605
Structure activity relationships of benzyl C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists.
Ann J, Jung A, Kim MY, Kim HM, Ryu H, Kim S, Kang DW, Hong S, Cui M, Choi S, Blumberg PM, Frank-Foltyn R, Bahrenberg G, Stockhausen H, Christoph T, Lee J. Ann J, et al. Among authors: hong s. Bioorg Med Chem. 2015 Nov 1;23(21):6844-54. doi: 10.1016/j.bmc.2015.10.001. Epub 2015 Oct 9. Bioorg Med Chem. 2015. PMID: 26474664 Free PMC article.
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