Oh KS - Search Results

1

Accurate prediction of protein-ligand interactions by combining physical energy functions and graph-neural networks.

Hong Y, Ha J, Sim J, Lim CJ, Oh KS, Chandrasekaran R, Kim B, Choi J, Ko J, Shin WH, Lee J. Hong Y, et al. Among authors: oh ks. J Cheminform. 2024 Nov 4;16(1):121. doi: 10.1186/s13321-024-00912-2. J Cheminform. 2024. PMID: 39497201 Free PMC article.

2

Synthesis and SAR investigations of novel 2-arylbenzimidazole derivatives as melanin-concentrating hormone receptor 1 (MCH-R1) antagonists.

Lim CJ, Kim N, Lee EK, Lee BH, Oh KS, Yoo SE, Yi KY. Lim CJ, et al. Among authors: oh ks. Bioorg Med Chem Lett. 2011 Apr 15;21(8):2309-12. doi: 10.1016/j.bmcl.2011.02.099. Epub 2011 Feb 26. Bioorg Med Chem Lett. 2011. PMID: 21420863

3

4-arylphthalazin-1(2H)-one derivatives as potent antagonists of the melanin concentrating hormone receptor 1 (MCH-R1).

Lim CJ, Kim SH, Lee BH, Oh KS, Yi KY. Lim CJ, et al. Among authors: oh ks. Bioorg Med Chem Lett. 2012 Jan 1;22(1):427-30. doi: 10.1016/j.bmcl.2011.10.111. Epub 2011 Nov 10. Bioorg Med Chem Lett. 2012. PMID: 22137790

4

Discovery of novel scaffolds for Rho kinase 2 inhibitor through TRFRET-based high throughput screening assay.

Oh KS, Mun J, Cho JE, Lee S, Yi KY, Lim CJ, Lee JS, Park WJ, Lee BH. Oh KS, et al. Comb Chem High Throughput Screen. 2013 Jan;16(1):37-46. doi: 10.2174/1386207311316010006. Comb Chem High Throughput Screen. 2013. PMID: 22934984

5

Synthesis and SAR study of pyrrolo[3,4-b]pyridin-7(6H)-one derivatives as melanin concentrating hormone receptor 1 (MCH-R1) antagonists.

Lim CJ, Kim JY, Lee BH, Oh KS, Yi KY. Lim CJ, et al. Among authors: oh ks. Bioorg Med Chem Lett. 2013 Mar 15;23(6):1736-9. doi: 10.1016/j.bmcl.2013.01.053. Epub 2013 Jan 24. Bioorg Med Chem Lett. 2013. PMID: 23411080

6

Synthesis and structure-activity relationship of naphtho[1,2-b]furan-2-carboxamide derivatives as melanin concentrating hormone receptor 1 antagonists.

Lim CJ, Choi JY, Lee BH, Oh KS, Yi KY. Lim CJ, et al. Among authors: oh ks. Chem Pharm Bull (Tokyo). 2013;61(12):1239-47. doi: 10.1248/cpb.c13-00486. Chem Pharm Bull (Tokyo). 2013. PMID: 24292786 Free article.

7

4-Substituted quinazoline derivatives as novel EphA2 receptor tyrosine kinase inhibitors.

Lim CJ, Oh KS, Ha JD, Lee JH, Seo HW, Chae CH, Kim DG, Lee MJ, Lee BH. Lim CJ, et al. Among authors: oh ks. Bioorg Med Chem Lett. 2014 Sep 1;24(17):4080-3. doi: 10.1016/j.bmcl.2014.07.081. Epub 2014 Aug 6. Bioorg Med Chem Lett. 2014. PMID: 25124116

8

Synthesis and SAR of thieno[3,2-b]pyridinyl urea derivatives as urotensin-II receptor antagonists.

Lim CJ, Oh SA, Lee BH, Oh KS, Yi KY. Lim CJ, et al. Among authors: oh ks, oh sa. Bioorg Med Chem Lett. 2014 Dec 15;24(24):5832-5835. doi: 10.1016/j.bmcl.2014.09.089. Epub 2014 Oct 28. Bioorg Med Chem Lett. 2014. PMID: 25452001

9

Benzo[b]thiophene-2-carboxamide derivatives as potent urotensin-II receptor antagonists.

Lim CJ, Woo SE, Ko SI, Lee BH, Oh KS, Yi KY. Lim CJ, et al. Among authors: oh ks. Bioorg Med Chem Lett. 2016 Oct 1;26(19):4684-4686. doi: 10.1016/j.bmcl.2016.08.049. Epub 2016 Aug 26. Bioorg Med Chem Lett. 2016. PMID: 27597245

10

A urotensin II receptor antagonist, KR36676, decreases vascular remodeling and inflammation in experimental pulmonary hypertension.

Lee JH, Park BK, Oh KS, Yi KY, Lim CJ, Seo HW, Lee BH. Lee JH, et al. Among authors: oh ks. Int Immunopharmacol. 2016 Nov;40:196-202. doi: 10.1016/j.intimp.2016.09.002. Epub 2016 Sep 6. Int Immunopharmacol. 2016. PMID: 27611861

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