Kim HO - Search Results

1

Fluorocyclopentenyl-cytosine with broad spectrum and potent antitumor activity.

Choi WJ, Chung HJ, Chandra G, Alexander V, Zhao LX, Lee HW, Nayak A, Majik MS, Kim HO, Kim JH, Lee YB, Ahn CH, Lee SK, Jeong LS. Choi WJ, et al. Among authors: kim ho, kim jh. J Med Chem. 2012 May 10;55(9):4521-5. doi: 10.1021/jm3004009. Epub 2012 May 1. J Med Chem. 2012. PMID: 22524616

2

Synthesis of novel (2R,4R)- and (2S,4S)-iso dideoxynucleosides with exocyclic methylene as potential antiviral agents.

Yoo SJ, Kim HO, Lim Y, Kim J, Jeong LS. Yoo SJ, et al. Among authors: kim ho, kim j. Bioorg Med Chem. 2002 Jan;10(1):215-26. doi: 10.1016/s0968-0896(01)00266-8. Bioorg Med Chem. 2002. PMID: 11738624

3

Synthesis and biological evaluation of novel thioapio dideoxynucleosides.

Moon HR, Kim HO, Lee SK, Choi WJ, Chun MW, Jeong LS. Moon HR, et al. Among authors: kim ho. Bioorg Med Chem. 2002 May;10(5):1499-507. doi: 10.1016/s0968-0896(01)00417-5. Bioorg Med Chem. 2002. PMID: 11886812

4

Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase.

Jeong LS, Yoo SJ, Lee KM, Koo MJ, Choi WJ, Kim HO, Moon HR, Lee MY, Park JG, Lee SK, Chun MW. Jeong LS, et al. Among authors: kim ho. J Med Chem. 2003 Jan 16;46(2):201-3. doi: 10.1021/jm025557z. J Med Chem. 2003. PMID: 12519056

5

Synthesis of fluorinated cyclopentenyladenine as potent inhibitor of S-adenosylhomocysteine hydrolase.

Kim HO, Yoo SJ, Ahn HS, Choi WJ, Moon HR, Lee KM, Chun MW, Jeong LS. Kim HO, et al. Bioorg Med Chem Lett. 2004 May 3;14(9):2091-3. doi: 10.1016/j.bmcl.2004.02.039. Bioorg Med Chem Lett. 2004. PMID: 15080985

6

Synthesis of 5'-substituted fluoro-neplanocin A analogues: importance of a hydrogen bonding donor at 5'-position for the inhibitory activity of S-adenosylhomocysteine hydrolase.

Moon HR, Lee HJ, Kim KR, Lee KM, Lee SK, Kim HO, Chun MW, Jeong LS. Moon HR, et al. Among authors: kim kr, kim ho. Bioorg Med Chem Lett. 2004 Nov 15;14(22):5641-4. doi: 10.1016/j.bmcl.2004.08.047. Bioorg Med Chem Lett. 2004. PMID: 15482939

7

Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-uronamides as highly potent and selective agonists at the human A3 adenosine receptor.

Jeong LS, Lee HW, Jacobson KA, Kim HO, Shin DH, Lee JA, Gao ZG, Lu C, Duong HT, Gunaga P, Lee SK, Jin DZ, Chun MW, Moon HR. Jeong LS, et al. Among authors: kim ho. J Med Chem. 2006 Jan 12;49(1):273-81. doi: 10.1021/jm050595e. J Med Chem. 2006. PMID: 16392812

8

Design, synthesis, and biological activity of N6-substituted-4'-thioadenosines at the human A3 adenosine receptor.

Jeong LS, Lee HW, Kim HO, Jung JY, Gao ZG, Duong HT, Rao S, Jacobson KA, Shin DH, Lee JA, Gunaga P, Lee SK, Jin DZ, Chun MW, Moon HR. Jeong LS, et al. Among authors: kim ho. Bioorg Med Chem. 2006 Jul 15;14(14):4718-30. doi: 10.1016/j.bmc.2006.03.030. Epub 2006 Apr 5. Bioorg Med Chem. 2006. PMID: 16603368

9

Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents.

Yoo BN, Kim HO, Moon HR, Seol SK, Jang SK, Lee KM, Jeong LS. Yoo BN, et al. Among authors: kim ho. Bioorg Med Chem Lett. 2006 Aug 15;16(16):4190-4. doi: 10.1016/j.bmcl.2006.05.089. Epub 2006 Jun 14. Bioorg Med Chem Lett. 2006. PMID: 16781148

10

Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines.

Zhao LX, Yun M, Kim HO, Lee JA, Choi WJ, Lee KM, Lee SK, Lee YB, Ahn CH, Jeong LS. Zhao LX, et al. Among authors: kim ho. Nucleic Acids Symp Ser (Oxf). 2005;(49):107-8. doi: 10.1093/nass/49.1.107. Nucleic Acids Symp Ser (Oxf). 2005. PMID: 17150656

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

3,143 results

Search Page