Chong Y - Search Results

1

Synthesis and anti-hepatitis C virus (HCV) activity of 3'-C-substituted-methyl pyrimidine and purine nucleosides.

Choi WJ, Kim YM, Kim HO, Lee HW, Kim DE, Park KS, Chong Y, Jeong LS. Choi WJ, et al. Among authors: chong y. Bioorg Med Chem. 2010 Jul 1;18(13):4812-20. doi: 10.1016/j.bmc.2010.05.002. Epub 2010 May 31. Bioorg Med Chem. 2010. PMID: 20627592

2

L-nucleosides: antiviral activity and molecular mechanism.

Gumina G, Chong Y, Choo H, Song GY, Chu CK. Gumina G, et al. Among authors: chong y. Curr Top Med Chem. 2002 Oct;2(10):1065-86. doi: 10.2174/1568026023393138. Curr Top Med Chem. 2002. PMID: 12171513 Review.

3

Stereoselective synthesis and antiviral activity of D-2',3'-didehydro-2',3'-dideoxy-2'-fluoro-4'-thionucleosides.

Chong Y, Choo H, Choi Y, Mathew J, Schinazi RF, Chu CK. Chong Y, et al. J Med Chem. 2002 Oct 24;45(22):4888-98. doi: 10.1021/jm020246+. J Med Chem. 2002. PMID: 12383014

4

Synthesis, anti-HIV activity, and molecular mechanism of drug resistance of L-2',3'-didehydro-2',3'-dideoxy-2'-fluoro-4'-thionucleosides.

Choo H, Chong Y, Choi Y, Mathew J, Schinazi RF, Chu CK. Choo H, et al. Among authors: chong y. J Med Chem. 2003 Jan 30;46(3):389-98. doi: 10.1021/jm020376i. J Med Chem. 2003. PMID: 12540238

5

Synthesis, structure-activity relationships, and drug resistance of beta-d-3'-fluoro-2',3'-unsaturated nucleosides as anti-HIV Agents.

Zhou W, Gumina G, Chong Y, Wang J, Schinazi RF, Chu CK. Zhou W, et al. Among authors: chong y. J Med Chem. 2004 Jun 17;47(13):3399-408. doi: 10.1021/jm040027j. J Med Chem. 2004. PMID: 15189036

6

Synthesis of the 5-phosphono-pent-2-en-1-yl nucleosides: a new class of antiviral acyclic nucleoside phosphonates.

Choo H, Beadle JR, Chong Y, Trahan J, Hostetler KY. Choo H, et al. Among authors: chong y. Bioorg Med Chem. 2007 Feb 15;15(4):1771-9. doi: 10.1016/j.bmc.2006.11.038. Epub 2006 Nov 30. Bioorg Med Chem. 2007. PMID: 17166725 Free PMC article.

7

Effects of the aryl linker and the aromatic substituent on the anti-HCV activities of aryl diketoacid (ADK) analogues.

Kim J, Kim KS, Lee HS, Park KS, Park SY, Kang SY, Lee SJ, Park HS, Kim DE, Chong Y. Kim J, et al. Among authors: chong y. Bioorg Med Chem Lett. 2008 Aug 15;18(16):4661-5. doi: 10.1016/j.bmcl.2008.07.008. Epub 2008 Jul 9. Bioorg Med Chem Lett. 2008. PMID: 18644717

8

Identification of novel HCV RNA-dependent RNA polymerase inhibitors using pharmacophore-guided virtual screening.

Kim J, Kim KS, Kim DE, Chong Y. Kim J, et al. Among authors: chong y. Chem Biol Drug Des. 2008 Dec;72(6):585-91. doi: 10.1111/j.1747-0285.2008.00730.x. Chem Biol Drug Des. 2008. PMID: 19090925

9

In vitro solubility, stability and permeability of novel quercetin-amino acid conjugates.

Kim MK, Park KS, Yeo WS, Choo H, Chong Y. Kim MK, et al. Among authors: chong y. Bioorg Med Chem. 2009 Feb 1;17(3):1164-71. doi: 10.1016/j.bmc.2008.12.043. Epub 2008 Dec 25. Bioorg Med Chem. 2009. PMID: 19128975

10

Aryl diketoacids (ADK) selectively inhibit duplex DNA-unwinding activity of SARS coronavirus NTPase/helicase.

Lee C, Lee JM, Lee NR, Jin BS, Jang KJ, Kim DE, Jeong YJ, Chong Y. Lee C, et al. Among authors: chong y. Bioorg Med Chem Lett. 2009 Mar 15;19(6):1636-8. doi: 10.1016/j.bmcl.2009.02.010. Epub 2009 Feb 9. Bioorg Med Chem Lett. 2009. PMID: 19233643 Free PMC article.

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