Jeong LS - Search Results

1

A novel selenonucleoside suppresses tumor growth by targeting Skp2 degradation in paclitaxel-resistant prostate cancer.

Byun WS, Jin M, Yu J, Kim WK, Song J, Chung HJ, Jeong LS, Lee SK. Byun WS, et al. Among authors: jeong ls. Biochem Pharmacol. 2018 Dec;158:84-94. doi: 10.1016/j.bcp.2018.10.002. Epub 2018 Oct 5. Biochem Pharmacol. 2018. PMID: 30292755

2

Induction of quinone reductase activity by stilbene analogs in mouse Hepa 1c1c7 cells.

Heo YH, Kim S, Park JE, Jeong LS, Lee SK. Heo YH, et al. Among authors: jeong ls. Arch Pharm Res. 2001 Dec;24(6):597-600. doi: 10.1007/BF02975172. Arch Pharm Res. 2001. PMID: 11794542

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: jeong ls. 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. J Med Chem. 2003 Jan 16;46(2):201-3. doi: 10.1021/jm025557z. J Med Chem. 2003. PMID: 12519056

5

Synthesis and biological evaluation of novel apio nucleosides with thiazole-4-carboxamide and 1,2,4-triazole-3-carboxamide.

Kim MJ, Jeong LS, Kim JH, Shin JH, Chung SY, Lee SK, Chun MW. Kim MJ, et al. Among authors: jeong ls. Nucleosides Nucleotides Nucleic Acids. 2004;23(4):715-24. doi: 10.1081/NCN-120037666. Nucleosides Nucleotides Nucleic Acids. 2004. PMID: 15200033

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: jeong ls. 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

A novel adenosine analog, thio-Cl-IB-MECA, induces G0/G1 cell cycle arrest and apoptosis in human promyelocytic leukemia HL-60 cells.

Lee EJ, Min HY, Chung HJ, Park EJ, Shin DH, Jeong LS, Lee SK. Lee EJ, et al. Among authors: jeong ls. Biochem Pharmacol. 2005 Sep 15;70(6):918-24. doi: 10.1016/j.bcp.2005.06.017. Biochem Pharmacol. 2005. PMID: 16051194

On this line, we recently found that a novel adenosine analog, 2-chloro-N6-(3-iodobenzyl)-4'-thioadenosine-5'-N-methyluronamide (thio-Cl-IB-MECA) was a potent human A3AR agonist, and is superior to a known agonist Cl-IB-MECA [Jeong LS, Jin DZ, Kim HO, Shin DH, Moon …

On this line, we recently found that a novel adenosine analog, 2-chloro-N6-(3-iodobenzyl)-4'-thioadenosine-5'-N-methyluronamide (thio-Cl-IB- …

8

Structure-activity relationship of 5'-substituted fluoro-neplanocin a analogues as potent inhibitors of S-adenosylhomocysteine hydrolase.

Moon HR, Lee KM, Lee JH, Lee SK, Park SB, Chun MW, Jeong LS. Moon HR, et al. Among authors: jeong ls. Nucleosides Nucleotides Nucleic Acids. 2005;24(5-7):707-8. doi: 10.1081/NCN-200060286. Nucleosides Nucleotides Nucleic Acids. 2005. PMID: 16248019

9

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. J Med Chem. 2006 Jan 12;49(1):273-81. doi: 10.1021/jm050595e. J Med Chem. 2006. PMID: 16392812

10

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. 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

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