Kim HO - Search Results

1

Structure-activity relationships of 1,3-dialkylxanthine derivatives at rat A3 adenosine receptors.

Kim HO, Ji XD, Melman N, Olah ME, Stiles GL, Jacobson KA. Kim HO, et al. J Med Chem. 1994 Sep 30;37(20):3373-82. doi: 10.1021/jm00046a022. J Med Chem. 1994. PMID: 7932565 Free PMC article.

2

N6-substituted D-4'-thioadenosine-5'-methyluronamides: potent and selective agonists at the human A3 adenosine receptor.

Jeong LS, Jin DZ, Kim HO, Shin DH, Moon HR, Gunaga P, Chun MW, Kim YC, Melman N, Gao ZG, Jacobson KA. Jeong LS, et al. Among authors: kim ho, kim yc. J Med Chem. 2003 Aug 28;46(18):3775-7. doi: 10.1021/jm034098e. J Med Chem. 2003. PMID: 12930138

3

2-Substitution of adenine nucleotide analogues containing a bicyclo[3.1.0]hexane ring system locked in a northern conformation: enhanced potency as P2Y1 receptor antagonists.

Kim HS, Ohno M, Xu B, Kim HO, Choi Y, Ji XD, Maddileti S, Marquez VE, Harden TK, Jacobson KA. Kim HS, et al. Among authors: kim ho. J Med Chem. 2003 Nov 6;46(23):4974-87. doi: 10.1021/jm030127+. J Med Chem. 2003. PMID: 14584948 Free PMC article.

4

Structural determinants of efficacy at A3 adenosine receptors: modification of the ribose moiety.

Gao ZG, Jeong LS, Moon HR, Kim HO, Choi WJ, Shin DH, Elhalem E, Comin MJ, Melman N, Mamedova L, Gross AS, Rodriguez JB, Jacobson KA. Gao ZG, et al. Among authors: kim ho. Biochem Pharmacol. 2004 Mar 1;67(5):893-901. doi: 10.1016/j.bcp.2003.10.006. Biochem Pharmacol. 2004. PMID: 15104242 Free PMC article.

5

Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5'-ribofuran-uronamide moiety.

Gao ZG, Joshi BV, Klutz AM, Kim SK, Lee HW, Kim HO, Jeong LS, Jacobson KA. Gao ZG, et al. Among authors: kim ho, kim sk. Bioorg Med Chem Lett. 2006 Feb;16(3):596-601. doi: 10.1016/j.bmcl.2005.10.054. Epub 2005 Nov 10. Bioorg Med Chem Lett. 2006. PMID: 16289820 Free PMC article.

6

Orthogonal activation of the reengineered A3 adenosine receptor (neoceptor) using tailored nucleoside agonists.

Gao ZG, Duong HT, Sonina T, Kim SK, Van Rompaey P, Van Calenbergh S, Mamedova L, Kim HO, Kim MJ, Kim AY, Liang BT, Jeong LS, Jacobson KA. Gao ZG, et al. Among authors: kim ho, kim sk, kim ay, kim mj. J Med Chem. 2006 May 4;49(9):2689-702. doi: 10.1021/jm050968b. J Med Chem. 2006. PMID: 16640329 Free PMC article.

7

Structure-activity relationships of 9-alkyladenine and ribose-modified adenosine derivatives at rat A3 adenosine receptors.

Jacobson KA, Siddiqi SM, Olah ME, Ji XD, Melman N, Bellamkonda K, Meshulam Y, Stiles GL, Kim HO. Jacobson KA, et al. Among authors: kim ho. J Med Chem. 1995 May 12;38(10):1720-35. doi: 10.1021/jm00010a017. J Med Chem. 1995. PMID: 7752196 Free PMC article.

8

2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptors.

Kim HO, Ji XD, Siddiqi SM, Olah ME, Stiles GL, Jacobson KA. Kim HO, et al. J Med Chem. 1994 Oct 14;37(21):3614-21. doi: 10.1021/jm00047a018. J Med Chem. 1994. PMID: 7932588 Free PMC article.

9

Selective ligands for rat A3 adenosine receptors: structure-activity relationships of 1,3-dialkylxanthine 7-riboside derivatives.

Kim HO, Ji XD, Melman N, Olah ME, Stiles GL, Jacobson KA. Kim HO, et al. J Med Chem. 1994 Nov 11;37(23):4020-30. doi: 10.1021/jm00049a021. J Med Chem. 1994. PMID: 7966162 Free PMC article.

10

Synthesis, biological activity, and molecular modeling of ribose-modified deoxyadenosine bisphosphate analogues as P2Y(1) receptor ligands.

Nandanan E, Jang SY, Moro S, Kim HO, Siddiqui MA, Russ P, Marquez VE, Busson R, Herdewijn P, Harden TK, Boyer JL, Jacobson KA. Nandanan E, et al. Among authors: kim ho. J Med Chem. 2000 Mar 9;43(5):829-42. doi: 10.1021/jm990249v. J Med Chem. 2000. PMID: 10715151 Free PMC article.

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