Gao ZG - Search Results

1

Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N(6)-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonists.

Nayak A, Chandra G, Hwang I, Kim K, Hou X, Kim HO, Sahu PK, Roy KK, Yoo J, Lee Y, Cui M, Choi S, Moss SM, Phan K, Gao ZG, Ha H, Jacobson KA, Jeong LS. Nayak A, et al. Among authors: gao zg. J Med Chem. 2014 Feb 27;57(4):1344-54. doi: 10.1021/jm4015313. Epub 2014 Feb 5. J Med Chem. 2014. PMID: 24456490 Free PMC article.

2

Identification by site-directed mutagenesis of residues involved in ligand recognition and activation of the human A3 adenosine receptor.

Gao ZG, Chen A, Barak D, Kim SK, Müller CE, Jacobson KA. Gao ZG, et al. J Biol Chem. 2002 May 24;277(21):19056-63. doi: 10.1074/jbc.M110960200. Epub 2002 Mar 12. J Biol Chem. 2002. PMID: 11891221 Free PMC article.

3

2-Chloro-N(6)-cyclopentyladenosine, adenosine A(1) receptor agonist, antagonizes the adenosine A(3) receptor.

Gao ZG, Jacobson KA. Gao ZG, et al. Eur J Pharmacol. 2002 May 17;443(1-3):39-42. doi: 10.1016/s0014-2999(02)01552-2. Eur J Pharmacol. 2002. PMID: 12044789 Free PMC article.

4

Selective allosteric enhancement of agonist binding and function at human A3 adenosine receptors by a series of imidazoquinoline derivatives.

Gao ZG, Kim SG, Soltysiak KA, Melman N, IJzerman AP, Jacobson KA. Gao ZG, et al. Mol Pharmacol. 2002 Jul;62(1):81-9. doi: 10.1124/mol.62.1.81. Mol Pharmacol. 2002. PMID: 12065758 Free PMC article.

5

Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist.

Maconi A, Pastorin G, Da Ros T, Spalluto G, Gao ZG, Jacobson KA, Baraldi PG, Cacciari B, Varani K, Moro S, Borea PA. Maconi A, et al. Among authors: gao zg. J Med Chem. 2002 Aug 15;45(17):3579-82. doi: 10.1021/jm020974x. J Med Chem. 2002. PMID: 12166930 Free PMC article.

6

Structural determinants of A(3) adenosine receptor activation: nucleoside ligands at the agonist/antagonist boundary.

Gao ZG, Kim SK, Biadatti T, Chen W, Lee K, Barak D, Kim SG, Johnson CR, Jacobson KA. Gao ZG, et al. J Med Chem. 2002 Sep 26;45(20):4471-84. doi: 10.1021/jm020211+. J Med Chem. 2002. PMID: 12238926 Free PMC article.

7

Differential allosteric modulation by amiloride analogues of agonist and antagonist binding at A(1) and A(3) adenosine receptors.

Gao ZG, Melman N, Erdmann A, Kim SG, Müller CE, IJzerman AP, Jacobson KA. Gao ZG, et al. Biochem Pharmacol. 2003 Feb 15;65(4):525-34. doi: 10.1016/s0006-2952(02)01556-3. Biochem Pharmacol. 2003. PMID: 12566079 Free PMC article.

8

Design, synthesis and binding affinity of 3'-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands.

Lim MH, Kim HO, Moon HR, Lee SJ, Chun MW, Gao ZG, Melman N, Jacobson KA, Kim JH, Jeong LS. Lim MH, et al. Among authors: gao zg. Bioorg Med Chem Lett. 2003 Mar 10;13(5):817-20. doi: 10.1016/s0960-894x(03)00027-1. Bioorg Med Chem Lett. 2003. PMID: 12617898

9

Identification of essential residues involved in the allosteric modulation of the human A(3) adenosine receptor.

Gao ZG, Kim SK, Gross AS, Chen A, Blaustein JB, Jacobson KA. Gao ZG, et al. Mol Pharmacol. 2003 May;63(5):1021-31. doi: 10.1124/mol.63.5.1021. Mol Pharmacol. 2003. PMID: 12695530 Free PMC article.

10

N6-Substituted adenosine derivatives: selectivity, efficacy, and species differences at A3 adenosine receptors.

Gao ZG, Blaustein JB, Gross AS, Melman N, Jacobson KA. Gao ZG, et al. Biochem Pharmacol. 2003 May 15;65(10):1675-84. doi: 10.1016/s0006-2952(03)00153-9. Biochem Pharmacol. 2003. PMID: 12754103 Free PMC article.

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