Gao ZG - Search Results

1

Correction to "Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A_2A/A₃ Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity".

Kim G, Hou X, Byun WS, Kim G, Jarhad DB, Lee G, Hyun YE, Yu J, Lee CS, Qu S, Warnick E, Gao ZG, Kim JY, Ji S, Shin H, Choi JR, Jacobson KA, Lee HW, Lee SK, Jeong LS. Kim G, et al. Among authors: gao zg. J Med Chem. 2024 Feb 8;67(3):2236. doi: 10.1021/acs.jmedchem.3c02442. Epub 2024 Jan 23. J Med Chem. 2024. PMID: 38259147 Free PMC article. No abstract available.

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

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.

5

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.

6

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

7

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.

8

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: gao zg. J Med Chem. 2003 Aug 28;46(18):3775-7. doi: 10.1021/jm034098e. J Med Chem. 2003. PMID: 12930138 Free PMC article.

9

Modeling the adenosine receptors: comparison of the binding domains of A2A agonists and antagonists.

Kim SK, Gao ZG, Van Rompaey P, Gross AS, Chen A, Van Calenbergh S, Jacobson KA. Kim SK, et al. Among authors: gao zg. J Med Chem. 2003 Nov 6;46(23):4847-59. doi: 10.1021/jm0300431. J Med Chem. 2003. PMID: 14584936 Free PMC article.

10

Structure-activity relationships of thiazole and thiadiazole derivatives as potent and selective human adenosine A3 receptor antagonists.

Jung KY, Kim SK, Gao ZG, Gross AS, Melman N, Jacobson KA, Kim YC. Jung KY, et al. Among authors: gao zg. Bioorg Med Chem. 2004 Feb 1;12(3):613-23. doi: 10.1016/j.bmc.2003.10.041. Bioorg Med Chem. 2004. PMID: 14738972 Free PMC article.

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